BRAF and MEK inhibitors rechallenge after an adverse drug reaction in patients with cancer: A pharmacovigilance cohort study.

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Emilien Ezine, Angélique Da Silva, Safa Idoudi, Céleste Lebbe, Basile Chrétien, Marion Sassier, Joachim Alexandre, Charles Dolladille
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引用次数: 0

Abstract

Importance: The safety profile of a rechallenge with BRAF inhibitors (BRAFi) or a combination of BRAF and MEK inhibitors (MEKi) following an adverse drug reaction (ADR) remains largely unexplored.

Objective: To identify the reported recurrence rate of the same ADR after a BRAFi±MEKi targeted therapy (TT) rechallenge in patients with cancer and to identify factors associated with recurrence.

Design, setting, and participants: In this observational, pharmacovigilance study, ADR reports were sourced from VigiBase, the World Health Organization database. The inclusion criteria encompassed all BRAFi cases (with or without MEKi) through September 01, 2023, irrespective of the primary cancer diagnosis.

Main outcomes and measures: The primary outcome was the reported recurrence rate of the same initial ADR following TT rechallenge. Secondary outcomes measures included were identification of variables associated with recurrence among informative rechallenges, defined as those with known recurrence status.

Results: Out of 21,339 ADR cases linked to TT, 4771 (22.4%) reported a rechallenge, with 563 yielding informative data (11.8%). Recurrence of the initial ADR was reported in 223 cases, resulting in a reported recurrence rate of 39.6% (95% CI: 35.7-43.7). The highest recurrence rates in a rechallenge were observed for pyrexia (47%, 95% CI: 39-55), renal failure (46%, 95% CI: 32-60), and musculoskeletal disorders (44%, 95%CI: 33-56). There was no significant influence of factors such as TT regimen (either BRAFi monotherapy or any TT combination), age, sex, or the type of cancer on reported recurrence rate.

Conclusions and relevance: In real-world settings, approximately two-fifths of cases with notified TT rechallenges led to a reporting of recurrence of the same initial ADR. The primary determinant of reported recurrence seems to be the nature of the initial ADR rather than the TT regimen, or any other baseline patient characteristic.

BRAF和MEK抑制剂在癌症患者发生药物不良反应后再次挑战:一项药物警戒队列研究
重要性:BRAF抑制剂(BRAFi)或BRAF和MEK抑制剂联合(MEKi)在药物不良反应(ADR)后再次挑战的安全性仍未得到充分研究。目的:了解肿瘤患者BRAFi±MEKi靶向治疗(TT)再挑战后相同不良反应的复发率及复发相关因素。设计、环境和参与者:在这项观察性药物警戒研究中,不良反应报告来自世界卫生组织数据库VigiBase。纳入标准包括截至2023年9月1日的所有BRAFi病例(伴或不伴MEKi),无论原发癌症诊断如何。主要结果和指标:主要结果是TT再挑战后相同初始不良反应的报告复发率。次要结果测量包括在信息性再挑战中识别与复发相关的变量,定义为已知复发状态的变量。结果:在21339例与TT相关的ADR病例中,4771例(22.4%)报告了再次挑战,其中563例(11.8%)提供了信息数据。223例报告了初始不良反应的复发,导致报告的复发率为39.6% (95% CI: 35.7-43.7)。再挑战中复发率最高的是发热(47%,95%CI: 39-55)、肾功能衰竭(46%,95%CI: 32-60)和肌肉骨骼疾病(44%,95%CI: 33-56)。TT方案(BRAFi单药治疗或任何TT联合治疗)、年龄、性别或癌症类型等因素对报告的复发率没有显著影响。结论和相关性:在现实环境中,大约五分之二的通报TT再挑战病例导致报告相同的初始ADR复发。报告复发的主要决定因素似乎是初始不良反应的性质,而不是TT治疗方案或任何其他基线患者特征。
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来源期刊
Therapie
Therapie 医学-药学
CiteScore
3.50
自引率
7.70%
发文量
132
审稿时长
57 days
期刊介绍: Thérapie is a peer-reviewed journal devoted to Clinical Pharmacology, Therapeutics, Pharmacokinetics, Pharmacovigilance, Addictovigilance, Social Pharmacology, Pharmacoepidemiology, Pharmacoeconomics and Evidence-Based-Medicine. Thérapie publishes in French or in English original articles, general reviews, letters to the editor reporting original findings, correspondence relating to articles or letters published in the Journal, short articles, editorials on up-to-date topics, Pharmacovigilance or Addictovigilance reports that follow the French "guidelines" concerning good practice in pharmacovigilance publications. The journal also publishes thematic issues on topical subject. The journal is indexed in the main international data bases and notably in: Biosis Previews/Biological Abstracts, Embase/Excerpta Medica, Medline/Index Medicus, Science Citation Index.
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