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在最大程度减瘤的卵巢癌患者中腹腔化疗的依从性和不良事件:真实研究。

Adherence and adverse events of intraperitoneal chemotherapy in optimally debulked ovarian cancer patients: Real-life study.

机构信息

Servicio de Farmacia, Área del Medicamento, Hospital Universitari i Politècnic La Fe, Valencia, Spain.

Servicio de Oncología Médica, Hospital Universitari i Politècnic La Fe, Valencia, Spain.

出版信息

J Oncol Pharm Pract. 2021 Mar;27(2):268-278. doi: 10.1177/1078155220915953. Epub 2020 Apr 11.

Abstract

PURPOSE

Intraperitoneal with intravenous chemotherapy (IP/IV) is the recommended option for patients with stage III cancer with optimally debulked (<1 cm residual) disease based on randomized controlled trials and showing important improvements in overall survival and progression free survival. However, its application has not been largely adopted due to its difficult administration that requires a trained nurse staff. The aim of this work was to study the completion and the toxicity of an IP outpatient chemotherapy regimen in optimally debulked stage III ovarian cancer patients.

METHODS

A single-center, retrospective observational study in women with stage III ovarian cancer following optimal cytoreductive surgery (<1 cm) followed by IP/IV chemotherapy from 2009 to 2017. The IP/IV regimen was as it follows: IV paclitaxel 175 mg/m in 3 h, day 1; IP cisplatin (100 mg/m-until December 2013-or 75 mg/m), day 2; IP paclitaxel 60 mg/m, day 8, each 21 days for six cycles.

RESULTS

A total of 60 patients received IP/IV regimen. Of these, 41 patients (68.3%) completed the six IP chemotherapy cycles and 51 (84.9%) completed four or more cycles. Most of the adverse events reported were non-hematological and G1-2. There was no difference neither in adherence nor in the frequency of adverse events between both cisplatin groups. Despite a high rate of adverse events, IP chemotherapy can be delivered with a high completion rate and manageable toxicity to patients with optimally debulked ovarian cancer.

摘要

目的

基于随机对照试验,对于最大程度减瘤(残余肿瘤<1cm)的 III 期癌症患者,腹腔内联合静脉化疗(IP/IV)是推荐的选择,其在总生存期和无进展生存期方面显示出重要的改善。然而,由于其需要经过培训的护士人员来管理,因此其应用并未得到广泛采用。本研究旨在研究在最大程度减瘤的 III 期卵巢癌患者中进行 IP 门诊化疗方案的完成情况和毒性。

方法

一项单中心、回顾性观察研究,纳入 2009 年至 2017 年间接受过最佳减瘤手术(<1cm)后接受 IP/IV 化疗的 III 期卵巢癌女性患者。IP/IV 方案如下:静脉滴注紫杉醇 175mg/m,3 小时,第 1 天;腹腔内顺铂(100mg/m-直至 2013 年 12 月-或 75mg/m),第 2 天;腹腔内紫杉醇 60mg/m,第 8 天,每 21 天为一个周期,共 6 个周期。

结果

共有 60 例患者接受了 IP/IV 方案治疗。其中,41 例(68.3%)完成了 6 个 IP 化疗周期,51 例(84.9%)完成了 4 个或更多周期。报告的大多数不良事件是非血液学的,G1-2 级。在顺铂两个剂量组中,依从性和不良事件的频率均无差异。尽管不良事件发生率较高,但对于最大程度减瘤的卵巢癌患者,IP 化疗可完成率较高,毒性可管理。

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