微卫星不稳定性
免疫疗法
结直肠癌
医学
癌症
肿瘤科
癌症研究
癌症免疫疗法
内科学
微卫星
生物
遗传学
基因
等位基因
作者
Rong Li,Yanping Lin,Xin Shen,Jianming Guo,Ya Zhang,Jiaqi Tang,Lin Xie,Feiran Hu
标识
DOI:10.3389/fonc.2025.1636122
摘要
Background Although immune checkpoint inhibitors (ICIs) have achieved remarkable progress in the treatment of deficient mismatch repair (dMMR)/high microsatellite instability (MSI-H) colorectal cancer (CRC), nearly 50% of dMMR/MSI-H CRC patients exhibit primary resistance to immunotherapy. Case summary An 84-year-old male patient was diagnosed with poorly differentiated adenocarcinoma of the right hemicolon (pT3N2M1c, stage IVc, dMMR). The patient underwent palliative surgery of the right hemicolon and subsequently received 3 cycles of bevacizumab in combination with capecitabine. Genetic testing revealed MSI-H/TMB-H/HLA heterozygosity. When the patient came to our center for treatment, we adjusted the treatment regimen to tislelizumab immunotherapy for 4 cycles. After immunotherapy, a CT review revealed disease progression. Moreover, the patient’s physical strength deteriorated dramatically, with an Eastern Cooperative Oncology Group (ECOG) score of 3. The patient subsequently received best supportive care. The patient’s overall survival (OS) was 9 months. Conclusion The continued success of immunotherapy in dMMR/MSI-H CRC faces challenges related to immune resistance. Further studies are needed to uncover the mechanisms, targets, and biomarkers involved.
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