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KRAS 野生型转移性结直肠癌三线治疗中伊立替康联合西妥昔单抗再挑战的 II 期研究:JACCRO CC-08。

Phase 2 study of irinotecan plus cetuximab rechallenge as third-line treatment in KRAS wild-type metastatic colorectal cancer: JACCRO CC-08.

机构信息

Department of Clinical Oncology, Aichi Cancer Center Hospital, 1-1 Kanokoden, Chikusa-ku, Nagoya, Aichi, 464-8681, Japan.

Department of Gastroenterology, Tsuchiura Kyodo General Hospital, 1-1, Ootsuno, Tsuchiura, Ibaraki, 300-0028, Japan.

出版信息

Br J Cancer. 2020 Nov;123(10):1490-1495. doi: 10.1038/s41416-020-01042-w. Epub 2020 Aug 31.

Abstract

BACKGROUND

Regorafenib or trifluridine/tipiracil as third-line treatment have limited efficacy in metastatic colorectal cancer (mCRC).

METHODS

This Phase 2 trial evaluated the efficacy and safety of irinotecan plus cetuximab rechallenge as third-line treatment in KRAS wild-type mCRC patients who achieved clinical benefit with first-line cetuximab-containing therapy. The primary endpoint was 3-month progression-free survival (PFS) rate. A sample size was calculated; 30 patients with a 3-month PFS rate of 45% deemed promising and 15% unacceptable. Patients with greater and less than the cut-off value of cetuximab-free intervals (CFIs) were classified into the long and short CFI groups, respectively, in subgroup analyses.

RESULTS

Among 34 eligible patients who received treatment at least once, 3-month PFS rate was 44.1% (95% confidence interval, 27.4-60.8%). The median PFS and overall survival (OS) were 2.4 and 8.2 months, respectively. The response and disease control rates were 2.9 and 55.9%, respectively. PFS and OS were significantly longer in the long- than in the short CFI group.

CONCLUSIONS

Irinotecan plus cetuximab rechallenge as third-line treatment for KRAS wild-type mCRC was safe and had promising activity, especially in those with a long CFI, warranting further investigation in a Phase 3 randomised trial.

CLINICAL TRIAL REGISTRATION

UMIN000010638.

摘要

背景

瑞戈非尼或曲氟尿苷/替匹嘧啶作为三线治疗在转移性结直肠癌(mCRC)中的疗效有限。

方法

这项 2 期试验评估了伊立替康联合西妥昔单抗再挑战作为一线西妥昔单抗治疗获益的 KRAS 野生型 mCRC 患者三线治疗的疗效和安全性。主要终点是 3 个月无进展生存期(PFS)率。计算了样本量;30 例 3 个月 PFS 率为 45%的患者被认为有希望,15%的患者被认为不可接受。在亚组分析中,将无西妥昔单抗间隔时间(CFI)大于和小于截止值的患者分别分为长 CFI 组和短 CFI 组。

结果

在至少接受一次治疗的 34 例合格患者中,3 个月 PFS 率为 44.1%(95%置信区间,27.4-60.8%)。中位 PFS 和总生存期(OS)分别为 2.4 个月和 8.2 个月。缓解率和疾病控制率分别为 2.9%和 55.9%。长 CFI 组的 PFS 和 OS 明显长于短 CFI 组。

结论

伊立替康联合西妥昔单抗再挑战作为 KRAS 野生型 mCRC 的三线治疗是安全的,具有良好的活性,尤其是在 CFI 较长的患者中,值得进一步进行 3 期随机试验。

临床试验注册

UMIN000010638。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1068/7652864/46bea117ed29/41416_2020_1042_Fig1_HTML.jpg

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