Evaluation of patients on sertindole treatment after failure of other antipsychotics: A retrospective analysis
© Azorin et al; licensee BioMed Central Ltd. 2008
Received: 11 May 2007
Accepted: 14 March 2008
Published: 14 March 2008
Use of the atypical antipsychotic sertindole was suspended for four years due to safety concerns. During the suspension, the regulatory authorities required further studies, including this one, to be conducted. The purpose of this study was to determine if a subset of patients with psychotic illness exists which particularly benefits from sertindole treatment after failure of other antipsychotic drugs, including atypical antipsychotics.
This was a retrospective single-arm observational crossover study of 344 patients, who served as their own controls. Patients mainly from the Sertindole Safety Study who had shown good response to sertindole, and who had followed up to four alternating six month periods of treatment with sertindole and other antipsychotics, were included. (In Period 1 patients took non-sertindole treatment, in Period 2, sertindole was taken, in Period 3, patients reverted to non-sertindole treatment, and in Period 4, sertindole was taken again.) Patient records for each period of treatment were assessed for objective data: number and duration of hospitalizations due to worsening of psychotic symptoms; the amount of self-harming behaviour; indicators of social status. Retrospective evaluation of changes in clinical symptoms from the patients' records was also conducted. Dates and reasons for stopping and/or switching medication were also recorded.
There was improvement in all objective measured parameters during the periods of sertindole treatment. In particular, the average number of hospitalizations per year due to worsening of psychotic symptoms was reduced in the following way in the group studied over four treatment periods: Period 1 (non-sertindole treatment) 3.4; Period 2 (sertindole treatment) 1.0; Period 3 (non-sertindole treatment) 2.0; Period 4 (sertindole treatment) 1.8. The duration of hospitalizations also decreased significantly during the periods of sertindole treatment. Results showed that patients improved in objective social parameters when switched to sertindole treatment; assessment of the patients' affective lives showed a significant increase in the number of patients having a stable relationship during sertindole treatment; and assessment of the number of patients employed showed an increase after the first and second switch to sertindole treatment (from Period 1 to Period 2 and from Period 3 to Period 4, respectively).
Adverse events and lack of efficacy were the main reasons for switching to sertindole.
A group of patients benefited from sertindole after other antipsychotic treatments, including that with atypical antipsychotics, had failed. Further studies are needed to investigate if there is a specific patient profile that corresponds to these responders.
Schizophrenia is a chronic, complex, and heterogeneous disease that affects most aspects of psychological functioning. The disease is frequently associated with cognitive and depressive symptoms and commonly manifests at an early adult age. It can have a devastating impact on familial, social and vocational aspects of patients' lives [1–3]. Long-term treatment with antipsychotic drugs is the major factor in preventing relapse [4–6].
For the patient suffering from schizophrenia it is crucially important to receive the best possible treatment. The individual responses to different treatments are highly variable, and therefore a wide selection of clinically efficacious and safe drugs will maximize the chances that the appropriate treatment is eventually prescribed to each patient [7, 8].
Although clozapine has been a great improvement in addressing unmet medical needs for treatment-resistant patients, it is still thought that many patients with schizophrenia do not respond to any available antipsychotic treatment [9, 10].
Sertindole is an atypical antipsychotic drug indicated for the treatment of schizophrenia. It was first authorised in the United Kingdom in 1996 and subsequently in other European countries. Due to concerns related to cardiac safety which arose after its launch, the marketing of sertindole was suspended by Lundbeck in November 1998 .
In June 1999, the European Committee for Proprietary Medicinal Products (CPMP, now the CHMP) adopted an Opinion recommending the temporary suspension of the Marketing Authorizations for sertindole and asked for a complementary benefit/risk evaluation of the product . The present study (the "NICHE" study) was part of this evaluation. It was performed in order to respond to the question of whether there is a subset of patients that clearly improve during sertindole treatment after failure with other antipsychotics.
This observational study was designed in order to include patients who had two non-consecutive treatment periods with sertindole. Since market availability of sertindole was restricted after the suspension, patients were mainly selected from those who were identified in a previous survey, the Sertindole Safety Survey  therefore giving the name the present study, the NICHE study.
The NICHE study provided an opportunity to document the improvement, or otherwise, of a subset of patients who had benefited from sertindole treatment, and for whom alternative therapies had not shown comparable results. The assessment of safety was not an objective of this study, as this was addressed in the Sertindole Safety study.
Total number of patients per country
Number of patients n (%)
In order to include patients who had two non-consecutive treatment periods with sertindole, patients were selected from those who had been treated through the named-patient program (set up after sertindole suspension), and who were identified in a previous survey, the Sertindole Safety Survey.
