Rare but elevated incidence of hematological malignancy after clozapine use in schizophrenia: A population cohort study.

Publication date: Dec 01, 2024

Clozapine is widely regarded as a highly efficacious psychotropic drug that is largely underused worldwide. Recent disproportionality analyses and nationwide case-control studies suggested a potential association between clozapine use and hematological malignancy (HM). Nevertheless, the absolute rate difference is not well-established due to the absence of analytic cohort studies. The clinical significance of such a potential risk remains unclear. We extracted data from a territory-wide public healthcare database from January 2001 to August 2022 in Hong Kong to conduct a retrospective cohort study of anonymized patients aged 18+ years with a diagnosis of schizophrenia who used clozapine or olanzapine (drug comparator with highly similar chemical structure and pharmacological mechanisms) for 90+ days, with at least 2 prior other antipsychotic use records within both groups. Weighted by inverse probability of treatment (IPTW) based on propensity scores, Poisson regression was used to estimate the incidence rate ratio (IRR) of HM between clozapine and olanzapine users. The absolute rate difference was also estimated. In total, 9,965 patients with a median follow-up period of 6. 99 years (25th to 75th percentile: 4. 45 to 10. 32 years) were included, among which 834 were clozapine users. After IPTW, the demographic and clinical characteristics of clozapine users were comparable to those of olanzapine users. Clozapine users had a significant weighted IRR of 2. 22 (95% confidence interval (CI) [1. 52, 3. 34]; p < 0. 001) for HM compared to olanzapine users. The absolute rate difference was estimated at 57. 40 (95% CI [33. 24, 81. 55]) per 100,000 person-years. Findings were consistent across subgroups by age and sex. Sensitivity analyses all supported the robustness of the results and showed good specificity to HM but no other cancers. The main limitation of this observational study is the potential residual confounding effects that could have arisen from the lack of randomization in clozapine or olanzapine use. Absolute rate difference in HM incidence associated with clozapine is small despite a 2-fold elevated rate. Given the rarity of HM and existing blood monitoring requirements, more restrictive indication for clozapine or special warnings may not be necessary.

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Concepts Keywords
August Adolescent
Healthcare Adult
Schizophrenia Aged
Antipsychotic Agents
Antipsychotic Agents
Clozapine
Clozapine
Cohort Studies
Female
Hematologic Neoplasms
Hong Kong
Humans
Incidence
Male
Middle Aged
Olanzapine
Olanzapine
Retrospective Studies
Schizophrenia
Young Adult

Semantics

Type Source Name
disease MESH hematological malignancy
drug DRUGBANK Clozapine
disease MESH schizophrenia
disease MESH clinical significance
drug DRUGBANK Olanzapine
disease MESH cancers
disease IDO blood
disease MESH Suicide
disease IDO history
disease IDO process
pathway REACTOME Reproduction
drug DRUGBANK Medical air
disease MESH COVID 19
disease MESH abnormalities
disease MESH agranulocytosis
disease MESH eosinophilia
disease MESH cytopenia
disease MESH treatment resistant schizophrenia
drug DRUGBANK Aspartame
drug DRUGBANK Ilex paraguariensis leaf
disease MESH tic
disease MESH death
drug DRUGBANK Isoxaflutole
drug DRUGBANK Indole
disease MESH mental disorder
disease MESH depression
disease MESH dementia
disease MESH asthma
pathway KEGG Asthma
drug DRUGBANK Coenzyme M
drug DRUGBANK L-Phenylalanine
disease MESH immunological diseases
disease MESH Bipolar disorder
disease MESH Autoimmune Diseases
disease MESH Vitiligo
disease MESH Addison disease
disease MESH Alopecia areata
disease MESH thyroiditis
disease MESH Graves’ disease
disease MESH Multiple sclerosis
disease MESH Myasthenia gravis
disease MESH Pernicious anemia
disease MESH Primary biliary cirrhosis
disease MESH Takayasu arteritis
disease MESH diabetes mellitus
disease MESH Episcleritis
disease MESH Erythema nodosum
disease MESH anemia
disease MESH Immune thrombocytopenia
disease MESH purpura
disease MESH Leukocytoclastic vasculitis
disease MESH Myositis
disease MESH Pulmonary fibrosis
disease MESH interstitial lung disease
disease MESH syndrome
disease MESH Sjogren’s syndrome
disease MESH Thrombocytopenia
disease MESH Vasculitis
disease MESH juvenile idiopathic arthritis

Original Article

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