- Research article
- Open Access
Antidepressants in the treatment of depression/depressive symptoms in cancer patients: a systematic review and meta-analysis
BMC Psychiatry volume 13, Article number: 140 (2013)
Over the past thirty years a number of studies have suggested that antidepressants can be effective in the treatment of depressive symptoms in patients with cancer. The aim of this paper was to review randomized controlled trials (RCTs) and to perform a meta-analysis in order to quantify their overall effect.
Pubmed and the Cochrane libraries were searched for the time period between 1980 and 2010.
Nine RCTs were identified and reviewed. Six of them (with a total of 563 patients) fulfilled the criteria for meta-analysis, but exhibited an unclear risk for bias. The estimated effect size was 1.56 with 95% CI: 1.07- 2.28 (p= 0.021). There were no differences in discontinuation rates between antidepressants and placebo groups (RR= 0.86 with 95% CI 0.47- 1.56, p=0.62).
This meta-analysis suggests that antidepressants can be effective in treating depressive symptoms beside clinical depression. When considering the risk of side effects and interactions and the heterogeneity among the mostly small studies, a general recommendation cannot be made until well-controlled studies are conducted.
The role of depression in physical illness has been recognized and addressed by many authors. Up to one third of physically ill patients attending hospital have depressive symptoms. The diseases with the highest prevalence of major depression have been reported as follows (from higher to lower incidence): inflammatory bowel disease, multiple sclerosis, epilepsy, asthma, back problems, cancer, COPD, migraine, rheumatic arthritis, stroke, Parkinson’s disease, diabetes mellitus, and heart disease . Over the last several years, there has been a growing interest for the psychological aspects of cancer due to its severe impact on quality of life (QOL) [2, 3]. Physical symptoms that are associated with both depression and cancer can be a confounding factor in the assessment of depression in this population . Several studies evaluated the efficacy of psychological and pharmacological interventions in the treatment of depression. The psychopharmacological interventions and particularly the use of antidepressants are systematically reviewed here and meta-analytical methods are applied to quantify their overall effect.
Cancer is associated with depression and depressive symptoms. A meta-analysis by Mitchel et al.  included 94 studies and found that the pooled prevalence of major depression in palliative care settings and haemato-oncological settings was equal to 16.5% (95% CI: 13.1-20.3%) and 16.3% (95% CI: 13.4-19.5%), respectively. Restricting the analysis to standardized clinical assessment, Ng and colleagues  found a prevalence of 10.8% and also a substantial amount of heterogeneity. Even though these rates appear to be high, a consistent difference to a systematically matched sample from general population data is still controversial. The existing data suggest that “survivorship presents ongoing psychological challenges” .
There are two main confounding factors in the assessment of depression in cancer patients. First, the distinction between normal sadness or grief and symptoms indicating a depressive episode is not well-defined. Indeed, a phase of reduced mood or depression is considered part of healthy coping with grief (e.g. Kübler-Ross already in 1969 ). Further, such reaction patterns may recur as the disease progresses, by treatment failure, or by findings of metastases. Therefore, also time criteria may not capture the dynamics of disease progression.
A second confounder is the lack of specificity of the depressive symptoms. The ICD-10 and DSM-IV criteria for depressive episode include symptoms that are often present in patients with cancer as well, e.g. loss of appetite, low energy levels, or sleep disturbance. Therefore, the definition of depression in cancer patients and in physical illness is ambiguous . It is suggested to identify the patients by their symptoms and not by a clinical syndrome because the ability to detect cases of depressive episode or disorder may be less important than the ability to detect depressive symptoms remediable to treatment . Several approaches have been developed to solve the problem of diagnosing depression in cancer patients . For instance, the substitutive approach suggests that all physical/somatic symptoms (change in appetite/weight, sleep disturbance, fatigue, loss of energy, diminished ability to think or concentrate) are replaced by non-somatic symptoms (tearfulness, depressed appearance, social withdrawal, decreased talkativeness, brooding, self-pity, pessimism, lack of reactivity, blunting) . These are known as the Endicott criteria. Therefore, established criteria for depression may not be better suited to detect therapeutic indications in cancer patients than the presence of depressive symptoms.
Many guidelines for the treatment of cancer recommend that all cancer patients should be screened for depression, pain, and fatigue (e.g. by the National Institute of Health ). Multi-item scales are used for screening and diagnosing depression. Quantified results are used to specify the illness severity and to monitor the course of the disease. For detecting depression, ultra brief screening tools have been developed and proven to be reliable. For instance, Chochinov reported that the single question: “Are you depressed?” can be a reliable screening tool . There is clear evidence that the systematic application of screening instruments reduces false negative findings, but the specificity and effects on outcome measures not sufficiently studied .
Depression seems to influence the prognosis and even the survival of cancer patients. For instance, Satin et al. conducted a meta-analysis with 27 studies on mortality in cancer patients and depression. A significant effect of depression on mortality was reported (RR: 1.25, P<0.001). The majority of studies measured the effect of depressive symptoms and only three of them included patients with clinical depression. A correlation with disease severity cannot be excluded . In a large cohort study, patients who had recently received a cancer diagnosis had an increased risk for both suicide and death from cardiovascular causes as compared with controls . Trials found that a decrease in severity of depressive symptoms is associated with a prolongation of survival in cancer patients [17, 18]. However, these findings remain controversial as the majority of studies failed to replicate them [19–22].
Treatment of depression in patients with cancer
The treatment of depression can mainly be divided into two categories: psychosocial and pharmacological interventions. A meta-analysis found that cognitive behavioral therapy has a positive effect on depression and quality of life in patients with cancer. In the same meta-analysis patient education had a positive influence on quality of life but not on depression . A further meta-analysis of psychotherapeutic and psychopharmacological studies found allover positive effects on depression ratings . Meta-analyses focusing on pharmacological treatment give a less consistent picture.
Previous reviews [6, 25–28] underpinned the lack of evidence of the adequate effect of pharmacological interventions in the treatment of depression in cancer patients. However, the reviewed studies were heterogeneous as concerns the studied population (e.g. fatigue or pain as eligibility criterion and depression as secondary outcome) and the type of the drug applied (e.g. antidepressants, benzodiazepines, antipsychotics, psychostimulants, etc.). Only limited conclusions could be drawn from these reviews for the effectiveness of antidepressants in this population. A meta-analysis estimated the efficacy of antidepressants in palliative care (patients with cancer, HIV, COPD, etc.; ). The overall effect of antidepressants was significantly higher than the effect of placebo. However, only four of the twenty-five studies included cancer patients. A subgroup analysis was not performed for each subpopulation and thus no recommendation can be given for oncological patients. In another meta-analysis, antidepressants were found to be effective in the treatment of major depression with a co-morbid physical illness (RR= 1.42, P<0.0001). Again, only four RCTs were included that studied cancer patients with a diagnosis of major depression and no significant effect of antidepressants on response rates emerged in this subpopulation (RR=1.26, P=0.19) . In contrast, Hart et al.  found a significant effect on depression ratings in the subgroup of four pharmacological studies which was not significantly different from the overall effect of the psychotherapeutic trials. However, this analysis included one placebo group twice and used Hedge’s g to quantify the results, which may bias statistics in the pharmacological subgroup. The authors discuss as a limitation that changes in questionnaire ratings may have limited clinical relevance. Depressiveness even without manifest diagnosis of depression may have adverse effects on prognosis and quality of life in cancer patients (see ) and, therefore, these patients should be included in intervention trials and subsequent meta-analyses. To overcome the limitations of the previous analyses, the present systematic review and meta-analysis focuses on the event of clinical relevant symptom changes in depressed or depressive patients with cancer.
