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卵巢癌患者接受 VEGFR-TKI 治疗后腹泻的评估和管理。

Assessment and management of diarrhea following VEGF receptor TKI treatment in patients with ovarian cancer.

机构信息

Dana-Farber Cancer Institute, Boston, MA, USA.

Department of Oncology, University of Oxford, Oxford, UK.

出版信息

Gynecol Oncol. 2018 Jul;150(1):173-179. doi: 10.1016/j.ygyno.2018.03.058. Epub 2018 Apr 5.

DOI:10.1016/j.ygyno.2018.03.058
PMID:29627080
Abstract

Angiogenesis is a proven clinical target for the treatment of advanced epithelial ovarian cancer. Vascular endothelial growth factor receptor tyrosine kinase inhibitors (VEGFR-TKIs) offer patients potential new treatment regimens as they can be given as monotherapy, in combination with poly(ADP-ribose) polymerase (PARP) inhibitors, or with and following cytotoxic chemotherapy. If VEGFR-TKIs are licensed for use in ovarian cancer, patients will require prompt and effective management of adverse events, including diarrhea, to optimize compliance and benefit. As diarrhea is one of the most prevalent toxicities of this class of drug, it is important to consider the potential causes, be they disease related (bowel obstruction), treatment related (VEGFR-TKI-related or infective/neutropenic septic diarrhea when patients are receiving cytotoxic chemotherapy combined with VEGFR inhibitor treatment), or incurred through diet. Here, we provide an overview of the possible mechanisms responsible for VEGFR-TKI-induced diarrhea. We review potential interventions that can help in the management of diarrhea induced by VEGFR-TKIs, when used in combination or as single agents, and we provide a diarrhea treatment algorithm to serve as a clinical reference point for the management of diarrhea in patients with ovarian cancer treated with a VEGFR-TKI in combination with chemotherapy or PARP inhibitors, or as monotherapy.

摘要

血管生成是治疗晚期上皮性卵巢癌的一种已被证实的临床靶点。血管内皮生长因子受体酪氨酸激酶抑制剂 (VEGFR-TKI) 为患者提供了新的潜在治疗方案,因为它们可以作为单药治疗、与聚 ADP 核糖聚合酶 (PARP) 抑制剂联合使用、与细胞毒性化疗联合使用或之后使用。如果 VEGFR-TKI 获准用于卵巢癌治疗,患者将需要及时有效地管理不良反应,包括腹泻,以优化依从性并从中获益。由于腹泻是此类药物最常见的毒性之一,因此必须考虑其潜在原因,包括与疾病相关的原因(肠阻塞)、与治疗相关的原因(当患者接受细胞毒性化疗联合 VEGFR 抑制剂治疗时,与 VEGFR-TKI 相关或感染性/中性粒细胞减少性败血症性腹泻)或因饮食引起的原因。在这里,我们概述了 VEGFR-TKI 引起腹泻的可能机制。我们回顾了在 VEGFR-TKI 联合或单药使用时可能有助于管理腹泻的潜在干预措施,并提供了腹泻治疗算法,作为联合化疗或 PARP 抑制剂或单药治疗卵巢癌患者使用 VEGFR-TKI 时管理腹泻的临床参考点。

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