TY - JOUR
T1 - Real-world data on microsatellite instability status in various unresectable or metastatic solid tumors
AU - Akagi, Kiwamu
AU - Oki, Eiji
AU - Taniguchi, Hiroya
AU - Nakatani, Kaname
AU - Aoki, Daisuke
AU - Kuwata, Takeshi
AU - Yoshino, Takayuki
N1 - Funding Information:
K. Akagi reports research funding received from Ono and Falco Biosystems and lecture fees received from MSD. E. Oki reports lecture fees received from Bayer, Chugai, Eli Lilly, Merck, Ono, Taiho, Takeda, and Yakult Honsha. H. Taniguchi reports honoraria received from Bayer, Bristol‐Myers Squibb, Chugai, Daiichi Sankyo, Eli Lilly, MBL, Merck Serono, Mitsubishi Tanabe Pharma, MSD, Nippon Kayaku, Novartis, Sanofi, Taiho, Takeda, and Yakult Honsha and research funding received from Array Bio Pharma, Daiichi Sankyo, Dainippon Sumitomo Pharma, MSD, Novartis, Ono, Sysmex, and Takeda. D. Aoki reports research funding received from Chugai and Takada and honoraria received from Astra Zeneka, Chugai, and MSD. T. Kuwata reports research funding from Ono and Daiichi Sankyo and honoraria from MSD, Astra Zeneca, and Taiho. T. Yoshino reports research funding received from Chugai, Daiichi Sankyo, Dainippon Sumitomo Pharma, GSK, MSD, Novartis, Ono, Parexel, and Sanofi. The other authors have no conflicts of interest.
Funding Information:
We thank SRL Inc. for providing anonymized MSI data. This research was supported by the Japan Agency for Medical Research and Development (AMED) under grant JP18kk0205004, JSPS KAKENHI Grant Number JP18K07339, and National Cancer Center Research and Development Fund Grant Number 31‐A‐2.
Funding Information:
Japan Agency for Medical Research and Development (AMED), Grant/Award Number: JP18kk0205004; JSPS KAKENHI, Grant/Award Number: JP18K07339; National Cancer Center Research and Development Fund, Grant/Award Number: 31-A-2. We thank SRL Inc. for providing anonymized MSI data. This research was supported by the Japan Agency for Medical Research and Development (AMED) under grant JP18kk0205004, JSPS KAKENHI Grant Number JP18K07339, and National Cancer Center Research and Development Fund Grant Number 31-A-2.
Publisher Copyright:
© 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
PY - 2021/3
Y1 - 2021/3
N2 - 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.
AB - 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.
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U2 - 10.1111/cas.14798
DO - 10.1111/cas.14798
M3 - Article
C2 - 33403729
AN - SCOPUS:85100522315
SN - 1347-9032
VL - 112
SP - 1105
EP - 1113
JO - Cancer Science
JF - Cancer Science
IS - 3
ER -