新引入olaparib的患者中贫血的发展因素:一个回顾性病例控制研究
Chihiro Shiraishi1, Toshinori Hirai1, Michiko Kaneda2
1Department of Pharmacy, Mie University Hospital, Mie, Japan.
Medicine
|July 28, 2023
概括
奥拉巴里布经常导致贫血,通常是宏细胞性,即使没有叶酸或维生素B12缺乏. 在接受olaparib的患者中,先前高剂量的卡博普拉丁和失血症可能会增加贫血风险.
科学领域:
- 在瘤学瘤学.
- 血液学 血液学 血液学
- 药理学 药理学是指药理学的学科.
背景情况:
- 贫血是olaparib的常见剂量限制性毒性.
- 关于olaparib诱导的贫血的临床特征的数据有限.
- 营养因素,如叶酸和维生素B12在这种毒性中的作用还不清楚.
研究的目的:
- 为了研究olaparib诱导的贫血的临床特征.
- 为了检查叶酸或维生素B12在olaparib引起的贫血中的潜在作用.
- 为了探索olaparib诱导的贫血和之前的碳波拉丁暴露或胃肠道事件之间的关联.
主要方法:
- 对接受olaparib.com的患者进行了回顾性病例控制研究.
- 在olaparib治疗期间发生≥3级贫血的患者的分析.
- 在接受卵巢或子宫内膜癌治疗的患者中评估叶酸和维生素B12水平的子研究.
主要成果:
- 45%的患者患有≥3级贫血,往往需要降低剂量或停止治疗.
- 50%的患有严重贫血的患者表现出宏细胞贫血,经常发生在那些先前接触过碳波拉丁的患者中.
- 在患有贫血的患者中,没有发现叶酸或维生素B12缺乏;然而,失血症更为常见.
结论:
- 奥拉巴里布诱导的贫血通常呈现为宏细胞或常细胞红细胞贫血.
- 贫血是独立于叶酸或维生素B12缺乏而发生的.
- 高累积剂量之前的卡博普拉丁和dysgeusia可能与olaparib诱导的贫血有关.
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