The aim of the present study was to determine whether antidepressants are effective in the treatment of depression and depressive symptoms in patients with cancer. The inclusion criteria for the studies were:
Double-blind randomized-controlled trials (RCTs), which could be placebo-controlled or head-to-head trials. For the purposes of the meta-analysis only placebo-controlled trials were used.
The eligibility criteria of the studies were the presence of depression or depressive symptoms in patients with malignancy, i.e. impaired mood had to be diagnosed by clinical criteria or relevant depression rating scales.
The primary outcome of the studies was reduction in severity of depression or depressive symptoms.
The studies were published in English in the time between 01.01.1980 and 31.12.2010.
Antidepressants are often used for indications other than depression (e.g. fatigue, pain, hot flashes) in patients with malignancy. Thus, we excluded all studies, which had depression as a secondary outcome only.
We searched for studies in the electronic databases Pubmed and the Cochrane Library. We aimed towards higher sensitivity and lower precision in this first selection in order not to miss an appropriate study. In particular, we omitted any search term for therapy or treatment, which could reduce the search sensitivity. This approach is suggested by the “Cochrane Handbook for systematic Reviews of Interventions” (§6.4.4) . Search terms were: “(depressive OR depression) AND (cancer OR tumor OR neoplasm OR lymphoma OR leukemia)”. The applied limits of the search were 1. articles should be published in the time between 01.01.1980 and 31.12.2010; 2. articles should be in English language; and 3. the search term appeared in the title or the abstract of the articles. We further searched through the reference lists of reviews and relative articles to identify any additional studies. Exploratory extensions of search terms (e.g. including ‘oncology’) did not yield additional studies.
Article selection and review strategy
The selection of studies involved an initial screening of the title and the abstract in order to find studies, which were appropriate according to the inclusion criteria stated above. If it was not clear from the title or the abstract that the study should be rejected, the full text was obtained. The process was conducted independently by both authors in order to reduce the possibility of relevant articles being rejected.
The data were extracted independently by both authors. In case of disagreement, a clinician experienced in psycho-oncology and liaison psychiatry could be involved to mediate consensual decisions. A structured format was used as the one applied in the presentation of the single studies in the appendix. Dichotomous data were collected for the primary outcomes of this review (responders and non-responders to treatment). Secondary outcomes were the number of drop outs, the number of patients with adverse effects, and the quality of life.
Statistical methods (meta-analysis)
A random effects model was applied in the meta-analysis because of the assumption that the true effect size was not the same in all studies. Indeed, there were marked differences between the studies regarding the type of cancer, the stage of cancer, the drug used in each study, and the design (intention to treat analysis or completers’ analysis). The risk ratio (RR with 95% confidence intervals) was preferred to odds ratio for the computation of the effect size because it has the advantage of being more intuitive . Heterogeneity I2 was computed in order to assess the percentage of the overall variability attributed to the between studies variability.
The risk of bias in individual studies was evaluated using the Cochrane Collaboration’ s domain based tool which assesses allocation concealment, sequence generation, blinding, selective outcome reporting, and other sources of bias. Risk of publication bias was assessed using a funnel plot, i.e. a display of estimated study quality in terms of standard error and the reported effect size. The calculations were performed using standard formulas  in MicroSoft Excel (Excel 2003 Edition, MicroSoft, Redmond, CA). The statistical program “Comprehensive meta-Analysis” (2nd version, Biostat, Englewood, NJ) was used to create forest and funnel plots.
The electronic searches yielded 5959 references from MEDLINE and 1041 references (clinical trials) from the Cochrane Library. After the initial scanning of the abstracts, a total of 38 reports were detected that may relate to drug trials using anti-depressants. Based on the full-text of these reports, 29 of them were rejected since they did not reported RCTs on anti-depressant treatment in depressive cancer patients Figure 1. From the remaining 9 RCTs, 3 studies were head-to-head trials, i.e. active drugs were compared with each other [33–35]. Thus in total 6 randomized placebo-controlled studies fulfilled the criteria for this meta-analysis [36–41]. Table 1 provides an overview of the reviewed studies. The complete list of the assessed trials is presented in Appendix A.
Previous reviews and meta-analyses exhibited a larger diversity of study designs [25–28]. For instance, we did not include 3 trials that had not depression or depressive symptoms as an eligibility criterion even though the primary outcome measure was improvement in depression/depressive symptoms [42–44]. Similarly, we did not include trials which tested the efficacy of antidepressants in preventing depressive symptoms in patients with cancer  or in patients with melanoma undergoing therapy with interferon . Appendix D lists all the 38 trials, which were screened and the reasons for in- or excluding them.
Review of RCTs in depression
Holland et al.  studied 38 patients with depression and breast cancer. The selective serotonine reuptake inhibitor (SSRI) fluoxetine was not found to be superior to the tricyclic antidepressant (TCA) desipramine. Similarly, Pezella et al.  found no significant differences in efficacy between paroxetine (SSRI) und amitryptiline (TCA) in a sample of 185 patients with breast cancer. In contrast, the noradrenergic and specific serotonergic antidepressant (NaSSA) mirtazapine had a larger effect on depression than imipramine in a sample of 53 cancer patients with depression (Cancurtaran et al. 2008; ).
Costa et al.  and van Heeringen et al.  compared the tetracyclic antidepressant mianserin with placebo in 73 and 55 patients with gynecological tumors, respectively. Both publications reported a significant effect on the observed depressive symptoms. In contrast, a trial by Razavi et al.  in 91 patients with various types of cancer did not reveal a significant difference between fluoxetine and placebo. Similarly, Fisch et al.  failed to demonstrate an advantage of fluoxetine over placebo in a sample of 163 patients with advanced cancer. A reevaluation of the results of the former study with the generalized estimating equation (GEE) method of regression suggested a significant effect of the verum as well. Navari et al.  found a significant effect of fluoxetine in 193 depressive patients with breast cancer. Finally, Musselmann et al.  could not document a drug effect in a trial with a small number of patients (n= 35) and 3 groups (paroxetine, desipramine, placebo). For the purposes of the current meta-analysis, we created a combined intervention group, which included the patients from both the paroxetine and the desipramine group, as recommended in the Cochrane handbook .
