降压治疗对辅助贝伐单抗治疗卵巢癌(IATRO)结局的影响,来自全国模拟临床试验的结果。

IF 5.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Floriane Jochum, Élise Dumas, Joe-Elie Salem, Stéphane Ederhy, Anne-Sophie Hamy, Lise Lecointre, Enora Laas, Fabien Reyal, Fabrice Lecuru, Cherif Akladios, Paul Gougis
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引用次数: 0

摘要

贝伐单抗抗血管生成治疗改善卵巢癌的预后,但诱发高血压,导致主要不良心血管事件(MACE)。虽然钙通道阻滞剂(CCBs)和血管紧张素转换酶抑制剂(ACEi)被推荐用于治疗贝伐单抗相关性高血压,但它们对癌症进展和心血管结局的影响尚不清楚。本研究比较了CCBs和ACEi对辅助贝伐单抗治疗的卵巢癌患者无进展生存期(PFS)的影响。同时评估MACE发生率和总生存期(OS)。我们使用法国国家健康数据系统(SNDS) 2011年1月1日至2021年1月1日的数据进行了一项模拟临床试验,覆盖了法国人口的98.8%。FIGO III至IV期卵巢癌患者在术后6个月内接受了细胞减少手术和贝伐单抗辅助化疗,并接受CCBs或ACEi单药治疗。在接受贝伐单抗治疗的4165例患者中,454例符合主要分析的纳入标准:CCBs组273例,ACEi组181例。与ACEi相比,CCBs的使用与更长的中位PFS(21.8个月对18.2个月)和更高的3年PFS率相关(差异为8.2个百分点,95% CI: 2.0%; 14.8%)。两组间OS无明显差异。与ACEi相比,CCBs的心血管并发症更频繁,尤其是充血性心力衰竭(3年MACE发生率差异:-4.5个百分点;95% CI: -8.2%; -1.1%)。这些研究结果强调需要一个平衡的方法来管理癌症患者的高血压,同时考虑肿瘤和心脏预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Antihypertensive Treatment on Outcomes of Adjuvant Bevacizumab for Ovarian Cancer (IATRO), Results from a Nationwide Emulated Clinical Trial.

Antiangiogenic therapy with bevacizumab improves outcomes in ovarian cancer but induces hypertension, leading to major adverse cardiovascular events (MACE). While calcium channel blockers (CCBs) and angiotensin-converting enzyme inhibitors (ACEi) are recommended for managing bevacizumab-associated hypertension, their impacts on cancer progression and cardiovascular outcomes are unclear. This study compared the effects of CCBs and ACEi on progression-free survival (PFS) in ovarian cancer patients treated with adjuvant bevacizumab. The incidence of MACE and overall survival (OS) were also evaluated. We conducted an emulated clinical trial using data from January 1, 2011, to January 1, 2021, from the French National Health Data System (SNDS), covering 98.8% of the French population. Patients with FIGO stage III to IV ovarian cancer who underwent cytoreductive surgery and adjuvant chemotherapy with bevacizumab, treated with CCBs or ACEi monotherapy within 6 months after surgery, were included. Out of 4,165 patients treated with bevacizumab, 454 met inclusion criteria for the main analysis: 273 in the CCBs group and 181 in the ACEi group. CCBs use was associated with a longer median PFS compared to ACEi (21.8 vs. 18.2 months) and a higher 3-year PFS rate (difference of 8.2 percentage points, 95% CI: 2.0%; 14.8%). No significant difference in OS was observed between groups. Cardiovascular complications were more frequent with CCBs compared to ACEi, particularly congestive heart failure (difference in 3-year incidence of MACE: -4.5 percentage points; 95% CI: -8.2%; -1.1%). These findings emphasize the need for a balanced approach to managing hypertension in cancer patients, considering both oncologic and cardiologic outcomes.

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来源期刊
CiteScore
12.70
自引率
7.50%
发文量
290
审稿时长
2 months
期刊介绍: Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.
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