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Efficacy, Safety, and Survival Outcomes of Immune Checkpoint Inhibitors in Patients with Mismatch Repair-Deficient
Mehmet Cihan İcli1, Deniz Can Guven1, Arif Akyildiz1,2
1Department of Medical Oncology, Hacettepe University, Ankara 06100, Türkiye.
Abstract:
Background: Microsatellite instability-high (MSI-H) or mismatch repair-deficient (dMMR) colorectal cancer (CRC) accounts for approximately 5% of metastatic CRC cases. Immune checkpoint inhibitors (ICIs) are the standard of care based on pivotal clinical trials; however, real-world data, particularly from low-resource countries, remain scarce, and prognostic factors are not yet fully defined. Therefore, we evaluated the efficacy and the safety of ICIs in a multi-center cohort. Methods: This multi-center retrospective study included 45 patients treated with ICIs across six oncology centers in Türkiye between June 2017 and December 2024. Patients received either anti-PD-1/PD-L1 monotherapy or anti-CTLA-4-based combination therapy. Key clinical variables and 1-, 2-, and 3-year OS and PFS outcomes were systematically collected. Results: The median age was 61 years, and most patients (75.6%) received ICIs in later treatment lines. After a median follow-up of 24.1 months, median OS and PFS were not reached. The estimated 1-, 2-, and 3-year OS rates were 82%, 76.1%, and 76.1%; PFS rates were 75.6%, 67.5%, and 67.5%, respectively. In multivariate analysis, an ECOG < 1 (HR: 0.072; 95% CI: 0.012-0.453; p = 0.005), a metastatic burden of fewer than two sites (HR: 0.211; 95% CI: 0.052-0.860; p = 0.030), and absence of antibiotic exposure within one month prior to immunotherapy initiation (HR: 0.145; 95% CI: 0.034-0.614; p = 0.009) were independently associated with improved overall survival. For PFS, ECOG < 1 (HR: 0.172; 95% CI: 0.052-0.573; p = 0.004), a metastatic burden of fewer than two sites (HR: 0.248; 95% CI: 0.078-0.788; p = 0.018), and no recent antibiotic exposure (HR: 0.209; 95% CI: 0.064-0.687; p = 0.010) remained independent predictors of prolonged survival. Conclusions: We observed overall survival outcomes similar to those reported in phase III clinical trials of immunotherapy in MSI-H/dMMR colorectal cancer, despite a substantial proportion of patients receiving immunotherapy in later lines of treatment. These findings support immune checkpoint inhibitors as the standard of care for MSI-H/dMMR metastatic colorectal cancer and emphasize the importance of improving access to immunotherapy, particularly in low-resource settings.
Insights
Immune checkpoint inhibitors (ICIs) show promising survival outcomes in microsatellite instability-high (MSI-H) or mismatch repair-deficient (dMMR) metastatic colorectal cancer (CRC), similar to clinical trials. Key factors for improved survival include good performance status and limited metastatic sites.
Area of Science:
- Oncology
- Immunotherapy
- Gastroenterology
Background:
- Microsatellite instability-high (MSI-H) or mismatch repair-deficient (dMMR) colorectal cancer (CRC) represents a distinct subtype of metastatic disease.
- Immune checkpoint inhibitors (ICIs) are established treatments, but real-world data, especially from resource-limited regions, are scarce.
- Prognostic factors influencing ICI efficacy in this population require further definition.
Purpose of the Study:
- To evaluate the real-world efficacy and safety of ICIs in a multi-center cohort of MSI-H/dMMR metastatic CRC patients.
- To identify prognostic factors associated with improved overall survival (OS) and progression-free survival (PFS).
Main Methods:
- A retrospective multi-center study involving 45 patients treated with ICIs (anti-PD-1/PD-L1 or anti-CTLA-4 based) in Türkiye.
- Systematic collection of clinical variables and 1-, 2-, and 3-year OS and PFS outcomes.
- Multivariate analysis to identify independent predictors of survival.
Main Results:
- The cohort had a median age of 61 years, with 75.6% receiving ICIs in later treatment lines.
- Estimated 1-, 2-, and 3-year OS rates were 82%, 76.1%, and 76.1%, respectively; PFS rates were 75.6%, 67.5%, and 67.5%.
- Independent predictors of improved OS and PFS included ECOG performance status < 1, fewer than two metastatic sites, and no recent antibiotic exposure.
Conclusions:
- Real-world ICI outcomes in MSI-H/dMMR metastatic CRC mirror phase III trial results, even with later-line treatment.
- ICIs are confirmed as standard of care for MSI-H/dMMR metastatic CRC.
- Enhancing access to immunotherapy, particularly in low-resource settings, is crucial.
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