无容量
彭布罗利珠单抗
医学
易普利姆玛
微卫星不稳定性
结直肠癌
肿瘤科
内科学
免疫疗法
临床试验
免疫检查点
癌症
生物
等位基因
基因
微卫星
生物化学
作者
Aristeidis E. Boukouris,Maria Theochari,Dimitra Stefanou,Alexandros Papalambros,Evangelos Felekouras,Helen Gogas,Dimitrios C. Ziogas
标识
DOI:10.1016/j.critrevonc.2022.103663
摘要
The long-term remissions induced by immune-checkpoint inhibitors (ICIs) in many types of cancers have opened up the possibility of a broader use of immunotherapy in less immunogenic but genetically heterogeneous tumours. Regarding metastatic colorectal cancer (mCRC), in first-line setting, pembrolizumab has been approved as preferred option and nivolumab, alone or in combination with ipilimumab as alternative option for patients with mismatch-repair-deficient and microsatellite instability-high (dMMR/MSI-H) disease, independently of their eligibility for intensive chemotherapy. In subsequent lines, both these immunotherapeutic regimens (e.g., pembrolizumab and nivolumab+/-ipilimumab) as well as dostarlimab-gxly are currently recommended for patients with dMMR/MSI-H chemo-resistant mCRC who have not previously received an ICI. Beginning from the rationale behind the immune-mediated interplay in the dMMR/MSI-H bowel microenvironment, we provide here an update on the evolution status of all available, approved or not, ICIs in mCRC, describing their efficacy and toxicity profile with an emphasis on the pivotal trials supporting current colorectal indications. For each ICI agent, the results from combinations under investigation, particularly for those being upgraded in clinical phasing, the perspectives but also the limitations of main ongoing trials are thoroughly discussed. In the close future, upcoming data are expected to confirm the clinical benefit of ICIs and to further expand their role in mCRC.
科研通智能强力驱动
Strongly Powered by AbleSci AI