Latest evidence on immune checkpoint inhibitors in metastatic colorectal cancer: A 2022 update.
Anti-CTLA4
Anti-PD-1/PD-L1
Deficient MMR/microsatellite instability-high (dMMR/MSI-H)
Immune-checkpoint inhibitors
Immunotherapy
Metastatic colorectal cancer
Mismatch repair-proficient/microsatellite stable (pMMR/MSS)
Journal
Critical reviews in oncology/hematology
ISSN: 1879-0461
Titre abrégé: Crit Rev Oncol Hematol
Pays: Netherlands
ID NLM: 8916049
Informations de publication
Date de publication:
May 2022
May 2022
Historique:
received:
24
01
2022
revised:
21
03
2022
accepted:
22
03
2022
pubmed:
31
3
2022
medline:
3
5
2022
entrez:
30
3
2022
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 35351582
pii: S1040-8428(22)00087-7
doi: 10.1016/j.critrevonc.2022.103663
pii:
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
Immune Checkpoint Inhibitors
0
Ipilimumab
0
dostarlimab
0
Nivolumab
31YO63LBSN
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
103663Informations de copyright
Copyright © 2022 Elsevier B.V. All rights reserved.