All studies defined a measure of response, i.e. what was considered a meaningful improvement of the depressive symptoms. The overall effect size in the analysis is RR=1.56 with 95%-CI: 1.07-2.28 (p= 0.021), i.e. under the antidepressants a therapeutic response (as defined in the considered studies) is about 50% more likely than in the placebo group (see Table 2). A graphical display of the relative strength of each study is presented in the forest plot (Figure 2). Four studies found a positive effect of the antidepressants on depressed cancer patients. In the other two studies no significant difference emerged but the 95% confidence intervals were wider than those of the four other studies (Figure 1). This can be considered as indicative of low precision in the trials with negative finding.
The meta-analysis revealed a substantial heterogeneity I2= 71% with 95% CI: 54%-82%. For a substantial I2 (50-90%), the “Cochrane Handbook for systematic Reviews of Interventions”  recommends a reanalysis without the outlying studies as part of a sensitivity analysis. Indeed, the RR of the study by Navari et al.  is much higher than all other values (see Figure 2) and the analyses were repeated excluding this study. The effect of the antidepressants remained significantly better in comparison to placebo after excluding the outlying study (RR = 1.39, 95%-CI: 1.09- 1.77, p = 0.008) and the heterogeneity decreased to 10% (95%-CI 0-22%). Heterogeneity between 0% and 40% is considered to be of no importance . This finding confirms that the high heterogeneity is most likely due to one outlier which however does not bias the finding.
Four factors differentiating the studies were identified post-hoc. The selected predictors were: 1. depression vs. depressive symptoms as eligibility criteria; 2. analysis on an intention-to-treat (ITT) basis vs. completers’ analysis; 3. inclusion of all or only advanced cancer stages vs. inclusion of only early stages; and 4. the substance group SSRI vs. tetracyclic antidepressants (mianserin). In this post-hoc analysis, mianserin had significantly higher RR for responders than the SSRIs (RRSSRI = 1.16, RRmianserin = 1.67, Zdifference = -2.17, p = 0.03). In this latter subgroup comparison, only the paroxetine group from the study by Musselmann et al. was contrasted in order to make the intervention groups comparable. The other predictors did not significantly influence the RR for antidepressant effects. Appendix C provides the details of the subgroup analysis.
Adverse effects and dropouts
There was a substantial amount of missing data concerning the adverse effects in these studies. Only three studies reported the total number of patients with side effects. Four studies provided data about the number of drop outs because of side effects in each arm (Table 3). Visual inspection suggested no difference. However due to missing data, we did not perform a meta-analysis for the adverse effects. All but one studies provided information about the number of dropouts in each arm (Table 4). We performed a meta-analysis using relative risk ratios and found no significant difference between dropouts in the verum and placebo groups (mean RR = 0.86, 95%-CI 0.47- 1.56, p = 0.62).
Quality of life
Only three of the six studies included an outcome measure for quality of life. Razavi et al.  used the Spitzer Quality of Life Index (SQOLI). The increase in the SQOLI scores was significant in both the drug and the placebo group, but the difference between the two groups was not statistically significant. Fisch et al.  used the Functional Assessment of Cancer Therapy-General (FACT-G, version 3). There was no significant difference between the fluoxetine and the placebo group in the proportion of responders (six points change). Using the generalized estimating equations (GEE) method of regression (post-hoc), there was a significant improvement in the total FACT-G scores in the fluoxetine group compared with placebo. Navari et al.  also used the FACT-G scale. The number of patients who had a significant improvement in quality of life was statistically significantly higher in the fluoxetine group as compared to the placebo group.
Risk for bias and publication bias
The risk of bias for each study can be determined by assessing the following six domains: 1. sequence generation, 2. allocation concealment, 3. blinding, 4. missing data, 5. selective outcome reporting, and 6. other sources of bias . The group of studies was relative homogenous and the overall risk for bias could be described as “unclear” (Figure 3). The results for every single trial are presented in the Appendix B. The risk for publication bias (i.e. studies with small sample size are more likely not to be published if their effect is small to moderate) is assessed by means of the funnel plot, which displays the relationship between the sample size and the effect size of the studies. The standard error instead of the sample size is usually used in the Y axis. No indication for publication bias can be derived from the present funnel plot; in particular, there was no gap on the bottom left side, which would be indicative of unpublished studies with small to moderate effects (Figure 4).
This is the first systematic review with meta-analysis which focuses exclusively on the psychopharmacological treatment in cancer patients with depression. Treatment with SSRI or tetracyclic antidepressants was found to improve depressive symptoms more than placebo. The small number of studies and patients included, as well as the questionable risk of bias, however, points out the demand for well-conducted trials before general recommendations can be derived. The diagnosis and treatment of depression is of high importance in this population of patients because of the high risk for suicide , its impact on the quality of life [2, 3], and its influence on anticancer treatment adherence and compliance . Critical for an antidepressive treatment in this group of patients is a well-funded base of evidence since elevated risks of adverse effects and interactions must be expected (see adverse effects and side effects below). Interestingly in some cancer patients, subsyndromal depressive symptoms (with DSM-IV or ICD-10 diagnosis) may improve under the antidepressants as well. Direct comparisons between classical tricyclic antidepressants and SSRIs revealed no differences in two of the three reviewed head-to-head trials. The higher effect size of the tetracyclic agent mianserin in comparison to SSRIs – as seen in the subgroup analysis – must therefore be considered exploratory. At this point no specific recommendation concerning effectiveness for a substance class can be made.
Several studies and meta-analyses have reported on the effectiveness of antidepressants in patients with depression and physical illness. Van der Feltz-Cornelis et al.  showed in a meta-analysis that pharmacological interventions are effective in reducing depressive symptoms in patients with diabetes mellitus. Price et al.  found in another meta-analysis a significant effect of antidepressants in treating depression in patients with neurological disorders. There are RCTs which show a positive effect of SSRIs on depression in patients with asthma [50, 51]. SSRIs were also found to be effective in the treatment of depression in patients with coronary artery disease . Although the prevalence of depression in patients with inflammatory bowel disease (IBD) is high , there are no RCTs which assess the treatment of depression in this population .
Depression and depressive symptoms
There is a trend towards identifying depressive symptoms instead of trying to define exact diagnoses of concrete depressive syndromes [9, 10]. There are also many simple single- or two-item screening tools, which can detect depression with high specificity and sensitivity. As shown in the subgroup analysis, patients with depressive symptoms can benefit from the use of antidepressants exactly like the patients diagnosed with major depression. On the one hand, this conclusion is of significant clinical importance because it addresses a practical issue and can motivate physicians to screen for depression with simple and easy to use tools. On the other hand, it must be taken into consideration that there was only one study in one of the two compared groups in the subgroup analysis . The authors of this study reported a better response in the patients who had a score higher than 4 in the TQSS, suggesting that a minimum of symptom severity may be required for the antidepressive action of antidepressants. Thus, the results of the subgroup analysis should be interpreted very carefully and not be misinterpreted as an excuse for an unreasonable use of antidepressants by physicians or for the limitation of the role of the consultation-liaison psychiatry in oncology.
Side effects and interactions
When using an antidepressant, one should pay attention on possible side effects such as pro-emetic effects of SSRIs and anticholinergic effects of TCA. Nausea is a common adverse effect among cancer patients undergoing chemotherapy and can be worsened by SSRIs. Cognitive impairment or acute psychiatric conditions such as delirium can also get worse through the anticholinergic properties of TCAs. Adverse effects such as agranulocytosis with mianserin  should be taken into consideration in the treatment of cancer patients who receive chemotherapy.
There are also many interactions between antidepressants and drugs used in the treatment of cancer. The best studied interactions are these between SSRIs and tamoxifen (a Selective Estrogen Receptor Modulator or SERM), which is metabolized by CYP2D6 into its active form endoxifen . Antidepressants such as paroxetine and duloxetine can inhibit the CYP2D6 cytochrome and thus the formation of the active metabolite endoxifen .
The heterogeneity between studies was substantial (I2= 71% with 95% CI: 54%-82%). As recommended in the Cochrane guidelines (see above), the meta-analysis was recalculated excluding an outlying value (as part of a sensitivity analysis). The efficiency remained significant even after removing an extreme high value (M*= 1.39, p= 0.008). The heterogeneity fell to 10% which is considered to be of no importance. Thus, heterogeneity affects psychopharmacological studies in cancer patients. Nevertheless, the overall therapeutic effects seem to be consistent across studies.
The reliability of these results is limited by the small number of randomized controlled studies. A larger number of studies are needed to get safe conclusions. The small number of studies and participants can be attributed among other reasons to the preference of the patients and the clinicians for non-blinded treatment, as reported by Musselmann et al. . This may explain the large number of open label studies found in the search in the databases (which are not presented here). Another factor which limits the validity of our results is the quality of the studies. The average risk for bias in these studies could be described as “unclear.” As shown in the risk for bias graph (Figure 3), the group of studies was relatively homogenous as regards to this issue. Other limitations of this meta-analysis are the use of different depression rating scales and the different response criteria used by the authors.
Considering the high prevalence of depression and its impact on mortality and quality of life in cancer patients, it is a matter of concern that only a few trials assessing antidepressant efficacy are available. Given this limitation, we found that antidepressants are effective in the treatment of depression or depressive symptoms in patients with cancer. A minimum of depressive symptoms’ severity may be required for the patients to benefit from the use of antidepressants. Though a larger effect size of mianserin in comparison to SSRIs in the subgroup analysis has been shown, no recommendation can be made for one antidepressant type over another. A quantification of tolerability, as ascertained by comparing the number of patients with adverse effects, was not possible because of the missing data. The number of drop outs did not differ significant between the intervention and the control group.
There are difficulties in defining the diagnosis of clinical depression in cancer patients. Symptoms such as fatigue, sadness, worry, and pain are reported by depressed patients as well as in patients with advanced disease. Practical issues such as the ability of physicians to recognize patients with depression should also be considered. Reliable single- or two-item questionnaires have been developed for this purpose. The detection of depressive symptoms might be more important than the exact diagnosis of clinical depression. The current meta-analysis suggests further that antidepressants could be effective in treating sub-clinical depression. However, studies with larger samples are needed in order to verify such conclusion before general clinical recommendations can be derived.
Listing of the studies
After scanning 7,000 references and screening 38 articles that seemed appropriate 9 trials could be identified to fulfill the study inclusion criteria. They were further categorized into 2 clusters:
Three RCTs compared two antidepressants with each other (head-to-head trials). These studies did not include a placebo control group.
Holland et al., 1998
Number of patients: 40 patients were recruited and 38 ones of these were randomized (21 patients to the fluoxetine and 17 to the desipramine group).
Type of cancer/Stages: Breast cancer. Stages: II, III, IV.
Duration: six weeks
Evaluation tools: the Hamilton Depression Rating Scale (17 item HAM-D), the Clinical and Patient’s Global Impression scales (CGI and PGI), the Hamilton Anxiety Rating scale (HAM-A), the Functional Living Index for Cancer (FLIC), the Memorial Pain Assessment Card (MPAC) and the SF-36 Health Survey.
Inclusion criteria: Major depressive episode or adjustment disorder with depressed mood and scores over 14 on the first 17 items of HAM-D.
Response criteria: a statistically significant baseline to endpoint change in HAM-D.
Design: double blind RCT with ITT analysis, LOCF approach.
Results: There was a significant improvement in the HAM-D scores in both group as evidenced by baseline-to-endpoint changes (p<0.001). ANOVA showed no significant difference between fluoxetine and desipramine. Similar improvement was also observed in the HAM-A. There were no significant differences in the dropout rates in the fluoxetine and desipramine group (28.6% and 41.2%, respectively). The only adverse effect revealing a significance difference was dry mouth reported by 14 (66.6%) patients in the fluoxetine group and 4 (23.5%) patients in the desipramine group.
Pezzela et al., 2001
Number of patients: 179 patients were randomized into either the paroxetine group (n= 89) or the amitiptyline group (n=90). 88 patients from the first and 87 from the second group received medication and were included in the ITT analysis.
Type of cancer/Stages: Breast cancer, any stage.
Duration: eight weeks
Evaluation tools: Montgomery and Asberg Depression Rating Scale (MADRS), the Clinical Global Impression (CGI), the functional living index: cancer (FLIC) and the patient’s global evaluation (PGE).
Inclusion criteria: The patients should fulfill the ICD-10 criteria for depressive episode and have a minimum score of 16 in the MADRS.
Response criteria: At least 50% decrease from baseline in MADRS score
Design: double blind RCT, ITT analysis, LOCF approach.
Results: 38 patients in the paroxetine group (43.7%) and 33 patients in the amitriptyline group (37.8%) were responders (p= 0.441). 47 patients in the first and 53 from the second group reported at least one adverse experience. There were 16 withdrawals in the paroxetine group and 19 withdrawals in the amitriptyline group. The study showed that paroxetine and amitriptyline were similar in efficacy and tolerability.
Cancurtaran et al., 2008
Number of patients: 53 patients participated in this study: 20 patients in the mirtazapine group, 13 patients in the imipramine group and 20 patients in a control group without medication or placebo (only supportive psychotherapy).
Type of cancer/Stages: The type and stage of cancer are not further specified.
