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