Department of Forensic Psychiatry, Niuvanniemi Hospital, University of Eastern Finland, Kuopio, Finland; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden; Center for Psychiatry Research, Stockholm City Council, Stockholm, Sweden; Neuroscience Center, University of Helsinki, Helsinki, Finland.
Department of Forensic Psychiatry, Niuvanniemi Hospital, University of Eastern Finland, Kuopio, Finland; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden; Center for Psychiatry Research, Stockholm City Council, Stockholm, Sweden.
Lancet Psychiatry. 2022 May;9(5):353-362. doi: 10.1016/S2215-0366(22)00044-X. Epub 2022 Mar 22.
Clozapine is the most efficacious treatment for schizophrenia and is associated with lower overall mortality than are other antipsychotic drugs, despite the risk of agranulocytosis. Preliminary reports over the past 10 years suggest a possible risk of haematological malignancies, but the issue has remained unsettled. We aimed to study the risk of haematological malignancies associated with use of clozapine and other antipsychotics.
We did a nationwide case-control (and cohort) study of people with schizophrenia, using prospectively gathered data from Finnish national registers. A nested case-control study was constructed by individually matching cases of lymphoid and haematopoietic tissue malignancy with up to ten controls without cancer by age, sex, and time since first schizophrenia diagnosis. For the case-control study, we restricted inclusion criteria to malignancies diagnosed on a histological basis, and excluded individuals outside of the age range 18-85 years, and any patients that had a previous malignancy. Analyses were done using conditional logistic regression adjusting for comorbid conditions.
For the case-control study 516 patients with a first-time diagnosis of lymphoid and haematopoietic tissue malignancy during years 2000-17 and diagnosed after their first diagnosis of schizophrenia were identified. 102 patients were excluded due to diagnosis that was without a histological basis, five patients were excluded because of their age, and 34 were excluded for a previous malignancy, resulting in 375 patients being matched to controls. We selected up to ten controls without cancer (3734 in total) for each case from the base cohort of people with schizophrenia. For the cohort study, data for 55 949 people were included for analysis. Cumulative incidence of haematological malignancies during the mean follow-up of 12·3 years (SD 6·5) was 102 (0·7%) cases among 13 712 patients who had used clozapine (corresponding to event rate of 61 cases per 100 000 person-years), and during mean follow-up of 12·9 years (SD 7·2) was 235 (0·5%) malignancies among 44 171 patients having used other antipsychotic medication than clozapine (corresponding to 41 cases per 100 000 person-years). Of the 375 individuals with haematological malignancies (305 lymphomas, 42 leukaemia, 22 myelomas, 6 unspecified) observed from 2000-17, 208 (55%) were males and 167 (45%) were female. Ethnicity data were not available. Compared with non-use of clozapine (most had used other antipsychotics and a few had used no antipsychotics), clozapine use was associated with increased odds of haematological malignancies in a dose-response manner (adjusted odds ratio 3·35, [95% CI 2·22-5·05] for ≥5000 defined daily dose cumulative exposure, p<0·0001). Exposure to other antipsychotic drugs was not associated with increased odds. A complementary analysis showed that the clozapine-related risk increase was specific for haematological malignancies, because no such finding was observed for other malignancies. Over 17 years of follow-up of the base cohort, 37 deaths occurred due to haematological malignancy among patients exposed to clozapine (26 with ongoing use at time of haematological malignancy diagnosis, and 11 in patients who did not use clozapine at the exact time of their cancer diagnosis), whereas only three deaths occurred due to agranulocytosis.
Unlike other antipsychotics, long-term clozapine use is associated with increased odds of haematological malignancies. Long-term clozapine use has a higher effect on mortality due to lymphoma and leukaemia than due to agranulocytosis. However, acknowledging that the absolute risk is small compared with the previously observed absolute risk reduction in all-cause mortality is important. Our results suggest that patients and caregivers should be informed about warning signs of haematological malignancies, and mental health clinicians should be vigilant for signs and symptoms of haematological malignancy in patients treated with clozapine.