Duration: six seeks
Evaluation tools: The patients were screened with the Structured Clinical Interview for Diagnostic (SCID). The Hospital Anxiety and Depression Scale (HADS) was administered for assessment of depression and anxiety during the study.
Inclusion criteria: Major depressive disorder, adjustment disorder, anxiety disorders.
Response criteria: The authors reported on the statistical significance of the rating differences between baseline and endpoint in each group.
Design: double blind RCT (not blinded for those who denied medication and received only psychotherapy), completers’ analysis.
Results: The patients in the mirtazapine group improved significantly after the six weeks in the total HADS scores (p=0.014), the anxiety subscale (p=0.04) and the depression subscale (p=0.008). The patients in the other two groups did not show any significant improvement.
B. Placebo controlled trials
The pharmacological agents that were used in these six studies were: mianserin (two trials), fluoxetine (three trials) and paroxetine (one trial). Musselman et al. used an additional third group with cancer patients receiving desipramine.
Costa 1985 and van Heeringen 1996 compared mianserin with placebo. Both reported a significant improvement of the depressive symptoms. Mianserin is a tetracyclic antidepressant agent and is considered as the predecessor of mirtazapine.
Costa et al., 1985
Number of patients: 73 patients participated in this study (36 in the drug group and 37 in the placebo group).
Type of cancer/Stages: Gynecological cancers, stages II, III, IV
Duration: four weeks
Screening/Evaluation tools: Zung Self-Rating Depression Scale (ZSRDS), Hamilton Depression Rating Scale. Secondary tools measures: Clinical Global Impression of Illness Severity (CGI-S).
Inclusion Criteria: ZSRDS over 41 and HDRS score over 16.
Response criteria: nor reported.
Design: Double blind RCT, ITT analysis, LOCF approach.
Results: 28 of the 36 patients of the mianserin group were responders. There were only 18 responders among the 37 participants in the placebo group (response evaluated according to the CGI scores). This difference was statically significant (P<0.025, Chi squared= 6.62). The primary outcome was based on the scores of HDRS. There were 7 dropouts in the mianserin group and 15 in the placebo group. 17 patients from the drug group and 11 from the placebo group reported side effects. This difference was not statistically significant (Chi squared = 2.11).
Van Heeringen and Zivkov, 1996
Number of patients: 55 participants in the study (28 in the mianserin group and 27 in the placebo group)
Type of cancer/Stages: Breast cancer. Stages I, II
Duration: 7 weeks
Screening tool: Hamilton Depression Rating Scale (HDRS)
Inclusion Criteria: HDRS score over 16
Response criteria: 50% decrease in baseline HRDS scores
Design: double blind RCT, ITT analysis, LOCF approach.
Results: 19 patients from the 28 ones in the mianserin group and 10 patients from the 27 ones in the placebo group were responders. This difference was statistically significant (p=0.044, Fisher’s exact test). Significantly more placebo treated patients (n=15) than mianserin treated patients (n=6) terminated prematurely the study (P=0.014, Fisher’s exact test). No significant differences were found between numbers of patients complaining of at least one adverse effect (AE) at any assessment point. At day 42, 11 mianserin- and 17 placebo- treated patients reported AEs (P=0.14).
Three RTCs compared fluoxetine with placebo.
Razavi et al., 1996
Number of patients: 91 patients participated in this study (45 in the fluoxetine group and 46 in the placebo group)
Type of cancer/Stages: Any kind of cancer (mainly gynecological), any stage (95% without metastases).
Duration: five weeks
Screening tool: Hospital Anxiety and Depression Scale (HADS). Other measures: the Montgomery and Asberg Depression Scale (MADRS), the Hamilton Anxiety Scale (HAS), the revised Symptom Checklist (SCL-90R) and the Spitzer Quality of Life Index (SQOLI).
Inclusion Criteria: a HADS score over 13
Response criteria: a 50% decrease or more in the baseline HADS scores
Design: double blind RCT, completers’ analysis.
Results: The HADS response rates were 18% in the fluoxetine group and 20% in the placebo group. The success rates (HADS scores under 8 at the end of the trial) were 11% (5 patients) and 7% (3 patients) in the drug and placebo group respectively. As a secondary outcome the author reported the response rates in both groups according to MADRS scale (50% improvement): these were 31% (14 patients) for the fluoxetine group and 33% (15 patients) in the placebo group. These differences were not statistically significant. Significantly more drop outs were observed in the drug group (n=15) than in the placebo group (n=7) (Chi Square test; P=0.04). 67% from the fluoxetine group reported at least one AE compared to 59% in the placebo group (not statistically significant difference: P= 0.43).
Fisch et al., 2003
Number of patients: 163 patients participated in the study (83 patients in the fluoxetine group and 80 patients in the placebo group).
Type of cancer/Stages: Any type of cancer in advanced stage.
Duration: twelve weeks
Screening tool: The Two Question Screening Survey (TQSS) was used to assess mood and anhedonia. The two questions are: “During the past month have you been bothered by feeling down, depressed or hopeless?” and “During the past month have you been bothered by having little interest or pleasure in doing things?” There are five possible answers which are assigned values from 0 to 4:
0 not at all, 1 a little bit, 2 somewhat, 3 quite a bit, 4 very much.
For the evaluation of depression and quality of life in the participants the following tools were used: the Functional Assessment of Cancer Therapy General instrument (FACT-G), the Functional Assessment of Chronic Illness Therapy Spiritual and the Brief Zung Self administered Depression Rating Scale (BZDRS) with 11 items.
Inclusion Criteria: A TQSS score of 2 or greater. Patients with a major depressive episode were excluded.
Response criteria: A best change score of at least -3 in the BZDRS. A best change score is defined as the difference between the baseline score and the average of the best consecutive scores.
Design: Double blind RCT. Computations were made only on patients who completed the baseline questionnaires (n=159) and at least one follow up assessment (n=129). The authors used additionally the generalized estimating equation (GEE) method of regression.
Results: There were data for 129 patients at the end point (64 in the fluoxetine group and 65 in the placebo group). 48% (n=31) patients in the fluoxetine group and 36% (n=23) in the placebo group were responders. This difference was not statistically significant. Reevaluating the data with the GEE method of regression the authors found a significant improvement in the fluoxetine group. There were not any concrete data about the number of dropouts or reported adverse effects in each group.
Navari et al., 2008
Number of patients: 203 patients out of the 357 screened patients qualified for enrolment in this study. From the 193 who enrolled in the study the authors reported on the 180 patients who completed the six month assessment.
Type of cancer/Stages: Breast cancer, stages I, II
Duration: six months
Screening tool: The Two Question Screening Survey (TQSS) was used to assess mood and anhedonia. The two questions are: “During the past month have you been bothered by feeling down, depressed or hopeless?” and “During the past month have you been bothered by having little interest or pleasure in doing things?” There five possible answers which are assigned values from 0 to 4:
0 not at all, 1 a little bit, 2 somewhat, 3 quite a bit, 4 very much.
