Clinically applicable cases of anti-programmed cell death protein 1 immunotherapy for colorectal cancer patients.
Aged
Antibodies, Monoclonal, Humanized
/ administration & dosage
Brain Neoplasms
Colorectal Neoplasms
/ genetics
DNA Mismatch Repair
Digestive System Surgical Procedures
/ methods
Female
Genetic Counseling
Genetic Testing
Humans
Immunotherapy
/ methods
Male
Neoplasm Staging
Neoplastic Syndromes, Hereditary
Programmed Cell Death 1 Receptor
Anti-PD-1 blockade
Colorectal cancer
Defective mismatch repair
Journal
Surgery today
ISSN: 1436-2813
Titre abrégé: Surg Today
Pays: Japan
ID NLM: 9204360
Informations de publication
Date de publication:
Dec 2020
Dec 2020
Historique:
received:
04
12
2019
accepted:
17
03
2020
pubmed:
8
4
2020
medline:
27
4
2021
entrez:
8
4
2020
Statut:
ppublish
Résumé
We investigated the prevalence and characteristics of defective mismatch repair (dMMR) in colorectal cancer (CRC) patients who would potentially benefit from anti-programmed cell death protein 1 (PD-1) immunotherapy. Medical records were obtained and reviewed for 1147 patients who underwent surgical resection of stage I-IV CRC, in whom universal screening for Lynch syndrome using immunohistochemistry for MMR proteins had been undertaken. The molecular characteristics of dMMR CRCs were also investigated. Defective MMR accounted for 5.2% of stage I-IV CRC patients, including 12 (1.0% of all CRC patients) who had stage IV disease or recurrence after curative resection (n = 6 each). These 12 patients included patients with LS (n = 3) and Lynch-like syndrome (n = 1). Defective MMR tumors were predominantly located in the right-sided colon (P < 0.01). Approximately 1% of stage I-IV CRC patients could potentially benefit from anti-PD-1 immunotherapy, while one-third would require genetic counseling and/or MMR gene testing.
Identifiants
pubmed: 32253514
doi: 10.1007/s00595-020-01998-5
pii: 10.1007/s00595-020-01998-5
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
Programmed Cell Death 1 Receptor
0
pembrolizumab
DPT0O3T46P
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM