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雷替曲塞化疗方案联合贝伐珠单抗二线治疗转移性结直肠癌:一项前瞻性多中心 II 期试验。

Raltitrexed Chemotherapy Regimen Plus Bevacizumab as Second-Line Treatment for Metastatic Colorectal Cancer: A Prospective Multicenter Phase II Trial.

机构信息

Medical Oncology Department, Jiangsu Institute of Cancer Research, The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China.

Department of Oncology, The First Affiliated Hospital of Soochow University, Soochow, China.

出版信息

Cancer Control. 2024 Jan-Dec;31:10732748241275012. doi: 10.1177/10732748241275012.

Abstract

OBJECTIVES

Clinical studies have shown that bevacizumab plus chemotherapy significantly improves efficacy in metastatic colorectal cancer (mCRC). This prospective study aims to investigate the efficacy and safety of changing second-line treatment to raltitrexed-based chemotherapy regimens plus bevacizumab in mCRC patients who have failed the first-line fluorouracil-based chemotherapy regimen with or without bevacizumab/cetuximab.

METHODS

This is a prospective, open-label, multicenter, phase II clinical study. A total of 100 patients with mCRC after failure of the first-line fluorouracil-based chemotherapy regimen with or without bevacizumab/cetuximab were enrolled from November 2016 to October 2021, and received second-line raltitrexed-based chemotherapy regimen plus bevacizumab. Patients were treated for 6 cycles, and efficacy evaluation over stable disease were followed by maintenance treatment of bevacizumab and raltitrexed until disease progression or intolerable toxicity. The primary endpoint was progression-free survival (PFS). Secondary endpoints included overall survival (OS), objective response rate (ORR), disease control rate (DCR), safety, and toxicity.

RESULTS

Ninety-four patients were treated with SALIRI (raltitrexed + irinotecan) plus bevacizumab, and six patients with SALOX (raltitrexed + oxaliplatin) plus bevacizumab. Median PFS was 8.4 (95% CI: 6.2-11.0) months, including 8.2 (95% CI 6.2, 11.0) months in the SALIRI group and 11.6 (95% CI 3.1, NA) months in the SALOX group. Median OS was 17.6 (95% CI 15.2, 22.0) months in the SALIRI group and 17.1 (95% CI 4.1, NA) months in the SALOX group. ORR and DCR were 25.5% and 87.2% in the SALIRI group, and 33.3% and 83.3% in the SALOX group, respectively. A low incidence of grade 3-4 adverse events was observed.

CONCLUSIONS

Raltitrexed-based chemotherapy regimens plus bevacizumab improved survival duration in mCRC patients with failed first-line therapy. Therefore, treatment with raltitrexed-based chemotherapy regimens plus bevacizumab could be a superior therapeutic option for second-line chemotherapy in mCRC (ClinicalTrials.gov registration number: NCT03126071).

摘要

目的

临床研究表明,贝伐珠单抗联合化疗显著提高转移性结直肠癌(mCRC)的疗效。本前瞻性研究旨在探讨在一线氟尿嘧啶类化疗方案联合或不联合贝伐珠单抗/西妥昔单抗治疗失败的 mCRC 患者中,二线改用雷替曲塞为基础的化疗方案联合贝伐珠单抗的疗效和安全性。

方法

这是一项前瞻性、开放标签、多中心、II 期临床研究。共纳入 2016 年 11 月至 2021 年 10 月 100 例一线氟尿嘧啶类化疗方案联合或不联合贝伐珠单抗/西妥昔单抗治疗失败的 mCRC 患者,二线采用雷替曲塞为基础的化疗方案联合贝伐珠单抗。患者接受 6 个周期的治疗,稳定疾病的疗效评估后,继续使用贝伐珠单抗和雷替曲塞维持治疗,直至疾病进展或无法耐受毒性。主要终点为无进展生存期(PFS)。次要终点包括总生存期(OS)、客观缓解率(ORR)、疾病控制率(DCR)、安全性和毒性。

结果

94 例患者接受 SALIRI(雷替曲塞+伊立替康)联合贝伐珠单抗治疗,6 例患者接受 SALOX(雷替曲塞+奥沙利铂)联合贝伐珠单抗治疗。中位 PFS 为 8.4 个月(95%CI:6.2-11.0),其中 SALIRI 组为 8.2 个月(95%CI 6.2,11.0),SALOX 组为 11.6 个月(95%CI 3.1,NA)。中位 OS 为 17.6 个月(95%CI 15.2,22.0),其中 SALIRI 组为 17.1 个月(95%CI 4.1,NA),SALOX 组为 17.1 个月(95%CI 4.1,NA)。SALIRI 组的 ORR 和 DCR 分别为 25.5%和 87.2%,SALOX 组分别为 33.3%和 83.3%。观察到 3-4 级不良事件发生率较低。

结论

雷替曲塞为基础的化疗方案联合贝伐珠单抗可延长一线治疗失败的 mCRC 患者的生存时间。因此,雷替曲塞为基础的化疗方案联合贝伐珠单抗可能是 mCRC 二线化疗的更佳治疗选择(ClinicalTrials.gov 注册号:NCT03126071)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2435/11423381/f1e976e665f3/10.1177_10732748241275012-fig1.jpg

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