The quality of life was estimated using the Functional Assessment of Cancer Therapy-General (FACT-G) and the depression was estimated with the Brief Zung self administered Depression Rating Scale (BZDRS).
Inclusion Criteria: A TQSS score of 2 or greater. Patients with a major depressive episode were excluded.
Response criteria: “significant improvement” in the BZSRS (not further defined).
Design: double blind RCT, completers’ analysis.
Results: 71 patients from the fluoxetine group and 23 patients from the placebo group had a significant improvement in depressive symptoms (P<0.0005). There were not any data about adverse effects.
One study compared paroxetine with desipramine and placebo in depressed cancer patients.
Musselman et al., 2006
Number of patients: 35 patients participated in this study. They were divided into three groups and assigned to receive either paroxetine (n=13) or desipramine (n=11) or placebo (n=11).
Type of cancer/Stages: Breast cancer at any stage.
Duration: six weeks
Screening tool: a DSM-III-R multi-axial evaluation. Other rating scales used were the 21-item Hamilton Rating Scale for Depression (HAM-D), the 14-item Hamilton Rating Scale for Anxiety and the Clinical Global Impression Scale (CGI).
Inclusion Criteria: DSM-III-R criteria for major depression (except duration of illness had to be at least on month), HAM-D score of at least 14 in the first 17 items of the 21-item HAM-D.
Response criteria: A decrease of ≥50% from baseline HAM-D score or a CGI global improvement score ≤-2. Clinical remission was defined as a HAM-D score ≤7.
Design: double blind RCT, ITT analysis, LOCF approach
Results: The response rates were: 38% (5/13 patients) in the paroxetine group, 45% (5/11 patients) in the desipramine group and 55% (6/11 patients) in the placebo group (p= 0.91). The remission rates were: 23% (3/11 patients) in the paroxetine group, 45% (5/11 patients) in the desipramine group and 36% (4/11 patients) in the placebo group (p=0.55). There were 14 dropouts by week six: 5 in the paroxetine group, 4 in the desipramine group and 5 in the placebo group.
The most common adverse effects were:
Paroxetine: dry mouth (n=6), nausea (n=5), pain (n=5)
Desipramine: dry mouth (n=8), constipation (n=4), headaches (n=4), pain (n=4)
Placebo: headache (n=5), pain (n=5), dry mouth (n=3), constipation (n=3).
The difference in side effects among the groups was not significant.
Assessment of bias
We used the Cochrane Collaboration’s tool for assessing the risk of bias. These criteria may be considered sufficiently strict. This included extracting of six domains and judging them. The consensual authors’ judgment were either “Yes”, indicating low risk of bias, “No” indicating high risk of bias, or “Unclear” indicating unknown risk of bias. The criteria to assess the studies were: (Tables 5, 6, 7, 8, 9, 10, 11, 12, 13, 14).
In summary, only one study (Fisch et al., 2003) described the exact randomization method. The rest studies defined themselves as randomized, but did not describe the method (“Unclear”). The exact allocation concealment method was not described in any study. All studies were defined as double blind. No article reported which persons in the study were blinded and which were not. All but one studies described an inappropriate missing data imputation method, even the ones who used an ITT-based analysis; the LOCF method can also introduce bias (see Cochrane  and http://www.missingdata.org.uk). In total several indications for Risk of Bias can be observed and most items remained unclear (see Figures 3 and 5).
Subgroup analysis after outlier exclusion
1. Eligibility criteria: Depression vs. depressive symptoms
Subgroup analysis for inclusion criteria (Table 15).
2. Study design: Intention to treat vs. completers’ analysis
Subgroup analysis for study design (ITT vs. completers’ analysis) (Table 16)
3. Eligibility criteria: Cancer stage
Subgroup analysis for cancer stage (Table 17).
4. Comparison between SSRIs and tetracyclic antidepressants
Subgroup analysis for type of antidepressant (Table 18)
List of the final 38 studies (Table 19)
Ruttley A, Reid S: Depression in physical illness. Clin Med. 2006, 6: 533-536. 10.7861/clinmedicine.6-6-533.
Kroenke K, Theobald D, Wu J, Loza JK, Carpenter JS, Tu W: The association of depression and pain with health-related quality of life, disability, and health care use in cancer patients. J Pain Symp Manag. 2010, 40: 327-341. 10.1016/j.jpainsymman.2009.12.023.
Brown LF, Kroenke K, Theobald D, Wu J, Carpenter JS, Tu W: The association of depression and anxiety with health-related quality of life in cancer patients with depression and/or pain. Psychooncology. 2010, 19: 734-741.
House A: Mood disorders in the physically ill–problems of definition and measurement. J Psychosom Res. 1988, 32: 345-353. 10.1016/0022-3999(88)90017-7.
Mitchel AJ, Chan M, Bhatti H, Halton M, Grassi L, Johannen C, Meader N: Prevalence of depression, anxiety, and adjustment disorder in oncological, haematological, and palliative care settings: a meta-analysis of 94 interview-based studies. Lancet Oncol. 2011, 12: 160-174. 10.1016/S1470-2045(11)70002-X.
Ng CG, Boks MP, Zainal NZ, de Wit NJ: The prevalence and pharmacotherapy of depression in cancer patients. J Affect Disord. 2011, 131: 1-7. 10.1016/j.jad.2010.07.034.
Punekar RS, Short PF, Moran JR: Use of psychotropic medications by US cancer survivors. Psychooncology. 2012, 21: 1237-1243. 10.1002/pon.2039.
Kübler-Ross E: On Death and Dying. 1969, New York: Simon & Schuster/Touchstone
Rayner L, Loge JH, Wasteson E, Higginson IJ: EPCRC, European Palliative Care Research Collaborative. The detection of depression in palliative care. Curr Opin Support Palliat Care. 2009, 3: 55-60. 10.1097/SPC.0b013e328326b59b.
Lederberg MS: Psychooncology. Kaplan and Sadock, Textbook of Psychiatry, Volume 2. 2005, Philadelphia: Lippincott Williams and Wilkins, 2225-8
Endicott J: Measurement of depression in patients with cancer. Cancer. 1984, 53: 2243-2248.
Unützer J, Vernon SW, Patrick DL, Ferketich SL, Frame PS, Harris JJ, Hendricks CB, Levin B, Link MP, Lustig C, McLaughlin J, Ried LD, Turrisi AT, National Institutes of Health State-of-the-Science Panel: National institutes of health state-of-the-science conference statement: symptom management in cancer: pain, depression, and fatigue, July 15–17, 2002. J Natl Cancer Inst. 2003, 95: 1110-7.
Chochinov HM, Wilson KG, Enns M, Lander S: Are you depressed? Screening for depression in the terminally ill. Am J Psychiatry. 1997, 154: 674-676.
