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
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

103663

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Auteurs

Aristeidis E Boukouris (AE)

First Department of Internal Medicine, Korgialeneion-Benakeion General Hospital, Athens, Greece. Electronic address: arisbouk@gmail.com.

Maria Theochari (M)

First Department of Medicine, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece. Electronic address: mtheochari@gmail.com.

Dimitra Stefanou (D)

First Department of Medicine, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece. Electronic address: dimitroulastef@hotmail.com.

Alexandros Papalambros (A)

First Department of Surgery, Laikon General Hospital, School of Medicine, National Kapodistrian University of Athens, Athens, Greece. Electronic address: a_papalampros@hotmail.com.

Evangelos Felekouras (E)

First Department of Surgery, Laikon General Hospital, School of Medicine, National Kapodistrian University of Athens, Athens, Greece. Electronic address: felek@med.uoa.gr.

Helen Gogas (H)

First Department of Medicine, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece. Electronic address: helgogas@gmail.com.

Dimitrios C Ziogas (DC)

First Department of Medicine, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece. Electronic address: ziogasdc@gmail.com.

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Classifications MeSH