Evidence map›Paper›PMID 41969588›Full record

ArticleOncology letters2026

Immunotherapy-based treatment patterns and clinical outcomes across lines of therapy in microsatellite stable metastatic colorectal cancer: A real-world study.

Wen-Si Zhao, Shi-Jing Ma, Tao Zhang, De-Dong Cao

Abstract read
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Article in Oncology letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Wen-Si ZhaoDepartment of Oncology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430060, P.R. China.
Shi-Jing MaDepartment of Geriatrics, Renmin Hospital of Wuhan University, Wuhan, Hubei 430060, P.R. China.
Tao ZhangDepartment of Oncology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, P.R. China.
De-Dong CaoDepartment of Oncology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430060, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microsatellite stable (MSS) metastatic colorectal cancer (mCRC) hardly benefits from immune-monotherapy. Immune checkpoint inhibitor (ICI)-based combinations have been explored with mixed results. To evaluate the treatment patterns and outcomes across lines of immunotherapy in MSS mCRC, a retrospective real-world data analysis was performed in the present study. A total of 202 patients treated at Renmin Hospital of Wuhan University from June 2019 to December 2023 were included in the analysis, encompassing 38, 41 and 123 cases that received first-(1L), second-(2L) and third-line or above (3L+) ICI-based therapies, respectively. ICI combined with chemotherapy, ICI combined with chemotherapy and anti-VEGF(R)/EGFR/HER2 monoclonal antibody, and ICI combined with tyrosine kinase inhibitor (TKI) were the main options for the 1L, 2L and 3L+ cohorts, respectively. The objective response rates of the 1L, 2L and 3L+ treatment cohorts were 63.2, 22.0 and 11.4%, respectively, and the disease control rates of these three cohorts were 94.7, 75.6 and 70.7%, respectively. The median progression-free survival of the 1L, 2L and 3L+ cohorts was 11.1, 6.5 and 4.7 months, respectively, and overall survival (OS) was not reached, 16.0 and 11.9 months, respectively. After propensity score matching, patients who received ICI cross-line therapy at least once in the 3L+ cohort showed directional OS improvement (14.3 vs. 11.3 months; hazard ratio, 0.66; 95% confidence interval, 0.39-1.14; P=0.123) compared with those who did not receive ICI cross-line therapy. Grade ≥3 adverse events (AEs) occurred in 43.6% of patients, with thrombocytopenia, leukopenia and abnormal hepatic function being the most common. The incidence of immune-related AEs (irAEs) was 38.6% and that of grade ≥3 irAEs was 15.3%. These findings suggest that chemotherapy remains the cornerstone of 1L and 2L treatment for MSS mCRC, while the combination of ICI and TKI has developed into a major trend at the 3L+ setting with improved survival and controllable safety.

Indexed as

immune checkpoint inhibitormetastatic colorectal cancermicrosatellite stableoverall survivalreal-world study

Identifiers

PMID41969588
PMCPMC13062620

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.