The Finnish Ministry of Social Affairs and Health and Academy of Finland.
氯氮平是治疗精神分裂症最有效的药物,与其他抗精神病药物相比,其总体死亡率较低,尽管其会引起粒细胞缺乏症。过去 10 年的初步报告表明,氯氮平可能存在血液恶性肿瘤的风险,但该问题仍未得到解决。我们旨在研究使用氯氮平和其他抗精神病药物与血液恶性肿瘤风险的关系。
我们使用来自芬兰国家登记处的前瞻性收集的数据,对精神分裂症患者进行了全国性病例对照(和队列)研究。通过对每个病例与年龄、性别和首次诊断为精神分裂症后的时间相匹配的至多 10 名无癌症的对照进行嵌套病例对照研究,构建了一个病例对照研究。对于病例对照研究,我们将纳入标准仅限于基于组织学诊断的恶性肿瘤,并排除年龄在 18-85 岁以外的患者和任何有既往恶性肿瘤的患者。分析使用条件逻辑回归进行,调整了合并症的情况。
在病例对照研究中,我们确定了 2000-17 年期间首次诊断为血液和淋巴组织恶性肿瘤的 516 名患者,这些患者在首次诊断为精神分裂症后被诊断出患有该疾病。由于诊断缺乏组织学基础,102 名患者被排除在外,5 名患者因年龄被排除在外,34 名患者因既往恶性肿瘤被排除在外,最终有 375 名患者与对照组相匹配。我们从精神分裂症患者的基础队列中为每个病例选择了至多 10 名无癌症的对照(总共 3734 名)。对于队列研究,我们纳入了 55949 名患者的数据进行分析。在平均随访 12.3 年(标准差 6.5)期间,使用氯氮平的 13712 名患者中有 102 例(0.7%)发生血液恶性肿瘤(相应的事件发生率为每 100000 人年 61 例),在平均随访 12.9 年(标准差 7.2)期间,使用氯氮平以外的其他抗精神病药物的 44171 名患者中有 235 例(0.5%)发生血液恶性肿瘤(相应的事件发生率为每 100000 人年 41 例)。在 2000-17 年间观察到的 375 例血液恶性肿瘤患者(305 例淋巴瘤、42 例白血病、22 例骨髓瘤、6 例未明确)中,208 例(55%)为男性,167 例(45%)为女性。种族数据不可用。与未使用氯氮平(大多数使用了其他抗精神病药物,少数未使用任何抗精神病药物)相比,氯氮平的使用与血液恶性肿瘤的发生风险呈剂量反应关系(调整后的比值比 3.35,[95%CI 2.22-5.05],累积暴露≥5000 定义日剂量,p<0.0001)。使用其他抗精神病药物与发生风险增加无关。一项补充分析表明,氯氮平相关的风险增加是针对血液恶性肿瘤的,因为在其他恶性肿瘤中没有发现这种现象。在基础队列的 17 年随访期间,在暴露于氯氮平的患者中,有 37 例因血液恶性肿瘤而死亡(26 例在血液恶性肿瘤诊断时仍在使用氯氮平,11 例在癌症诊断时未使用氯氮平),而仅有 3 例死于粒细胞缺乏症。
与其他抗精神病药物不同,长期使用氯氮平与血液恶性肿瘤的发生风险增加相关。与粒细胞缺乏症相比,长期使用氯氮平对淋巴瘤和白血病相关的死亡率影响更大。然而,重要的是要认识到与先前观察到的全因死亡率绝对降低相比,这种绝对风险仍然较小。我们的研究结果表明,应告知患者和护理人员血液恶性肿瘤的警告信号,精神卫生临床医生应警惕使用氯氮平治疗的患者出现血液恶性肿瘤的症状和体征。
芬兰社会事务和卫生部以及芬兰科学院。