The Sertindole Niche Survey is a retrospective study, with no patient exclusion criteria and no personal identification required. For this study there was no need for ethics committee approval of the study according to the countries regulations at the time of conduction of this study in Austria, Belgium, Czech Republic, Estonia, Finland, France, Germany, Hungary, Latvia, Netherlands and United Kingdom.
The Sertindole Niche Survey was based on the Sertindole Safety Survey, for which local regulatory rules were followed in each participating country. Where applicable, the Sertindole Safety Survey study was submitted to and approved by the relevant authorities and/or local ethics committee/institutional review board.
Patients were 18 years or older; their primary diagnosis was that of a psychosis, mainly schizophrenia.
The age, gender, DSM IV classification, history of psychiatric disorder, general medical history, and history of drug abuse of the patients were recorded before the evaluation.
All antipsychotic medication taken within the observational period was recorded, including the type of drug, the indication, the dose, the start and end date of treatment, and the reason for stopping or switching medication. Concomitant medication was not recorded.
This was a single-arm, retrospective, crossover study. Data collection was not blinded and treatments had not been randomly allocated. The patient served as his or her own control.
All patients followed alternate periods of antipsychotic treatments: after an initial treatment period on a non-sertindole antipsychotic regimen of at least six months, patients who either were not responding or were experiencing tolerability problems, were switched to sertindole treatment (Figure 1). Following sertindole's market suspension, patients were switched again to other antipsychotics. Subsequently, some of the patients went on to receive a further period of sertindole treatment, under the named patient compassionate use programme. Up to four treatment periods of around six months each were thus studied. This design thus produced three separate patient groups from the initial 344 patients: a group of patients that had experienced only two treatment periods, a group of patients that had experienced three treatment periods, and a group of patients that had experienced four treatment periods.
For each treatment period, patient records were assessed for objective parameters (the number of hospitalizations and the amount of self-aggression behaviour [self-harm and suicide attempts]). These data are supportive of the retrospective data on patient clinical symptoms (measured by the Clinical Global Impression and Global Assessment Function scales).
The psychiatrist attending each patient retrospectively assessed the longitudinal course of the psychosis using the five main symptoms defined in the DSM IV for psychosis longer than one year (all types considered). These symptoms were rated from 0 to 3 according to intensity (0 = absent, 3 = severe). In addition, the following assessments and records were used to support the data:
Clinical symptom evaluation was based on the Clinical Global Impression (CGI) and the Global Assessment Function (GAF) scales.
The number of hospitalizations and the number of days in hospital were recorded.
Self-harming behaviour was assessed by the number of suicide and self-harm attempts made.
The presence of a stable personal relationship and the employment status provided objective information in support of the social assessments.
The statistics were essentially descriptive. The results were analysed taking into account the score of each individual item, enabling the comparison of the results between different periods.
Number of hospitalizations, duration of hospitalization, and number of self-harm and suicide attempts were computed by treatment period. Data were analysed using SAS software (version 6.12). Quantitative variables were expressed as mean ± standard deviation (SD), while qualitative variables were presented using frequencies and percentages. Chi-square tests (or Fisher's exact tests when appropriate), as well as t-tests (or Mann-Whitney tests when appropriate) were used to compare qualitative or quantitative data. All statistical tests were two-sided, with the α risk set to 0.05.
Patients' profiles at start of study
Patient clinical profile at baseline
Patients' baseline profile
Number of patients n (%)
Other than schizophrenia
Concomitant mental disorders
Anxiety and other disorders
Hospitalization due to psychosis
Last hospitalization duration > 1 month
Patients that had been physically violent towards another person at least once
Patients that had attempted self-harm at least once
Patients' profiles during the treatment periods
Comparison of duration of treatment periods
Mean duration ± SD (months)
8.7 ± 5.9
7.1 ± 5.2
6.4 ± 4.3
Antipsychotic treatment during Period 1 and Period 3
Type of Antipsychotic
Period 1 n (%)
Period 3 n (%)
Four treatment period group (P1–P4)
Only typical antipsychotics
At least one atypical antipsychotic
Three treatment period group (P1–P3)
Only typical antipsychotics
At least one atypical antipsychotic
Two treatment period group (P1–P2)
Only typical antipsychotics
At least one atypical antipsychotic
The main reasons for switching to sertindole at the end of the first treatment period (P1) were found to be firstly, lack of efficacy, and secondly, experience of adverse events under the previous treatment.
The main reason for stopping sertindole after Period 2 was due to its market suspension or consequent difficulties in supply.
