Real-world data on microsatellite instability status in various unresectable or metastatic solid tumors.
Adolescent
Adult
Age Factors
Aged
Aged, 80 and over
Antibodies, Monoclonal, Humanized
Child
Child, Preschool
Cohort Studies
DNA Mismatch Repair
Drug Resistance, Neoplasm
/ genetics
Female
Humans
Immune Checkpoint Inhibitors
/ pharmacology
Male
Microsatellite Instability
Middle Aged
Neoplasms
/ drug therapy
Programmed Cell Death 1 Receptor
/ antagonists & inhibitors
Risk Factors
Sex Factors
Young Adult
PD-1 blockade
advanced solid tumor
immune checkpoint inhibitor
microsatellite instability
mismatch repair
Journal
Cancer science
ISSN: 1349-7006
Titre abrégé: Cancer Sci
Pays: England
ID NLM: 101168776
Informations de publication
Date de publication:
Mar 2021
Mar 2021
Historique:
received:
21
09
2020
revised:
07
01
2021
accepted:
07
01
2021
pubmed:
7
1
2021
medline:
18
3
2021
entrez:
6
1
2021
Statut:
ppublish
Résumé
Microsatellite instability-high (MSI-H) is an important biomarker for predicting the effect of immune checkpoint inhibitors (ICIs) on advanced solid tumors. Microsatellite instability-high is detected in various cancers, but its frequency varies by cancer type and stage. Therefore, precise frequency is required to plan ICI therapy. In this study, the results of MSI tests actually carried out in clinical practice were investigated. In total, 26 469 samples of various cancers were examined between December 2018 and November 2019 to determine whether programmed cell death-1 blockade was indicated. The results of MSI tests were obtained for 26 237 (99.1%) of these samples. The male : female ratio was 51:49 and mean age was 64.3 years. In all samples, the overall frequency of MSI-H was 3.72%. By gender, the frequency of MSI-H was higher in female patients (4.75%) than in male patients (2.62%; P < .001). A comparison by age revealed that the frequency of MSI-H was significantly higher in patients younger than 40 years of age (6.12%) and 80 years or older (5.77%) than in patients aged between 60 and 79 years (3.09%; P < .001). Microsatellite instability-high was detected in 30 cancer types. Common cancer types were: endometrial cancer, 16.85%; small intestinal cancer, 8.63%; gastric cancer, 6.74%; duodenal cancer, 5.60%; and colorectal cancer, 3.78%. Microsatellite instability-high was detected in cancer derived from a wide variety of organs. The frequency of MSI-H varied by cancer type and onset age. These data should prove especially useful when considering ICI treatment.
Identifiants
pubmed: 33403729
doi: 10.1111/cas.14798
pmc: PMC7935787
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
Immune Checkpoint Inhibitors
0
PDCD1 protein, human
0
Programmed Cell Death 1 Receptor
0
pembrolizumab
DPT0O3T46P
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1105-1113Subventions
Organisme : Japan Society for the Promotion of Science
ID : JP18K07339
Organisme : National Cancer Center
ID : 31-A-2
Pays : Republic of Korea
Organisme : Japan Agency for Medical Research and Development
ID : JP18kk0205004
Organisme : Ono and Falco Biosystems
Organisme : Array Bio Pharma
Organisme : Daiichi Sankyo
Organisme : Dainippon Sumitomo Pharma
Organisme : MSD
Organisme : Novartis
Organisme : Ono
Organisme : Sysmex
Organisme : Takeda
Organisme : Chugai
Organisme : GSK
Organisme : Parexel
Organisme : Sanofi
Informations de copyright
© 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
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