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Clin Cancer Res. 2022 Oct 3;28(19):4186-4193. doi: 10.1158/1078-0432.CCR-21-1733.
2
Randomized phase II trial of weekly paclitaxel vs. cediranib-olaparib (continuous or intermittent schedule) in platinum-resistant high-grade epithelial ovarian cancer.每周一次紫杉醇对比西地尼布-奥拉帕利(持续或间歇给药方案)治疗铂耐药高级别上皮性卵巢癌的随机II期试验
Gynecol Oncol. 2022 Mar;164(3):505-513. doi: 10.1016/j.ygyno.2022.01.015. Epub 2022 Jan 19.
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Atezolizumab, Bevacizumab, and Chemotherapy for Newly Diagnosed Stage III or IV Ovarian Cancer: Placebo-Controlled Randomized Phase III Trial (IMagyn050/GOG 3015/ENGOT-OV39).阿替利珠单抗、贝伐珠单抗联合化疗治疗新诊断的 III 期或 IV 期卵巢癌:安慰剂对照随机 III 期试验(IMagyn050/GOG 3015/ENGOT-OV39)。
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血管内皮生长因子抑制剂在治疗上皮性卵巢癌中的作用。

The role of vascular endothelial growth factor inhibitors in the treatment of epithelial ovarian cancer.

机构信息

The Christie NHS Foundation Trust, Manchester, M20 4BX, UK.

Division of Cancer Sciences, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, UK.

出版信息

Br J Cancer. 2022 Apr;126(6):851-864. doi: 10.1038/s41416-021-01605-5. Epub 2021 Oct 29.

DOI:10.1038/s41416-021-01605-5
PMID:34716396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8927157/
Abstract

Advanced epithelial ovarian, fallopian tube and primary peritoneal cancers (EOC) are a leading cause of gynaecological cancer-associated mortality and angiogenesis plays a key role in their growth. Vascular endothelial growth factor inhibitors (VEGFi) disrupt angiogenesis and improve the response rate, progression-free survival and in some cases, overall survival, when administered with and following cytotoxic chemotherapy, irrespective of the platinum sensitivity of EOC. Recent data have identified new indications for VEGFi in EOC: repeated exposure to VEGFi in the first- and then second-line treatment has sustained clinical efficacy; combinations of VEGFi with poly (ADP-ribose) polymerase inhibitors (PARPi) have proven effective as first-line or second-line maintenance regimens. However, recent trial data have not shown improved outcomes with combinations of VEGFi and immune checkpoint inhibitors. There remains a critical need to optimise patient selection for these effective yet somewhat toxic and expensive treatments. The search continues for validated biomarkers to optimise the use of VEGFi, of which the most promising at present is plasma Tie2. Based upon these studies, we propose a model of care incorporating VEGFi into the treatment of EOC, highlighting the need to change from the prescription of single courses of VEGFi, to allow use and re-use as clinically indicated.

摘要

高级上皮性卵巢癌、输卵管癌和原发性腹膜癌(EOC)是妇科癌症相关死亡的主要原因,血管生成在其生长中起着关键作用。血管内皮生长因子抑制剂(VEGFi)可破坏血管生成,并在与细胞毒性化疗联合使用或之后提高反应率、无进展生存期,在某些情况下还能提高总生存期,而不论 EOC 的铂类敏感性如何。最近的数据确定了 VEGFi 在 EOC 中的新适应证:在一线和二线治疗中反复暴露于 VEGFi 可维持临床疗效;VEGFi 与聚 ADP-核糖聚合酶抑制剂(PARPi)联合使用已被证明作为一线或二线维持方案有效。然而,最近的试验数据并未显示 VEGFi 与免疫检查点抑制剂联合使用可改善结局。对于这些有效但毒性和费用较高的治疗方法,仍迫切需要优化患者选择。目前正在寻找经过验证的生物标志物来优化 VEGFi 的使用,其中最有前途的是血浆 Tie2。基于这些研究,我们提出了一种将 VEGFi 纳入 EOC 治疗的护理模式,强调需要从单一疗程的 VEGFi 处方转变为根据临床需要允许使用和重复使用。