Real-world data on microsatellite instability status in various unresectable or metastatic solid tumors.


Journal

Cancer science
ISSN: 1349-7006
Titre abrégé: Cancer Sci
Pays: England
ID NLM: 101168776

Informations de publication

Date de publication:
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

1105-1113

Subventions

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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Auteurs

Kiwamu Akagi (K)

Department of Molecular Diagnosis and Cancer Prevention, Saitama Cancer Center, Saitama, Japan.

Eiji Oki (E)

Department of Surgery and Science, Graduate School of Medical Science, Kyushu University, Fukuoka, Japan.

Hiroya Taniguchi (H)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Kaname Nakatani (K)

Department of Molecular and Laboratory Medicine, Mie University Graduate School of Medicine, Tsu, Japan.

Daisuke Aoki (D)

Department of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.

Takeshi Kuwata (T)

Department of Genetic Medicine and Services, National Cancer Center Hospital East, Kashiwa, Japan.

Takayuki Yoshino (T)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

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Classifications MeSH