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伊立替康联合雷替曲塞二线治疗局部晚期或转移性结直肠癌患者的前瞻性开放标签、单臂、多中心、II 期研究。

Irinotecan plus raltitrexed as second-line treatment in locally advanced or metastatic colorectal cancer patients: a prospective open-label, single-arm, multi-center, phase II study.

机构信息

Department of Oncology, The First Hospital of China Medical University, Shenyang, Liaoning Province, China.

Key Laboratory of Anticancer Drugs and Biotherapy of Liaoning Province, the First Hospital of China Medical University, Shenyang, Liaoning Province, China.

出版信息

BMC Cancer. 2024 Sep 2;24(1):1082. doi: 10.1186/s12885-024-12831-4.

Abstract

BACKGROUND

Colorectal cancer is the third most common cancer and the second leading cause of cancer death. There are limited therapeutic options for the treatment of locally advanced or metastatic colorectal cancers which fail first-line chemotherapy. Phase I/II studies showed that the combined application of the raltitrexed and irinotecan has significant synergistic effect and acceptable toxicity. However, most of these previous studies have relatively small sample size.

METHODS

This is a prospective open-label, single-arm, multi-center, Phase II trial. Brief inclusion criteria: patients were aged 18 to 75 years with locally advanced or metastatic colorectal cancer after failure of 5-FU and oxaliplatin therapy. Enrolled patients received raltitrexed (3 mg/m, d1) and irinotecan (180 mg/m, d1) each 21-day cycle until disease progression or unacceptable toxicity. The primary endpoint was progression-free survival, and the secondary endpoints were disease control rate, objective response rate, overall survival and safety.

RESULTS

A total of 108 patients were enrolled between September 2016 and May 2020. The median age was 61 years, ECOG 1 score accounts for 67.6%, the rest were ECOG 0. A total of 502 cycles were completed, with an average of 4.6 cycles and a median of 4 cycles. 108 patients were evaluated, with an objective response rate of 17.6%, and disease control rate of 76.9%. The median follow-up time was 27 months (range:3.1-61.0 m) at data cut-off on March 2023. Median progression-free survival was 4.9 months (95% CI 4.1-5.7) and median overall survival was 13.1 months (95% CI 12.2-15.5). The most common adverse events that were elevated are alanine aminotransferase increased, aspartate aminotransferase increased, fatigue, diarrhoea, neutrocytopenia, thrombocytopenia, hypohemoglobin, and leukocytopenia. Most of the adverse events were Grade I/II, which were relieved after symptomatic treatment, and there were no treatment-related cardiotoxicities and deaths.

CONCLUSIONS

The combination of raltitrexed and irinotecan as second-line treatment for mCRC could be a reliable option after failure of standard 5-Fu-first-line chemotherapy in locally advanced or metastatic colorectal cancers, especially for patients with 5-FU intolerance (cardiac events or DPD deficiency patients).

TRIAL REGISTRATION

ClinicalTrials.gov identifier: NCT03053167, registration date was 14/2/2017.

摘要

背景

结直肠癌是第三大常见癌症,也是癌症死亡的第二大主要原因。对于一线化疗失败的局部晚期或转移性结直肠癌,治疗选择有限。I/II 期研究表明,雷替曲塞和伊立替康联合应用具有显著的协同作用和可接受的毒性。然而,这些先前的研究大多样本量相对较小。

方法

这是一项前瞻性、开放标签、单臂、多中心、II 期试验。简要纳入标准:年龄 18-75 岁,接受 5-FU 和奥沙利铂治疗后局部晚期或转移性结直肠癌进展。入组患者每 21 天周期接受雷替曲塞(3mg/m,d1)和伊立替康(180mg/m,d1)治疗,直至疾病进展或出现不可接受的毒性。主要终点为无进展生存期,次要终点为疾病控制率、客观缓解率、总生存期和安全性。

结果

2016 年 9 月至 2020 年 5 月共纳入 108 例患者。中位年龄 61 岁,ECOG 1 评分占 67.6%,其余为 ECOG 0。共完成 502 个周期,平均 4.6 个周期,中位数 4 个周期。108 例患者进行了评估,客观缓解率为 17.6%,疾病控制率为 76.9%。中位随访时间为 2023 年 3 月数据截止时的 27 个月(范围:3.1-61.0m)。中位无进展生存期为 4.9 个月(95%CI 4.1-5.7),中位总生存期为 13.1 个月(95%CI 12.2-15.5)。最常见的升高的不良事件为丙氨酸氨基转移酶升高、天门冬氨酸氨基转移酶升高、乏力、腹泻、中性粒细胞减少症、血小板减少症、低血红蛋白血症和白细胞减少症。大多数不良事件为 1/2 级,经对症治疗后缓解,无治疗相关的心脏毒性和死亡。

结论

雷替曲塞和伊立替康联合作为局部晚期或转移性结直肠癌一线 5-FU 化疗失败后的二线治疗,特别是对 5-FU 不耐受(心脏事件或 DPD 缺乏患者)的患者,可能是一种可靠的选择。

试验注册

ClinicalTrials.gov 标识符:NCT03053167,注册日期为 2017 年 2 月 14 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bc8/11368032/fe161377178f/12885_2024_12831_Fig1_HTML.jpg

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