Carlson LE, Waller A, Mitchell AJ: Screening for distress und unmet needs in patients with cancer: review and recommendations. J Clin Oncol. 2012, 30: 1160-1177. 10.1200/JCO.2011.39.5509.
Satin JR, Linden W, Phillips MJ: Depression as a predictor of disease progression and mortality in cancer patients: a meta-analysis. Cancer. 2009, 115: 5349-5361. 10.1002/cncr.24561.
Fang F, Fall K, Mittleman MA, Sparén P, Ye W, Adami HO, Valdimarsdóttir U: Suicide and cardiovascular death after a cancer diagnosis. New Engl J Med. 2012, 366: 1310-1318. 10.1056/NEJMoa1110307.
Andersen BL, Yang HC, Farrar WB, Golden-Kreutz DM, Emery CF, Thornton LM, Young DC, Carson WE: Psychologic intervention improves survival for breast cancer patients: a randomized clinical trial. Cancer. 2008, 113: 3450-3458. 10.1002/cncr.23969.
Giese-Davis J, Collie K, Rancourt KM, Neri E, Kraemer HC, Spiegel D: Decrease in depression symptoms is associated with longer survival in patients with metastatic breast cancer: a secondary analysis. J Clin Oncol. 2011, 29: 413-420. 10.1200/JCO.2010.28.4455.
Spiegel D, Butler LD, Giese-Davis J, Koopman C, Miller E, DiMiceli S, Classen CC, Fobair P, Carlson RW, Kraemer HC: Effects of supportive-expressive group therapy on survival of patients with metastatic breast cancer: a randomized prospective trial. Cancer. 2007, 110: 1130-1138. 10.1002/cncr.22890.
Kissane DW, Love A, Hatton A, Bloch S, Smith G, Clarke DM, Miach P, Ikin J, Ranieri N, Snyder RD: Effect of cognitive-existential group therapy on survival in early-stage breast cancer. J Clin Oncol. 2004, 22: 4255-4260. 10.1200/JCO.2004.12.129.
Kissane DW, Grabsch B, Clarke DM, Smith GC, Love AW, Bloch S, Snyder RD, Li Y: Supportive-expressive group therapy for women with metastatic breast cancer: survival and psychosocial outcome from a randomized controlled trial. Psychooncology. 2007, 16: 277-286. 10.1002/pon.1185.
Goodwin PJ, Leszcz M, Ennis M, Koopmans J, Vincent L, Guther H, Drysdale E, Hundleby M, Chochinov HM, Navarro M, Speca M, Hunter J: The effect of group psychosocial support on survival in metastatic breast cancer. N Engl J Med. 2001, 345: 1719-1726. 10.1056/NEJMoa011871.
Osborn RL, Demoncada AC, Feuerstein M: Psychosocial interventions for depression, anxiety, and quality of life in cancer survivors: meta-analyses. Int J Psychiat Med. 2006, 36: 13-34. 10.2190/EUFN-RV1K-Y3TR-FK0L.
Hart SL, Hoyt MA, Diefenbach M, Anderson DR, Kilbourn KM, Craft LL, Steel JL, Cuijpers P, Mohr DC, Berendsen M, Spring B, Stanton AL: Meta-analysis of efficacy of interventions for elevated depressive symptoms in adults diagnosed with cancer. J Natl Cancer Inst. 2012, 104: 990-1004. 10.1093/jnci/djs256.
Pirl WF: Evidence report on the occurrence, assessment and treatment of depression in cancer patients. J Natl Cancer Inst Monogr. 2004, 32: 32-39.
Rodin G, Lloyd N, Katz M, Green E, Mackay JA, Wong RKS: Supportive care guidelines group of cancer care ontario program in evidence-based care: the treatment of depression in cancer patients: a systematic review. Support Care Cancer. 2007, 15: 123-136. 10.1007/s00520-006-0145-3.
Williams S, Dale J: The effectiveness of treatment for depression/depressive symptoms in adults with cancer: a systematic review. Br J Cancer. 2006, 94: 372-390. 10.1038/sj.bjc.6602949.
Li M, Fitzgerald P, Rodin G: Evidence-based treatment of depression in patients with cancer. J Clin Oncol. 2012, 30: 1187-1196. 10.1200/JCO.2011.39.7372.
Rayner L, Price A, Evans A, Valsraj K, Hotopf M, Higginson IJ: Antidepressants for the treatment of depression in palliative care: systematic review and meta-analysis. Palliat Med. 2011, 25: 36-51. 10.1177/0269216310380764.
Iovieno N, Tedeschini E, Ameral VE, Rigatelli M, Papakostas GI: Antidepressants for major depressive disorder in patients with a co-morbid axis-III disorder: a meta-analysis of patient characteristics and placebo response rates in randomized controlled trials. Int Clin Psychopharmacol. 2011, 26: 69-74. 10.1097/YIC.0b013e328340775e.
Higgins JPT, Green S: Cochrane Handbook for Systematic Reviews of Interventions 4.2.6 [updated September 2006]. The Cochrane Library Volume, Issue 4. 2006, Chichester, UK: John Wiley & Sons, Ltd
Borenstein M, Hedges RV, Higgins JPT, Rothstein HR: Introduction to Meta-Analysis. 2009, West Sussex: Wiley Edition
Holland JC, Romano SJ, Heiligenstein JH, Tepner RG, Wilson MG: A controlled trial of fluoxetine and desipramine in depressed women with advanced cancer. Psychooncology. 1998, 7: 291-300. 10.1002/(SICI)1099-1611(199807/08)7:4<291::AID-PON361>3.0.CO;2-U.
Pezella G, Moslinger-Gehmayr R, Contu A: Treatment of depression in patients with breast cancer: a comparison between paroxetine and amitrptyline. Breast Cancer Res Treat. 2001, 70: 1-10. 10.1023/A:1012518831494.
Cankurtaran ES, Ozalp E, Soygur H, Akbiyik DI, Tuhan L, Alkis N: Mirtazapine improves sleep and lowers anxiety and depression in cancer patients: superiority over imipramine. Support Care Cancer. 2008, 16: 1291-1298. 10.1007/s00520-008-0425-1.
Costa D, Mogos I, Toma T: Efficacy of mianserin in the treatment of depression of women with cancer. Acta Psychiatrica Scandinavia. 1985, 72 (suppl. 320): 85-92.
Van Heeringen K, Zivkov M: Pharmacological treatment of depression in cancer patients. A placebo controlled study of mianserine. Br J Psychiatry. 1996, 169: 440-443. 10.1192/bjp.169.4.440.
