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免疫治疗时代前错配修复缺陷转移性结直肠癌患者的生存情况。

Survival of patients with deficient mismatch repair metastatic colorectal cancer in the pre-immunotherapy era.

机构信息

Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, Universiteitsweg 100, 3584CG, Utrecht, The Netherlands.

Department of Research, Netherlands Comprehensive Cancer Organisation, Postbus 19079, 3501DB, Utrecht, The Netherlands.

出版信息

Br J Cancer. 2021 Jan;124(2):399-406. doi: 10.1038/s41416-020-01076-0. Epub 2020 Oct 13.

DOI:10.1038/s41416-020-01076-0
PMID:33046804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7852682/
Abstract

BACKGROUND

Metastatic colorectal cancer patients with deficient mismatch repair (dMMR mCRC) benefit from immunotherapy. Interpretation of the single-arm immunotherapy trials is complicated by insignificant survival data during systemic non-immunotherapy. We present survival data on a large, comprehensive cohort of dMMR mCRC patients, treated with or without systemic non-immunotherapy.

METHODS

Two hundred and eighty-one dMMR mCRC patients (n = 54 from three prospective Phase 3 CAIRO trials; n = 227 from the Netherlands Cancer Registry). Overall survival was analysed from diagnosis of mCRC (OS), from initiation of first-line (OS1) and second-line (OS2) systemic treatment. Cox regression analysis examined prognostic factors. As comparison for OS 2746 MMR proficient mCRC patients were identified.

RESULTS

Of 281 dMMR patients, 62% received first-line and 26% second-line treatment. Median OS was 16.0 months (13.8-19.6) with antitumour therapy and 2.5 months (1.8-3.5) in untreated patients. OS1 was 12.8 months (10.7-15.2) and OS2 6.2 months (5.4-8.9) in treated dMMR patients. Treated dMMR patients had a 7.6-month shorter median OS than pMMR patients.

CONCLUSION

Available data from immunotherapy trials lack a control arm with standard systemic treatment. Given the poor outcome compared to the immunotherapy results, our data strongly suggest a survival benefit of immunotherapy in dMMR mCRC patients.

摘要

背景

错配修复缺陷(dMMR)转移性结直肠癌(mCRC)患者受益于免疫治疗。由于系统非免疫治疗期间生存数据无显著差异,因此对单臂免疫治疗试验的解释较为复杂。我们提供了大量 dMMR mCRC 患者的生存数据,这些患者接受或未接受系统非免疫治疗。

方法

281 名 dMMR mCRC 患者(n=54 名来自三项前瞻性 3 期 CAIRO 试验;n=227 名来自荷兰癌症登记处)。从 mCRC(OS)诊断、一线(OS1)和二线(OS2)全身治疗开始时分析总生存。Cox 回归分析检查了预后因素。作为 OS2 的比较,鉴定了 2746 名 MMR 正常的 mCRC 患者。

结果

281 名 dMMR 患者中,62%接受一线治疗,26%接受二线治疗。有抗肿瘤治疗的中位 OS 为 16.0 个月(13.8-19.6),未治疗患者为 2.5 个月(1.8-3.5)。接受治疗的 dMMR 患者的 OS1 为 12.8 个月(10.7-15.2),OS2 为 6.2 个月(5.4-8.9)。与 pMMR 患者相比,接受治疗的 dMMR 患者的中位 OS 缩短了 7.6 个月。

结论

免疫治疗试验的现有数据缺乏标准系统治疗的对照臂。鉴于与免疫治疗结果相比预后较差,我们的数据强烈提示免疫治疗在 dMMR mCRC 患者中有生存获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12ba/7852682/b4dad755f2b3/41416_2020_1076_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12ba/7852682/dc70e5dea615/41416_2020_1076_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12ba/7852682/b4dad755f2b3/41416_2020_1076_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12ba/7852682/dc70e5dea615/41416_2020_1076_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12ba/7852682/b4dad755f2b3/41416_2020_1076_Fig2_HTML.jpg

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