Department of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seongnam, Republic of Korea.
Department of Obstetrics and Gynecology, CHA Gangnam Medical Center, CHA University School of Medicine, 566 Nonhyeon-ro, Gangnam-gu, Seoul, 06135, Republic of Korea.
Arch Gynecol Obstet. 2022 Aug;306(2):443-449. doi: 10.1007/s00404-022-06403-9. Epub 2022 Jan 19.
We aimed to identify the predictive risk factors for carboplatin-related hypersensitive reactions (HRs) and investigate their impact on survival outcomes in patients with epithelial ovarian cancer (EOC).
This retrospective study included 222 patients with EOC who received carboplatin infusion between July 2016 and November 2019. We compared the clinicopathologic characteristics and survival outcomes between carboplatin-related hypersensitivity and non-hypersensitivity groups. Hypersensitivity data were classified using the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0, categorizing grades from 1 to 5 as mild/moderate/severe/life-threatening/death. Multiple logistic regression analysis was used to analyze risk factors of HRs. The Cox proportional hazard regression model was used to determine the factors of being significantly associated with overall survival.
Of the 222 patients, eight exhibited HRs (incidence rate, 3.6%). All HRs were of grade 3 or 4 (life-threatening). In all cases, a desensitization protocol was followed. Advanced stage (III or IV) (P = 0.022), previous history of carboplatin use (P < 0.001), and recurrent ovarian cancer (P = 0.001) were significantly associated with HR to carboplatin. Multivariate logistic analysis showed that a previous history of carboplatin was the only independent risk factor for carboplatin-related hypersensitivity (OR, 20.19; 95% CI 1.22 - 3034.10; P = 0.034). However, HR to carboplatin did not influence the overall survival (P = 0.526).
In EOC patients, prior use of carboplatin was an independent risk factor for carboplatin-related HRs; HRs to carboplatin did not influence the overall survival. Clinicians should not underestimate the possibility risk of carboplatin HSRs when re-administrating carboplatin in EOC patients.
本研究旨在确定卡铂相关性过敏反应(HRs)的预测风险因素,并探讨其对上皮性卵巢癌(EOC)患者生存结局的影响。
本回顾性研究纳入了 2016 年 7 月至 2019 年 11 月期间接受卡铂输注的 222 例 EOC 患者。我们比较了卡铂相关性过敏反应和非过敏反应组的临床病理特征和生存结局。过敏反应数据采用不良事件通用术语标准(CTCAE)版本 5.0 进行分类,将等级分为 1-5 级,分别表示轻度/中度/重度/危及生命/死亡。采用多因素逻辑回归分析卡铂 HRs 的风险因素。采用 Cox 比例风险回归模型确定与总生存显著相关的因素。
在 222 例患者中,有 8 例出现 HRs(发生率为 3.6%)。所有 HRs 均为 3 级或 4 级(危及生命)。所有病例均采用脱敏方案。晚期(III 期或 IV 期)(P=0.022)、既往使用卡铂(P<0.001)和复发性卵巢癌(P=0.001)与卡铂相关性 HR 显著相关。多因素逻辑分析显示,既往使用卡铂是卡铂相关性 HR 的唯一独立危险因素(OR,20.19;95%CI,1.22-3034.10;P=0.034)。然而,卡铂 HR 对总生存无影响(P=0.526)。
在 EOC 患者中,既往使用卡铂是卡铂相关性 HRs 的独立危险因素;卡铂 HR 对总生存无影响。当重新给予 EOC 患者卡铂时,临床医生不应低估卡铂 HSRs 的可能性风险。