Razavi D, Allilaire JF, Smith M, Salimpour A, Verra M, Desclaux B, Saltel P, Piollet I, Gauvain-Piquard A, Trichard C, Cordier B, Fresco R, Guillibert E, Sechter D, Orth JP, Bouhassira M, Mesters P, Blin P: The effect of fluoxetine on anxiety and depression symptoms in cancer patients. Acta Psychiatrica Scandinavia. 1996, 94: 205-210. 10.1111/j.1600-0447.1996.tb09850.x.
Fisch MJ, Loehrer PJ, Kristeller J, Passik S, Jung SH, Shen SH, Arquette MA, Brames MJ, Einhorn LH: Fluoxetine versus Placebo in advanced cancer outpatients: a double-blinded trial of the Hoosier oncology group. J Clin Oncol. 2003, 21: 1937-1943. 10.1200/JCO.2003.08.025.
Navari RM, Brenner MC, Wilson MN: Treatment of depressive symptoms in patients with early stage breast cancer undergoing adjuvant therapy. Breast Cancer Res Treat. 2008, 112: 197-201. 10.1007/s10549-007-9841-z.
Musselmann DL, Somerset WI, Guo Y, Manatunga AK, Porter M, Penna S, Lewison B, Goodkin R, Lawson K, Lawson D, Evans DL, Nemeroff CB: A double-blind multicenter parallel-group study of paroxetine, desipramine or placebo in breast cancer patients (stages I, II, III, IV) with major depression. J Clin Psychiatry. 2006, 67: 288-296. 10.4088/JCP.v67n0217.
Morrow GR, Hickok JT, Roscoe JA, Raubertas RF, Andrews PLR, Flynn PJ, Hynes HE, Banerjee TK, Kirschner JJ, King DK: Differential effects of paroxetine on fatigue and depression: a randomized, double blind trial from the University of Rochester Cancer Center Community Clinical Oncology Program. J Clin Oncol. 2003, 21: 4635-4641. 10.1200/JCO.2003.04.070.
Roscoe JA, Morrow GR, Hickok JT, Mustian KM, Griggs JJ, Matteson SE, Bushunow P, Qazo R, Smith B: Effect of paroxetine hydrochloride on fatigue and depression in breast cancer patients receiving chemotherapy. Breast Cancer Res Treat. 2005, 89: 243-249. 10.1007/s10549-004-2175-1.
Stockler MR, O´Connel R, Nowak AK, Goldstein D, Turner J, Wilcken NRC, Wyld D, Abdi EA, Glasgow A, Beale PJ, Jefford M, Dhillon H, Heritier S, Carter C, Hickie IB, Simes RJ: Effect of sertraline on symptoms and survival in patients with advanced cancer, but without major depression: a placebo controlled double-blind randomized trial. Lancet Oncol. 2007, 8: 603-612. 10.1016/S1470-2045(07)70148-1.
Musselmann DL, Lawson DH, Gumnick JF, Manatunga AK, Penna S, Goodkin RS, Greiner K, Nemeroff CB, Miller AH: Paroxetine for the prevention of depression induced by high dose interferone alpha. N Engl J Med. 2001, 344: 961-966. 10.1056/NEJM200103293441303.
Lydiatt WM, Denman D, McNeilly DP, Puumula SE, Burke WJ: A randomized placebo- controlled trial of citalopram for the prevention of major depression during treatment for head and neck cancer. Arch Otolaryngol Head Neck Surg. 2008, 134: 528-535. 10.1001/archotol.134.5.528.
Massie MJ, Gagnon P, Holland GC: Depression and suicide in patients with cancer. J Pain Symptom Manage. 1994, 9: 325-340. 10.1016/0885-3924(94)90192-9.
Van der Feltz-Cornelis CM, Nuyen J, Stoop C, Chan J, Jacobson AM, Katon W, Snoek F, Sartorius N: Effect of interventions for major depressive disorder and significant depressive symptoms in patients with diabetes mellitus: a systematic review and meta-analysis. Gen Hosp Psychiatry. 2010, 32: 380-395. 10.1016/j.genhosppsych.2010.03.011.
Price A, Rayner L, Okon-Rocha E, Evans A, Valsraj K, Higginson IJ, Hotopf M: Antidepressants for the treatment of depression in neurological disorders: a systematic review and meta-analysis of randomized controlled trials. J Neurol Neurosurg Psychiatry. 2011, 82: 914-923. 10.1136/jnnp.2010.230862.
Sherwood Brown E, Vigil L, Khan DA, Liggin JDM, Carmody TJ, John Rush A: A randomized controlled trial of citalopram versus placebo on outpatients with asthma and major depressive disorder: a proof of concept study. Biol Psychiatry. 2005, 58: 865-870. 10.1016/j.biopsych.2005.04.030.
Baumeister H, Hutter N, Bengel J: Psychological and pharmacological interventions for depression in patients with coronaryartery disease. Cochrane Database Syst Rev. 2011, Art.No.:CD008012-http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD008012.pub3/pdf, Issue 9,
Baumeister H, Hutter N, Bengel J: Psychological and pharmacological interventions for depression in patients with coronary artery disease. The Cochrane Collaboration. 2011
Graff LA, Walker JR, Bernstein CN: Depression and anxiety in inflammatory bowel disease: a review of comorbidity and management. Inflammatory Bowel Disease. 2009, 15: 1105-1118. 10.1002/ibd.20873.
Clink HM: Mianserin and blood dyscrasias. Br J Clin Pharmacol. 1983, 15 (Suppl. 2): 291-293.
Henry NL, Rae JM, Li L, Azzouz F, Skaar TC, Desta Z, Sikora MJ, Philips S, Nguyen AT, Storniolo AM, Hayes DF, Flockhart DA: Stearns V; Consortium on Breast Cancer Pharmacogenomics Investigators: Association between CYP2D6 genotype and tamoxifen-induced hot flashes in a prospective cohort. Breast Cancer Res Treat. 2009, 117: 571-575. 10.1007/s10549-009-0309-1.
Desmarais JE, Looper KJ: Interactions between tamoxifen and antidepressants via cytochrome P450 2D6. J Clin Psychiatry. 2009, 70: 1688-1697. 10.4088/JCP.08r04856blu.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-244X/13/140/prepub
The study was supported by the German Research Foundation (DFG; MA2631/4-1). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We would like to thank Martina Haeck MD for the helpful discussions.
The authors declare that they have no competing interests.
Zacharias G. Laoutidis participated in data collection and evaluation, performed the statistical analysis and drafted the manuscript. Klaus Mathiak conceived and designed the study, acquired the funding, participated in and supervised collection of data, and helped to draft the manuscript. Both authors read and approved the manuscript.
About this article
Cite this article
Laoutidis, Z.G., Mathiak, K. Antidepressants in the treatment of depression/depressive symptoms in cancer patients: a systematic review and meta-analysis. BMC Psychiatry 13, 140 (2013). https://doi.org/10.1186/1471-244X-13-140
- Depressive symptoms