Results from the group that followed four treatment periods (P1–P4)
The number of self-harm and suicide attempts was significantly reduced during both sertindole periods compared to the non-sertindole periods. After starting the first sertindole treatment the percentage of self-harm attempts decreased from 22.8% to 3.5% (p < 0.001), and during the second period of sertindole treatment it reduced from 5.8% to 1.8% (p < 0.05). The number of suicide attempts also followed this trend with a reduction from 15.8% to 3.5%, and from 7.0% to 0%, during the first and second sertindole-treatment periods, respectively.
Objective Social Assessments
Patients' Affective Lives Engaged in a stable relationship
Employment and Occupational Status Employed most of the time
Remission profile in the four treatment period group
Type of course
Period 1 n (%)
Period 2 n (%)
Period 3 n (%)
Period 4 n (%)
Single episode in full remission
The results show that there is a subset of patients who were switched to sertindole that had an improvement in their clinical symptoms, which was reflected in a decrease in the number and duration of hospitalizations, as well as suicide attempts.
When sertindole was first suspended from the market, it could only be prescribed under the named-patient program. Although some clinicians continued to prescribe sertindole, many patients were switched to other treatments. From clinical observation, it was suggested that there might be a subset of patients who respond uniquely to sertindole . In order to identify whether this proposed subset of patients exists, we conducted this retrospective study of the health records of patients who had received alternate periods of non-sertindole antipsychotic drug therapy and sertindole therapy. This study was conducted using retrospective methodology, as sertindole was suspended at the time and it was not possible to run prospective clinical trials.
This study was not designed to compare antipsychotics, but to document, in a standardised way, if a subset of patients exists for whom multiple previous antipsychotic treatments had not been satisfactory, but who had improved with sertindole. As a result, the total number of patients to be included was not calculated. Because the study was conducted retrospectively, the treatment pattern and patient management were unaffected by the conduct of the study. However, the treatments were not randomly allocated and the reliability of the unblinded efficacy data may be questioned. Data collection was therefore standardised for the various assessment periods, using both objective criteria (number and duration of hospitalizations, number self-harm and suicide attempts, patient's affective life and employment and occupational status) and subjective criteria (the clinical scorings, GAF, CGI).
Each patient served as his or her own control, and comparisons were achieved in crossover periods in the patients who followed four treatment periods. The results from the group of patients who followed the four treatment periods provide the strongest possible indicator for the causal relationship between sertindole treatment and improvement in symptoms. This design could be compared to the challenge-dechallenge-rechallenge strategy in pharmacovigilance.
Results from the patients who followed only two or three alternate treatment periods, although confirming what was observed in the P1–P4 group, have not been reported here in detail, as they were not the focus of this article. It would be interesting to analyse the results between these groups in further studies. The individual clinical results have not been analysed statistically as the patients were not randomly selected (only patients who responded to sertindole treatment were included), and analysis would have had no value.
The improvements in all criteria during the sertindole treatment periods provide evidence of a sub-group of patients who respond particularly well to this drug. In particular, the reduction in number of hospitalizations due to worsening of psychotic symptoms provides objective evidence for this improvement, as hospitalization for worsening of psychosis has been demonstrated to be a good indicator of relapse in patients with schizophrenia .
Why a particular subgroup of patients responds to sertindole in this way is unknown, but it may be related to the specific chemical structure and the specific receptor profile which lead to the unique pharmacological profile of the drug . This is characterised by selective inhibition of dopaminergic activity in the mesolimbic pathway, with very little inhibition of the nigrostriatal dopaminergic neurons [16, 17]. This affinity profile provides antipsychotic effectiveness without the level of extrapyramidal symptoms seen with conventional agents .
The present study methodology does not enable us to estimate how many patients within the overall population suffering from schizophrenia would respond in a similarly effective way to sertindole. In addition, the study does not permit us to establish a profile of the patients who may respond particularly well to sertindole, as our sample was small and not representative of the overall population suffering from schizophrenia. It would be interesting for further studies to investigate if these patients who respond particularly well to sertindole have specific clinical characteristics, thus enabling targeted prescription.
Patients included in this study showed a significant improvement of psychotic symptoms when treated with sertindole after failure of another antipsychotic. This study results have therefore been used for the response to the authorities, as providing evidence that there is indeed a subset of patients who benefit from sertindole after other antipsychotics, including clozapine, have failed.
The authors gratefully acknowledge the comments and suggestions by Christophe Sapin concerning the statistics, as well as the editorial assistance of Catriona Holmes in the preparation of this manuscript.
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