TY - JOUR
T1 - Clinical and Diagnostic Utility of Genomic Profiling for Digestive Cancers
T2 - Real-World Evidence from Japan
AU - Ishikawa, Marin
AU - Nakamura, Kohei
AU - Kawano, Ryutaro
AU - Hayashi, Hideyuki
AU - Ikeda, Tatsuru
AU - Saito, Makoto
AU - Niida, Yo
AU - Sasaki, Jiichiro
AU - Okuda, Hiroyuki
AU - Ishihara, Satoshi
AU - Yamaguchi, Masatoshi
AU - Shimada, Hideaki
AU - Isobe, Takeshi
AU - Yuza, Yuki
AU - Yoshimura, Akinobu
AU - Kuroda, Hajime
AU - Yukisawa, Seigo
AU - Aoki, Takuya
AU - Takeshita, Kei
AU - Ueno, Shinichi
AU - Nakazawa, Junichi
AU - Sunakawa, Yu
AU - Nohara, Sachio
AU - Okada, Chihiro
AU - Nishimiya, Ko
AU - Tanishima, Shigeki
AU - Nishihara, Hiroshi
N1 - Publisher Copyright:
© 2024 by the authors.
PY - 2024/4
Y1 - 2024/4
N2 - The usefulness of comprehensive genomic profiling (CGP) in the Japanese healthcare insurance system remains underexplored. Therefore, this large-scale study aimed to determine the usefulness of CGP in diagnosing digestive cancers. Patients with various cancer types recruited between March 2020 and October 2022 underwent the FoundationOne® CDx assay at the Keio PleSSision Group (19 hospitals in Japan). A scoring system was developed to identify potentially actionable genomic alterations of biological significance and actionable genomic alterations. The detection rates for potentially actionable genomic alterations, actionable genomic alterations, and alterations equivalent to companion diagnosis (CDx), as well as the signaling pathways associated with these alterations in each digestive cancer, were analyzed. Among the 1587 patients, 547 had digestive cancer. The detection rates of potentially actionable genomic alterations, actionable genomic alterations, and alterations equivalent to CDx were 99.5%, 62.5%, and 11.5%, respectively. APC, KRAS, and CDKN2A alterations were frequently observed in colorectal, pancreatic, and biliary cancers, respectively. Most digestive cancers, except esophageal cancer, were adenocarcinomas. Thus, the classification flowchart for digestive adenocarcinomas proposed in this study may facilitate precise diagnosis. CGP has clinical and diagnostic utility in digestive cancers.
AB - The usefulness of comprehensive genomic profiling (CGP) in the Japanese healthcare insurance system remains underexplored. Therefore, this large-scale study aimed to determine the usefulness of CGP in diagnosing digestive cancers. Patients with various cancer types recruited between March 2020 and October 2022 underwent the FoundationOne® CDx assay at the Keio PleSSision Group (19 hospitals in Japan). A scoring system was developed to identify potentially actionable genomic alterations of biological significance and actionable genomic alterations. The detection rates for potentially actionable genomic alterations, actionable genomic alterations, and alterations equivalent to companion diagnosis (CDx), as well as the signaling pathways associated with these alterations in each digestive cancer, were analyzed. Among the 1587 patients, 547 had digestive cancer. The detection rates of potentially actionable genomic alterations, actionable genomic alterations, and alterations equivalent to CDx were 99.5%, 62.5%, and 11.5%, respectively. APC, KRAS, and CDKN2A alterations were frequently observed in colorectal, pancreatic, and biliary cancers, respectively. Most digestive cancers, except esophageal cancer, were adenocarcinomas. Thus, the classification flowchart for digestive adenocarcinomas proposed in this study may facilitate precise diagnosis. CGP has clinical and diagnostic utility in digestive cancers.
KW - adenocarcinoma
KW - cancer gene panel
KW - comprehensive genomic profiling
KW - pathological diagnosis
UR - https://www.scopus.com/pages/publications/85191582661
UR - https://www.scopus.com/pages/publications/85191582661#tab=citedBy
U2 - 10.3390/cancers16081504
DO - 10.3390/cancers16081504
M3 - Article
AN - SCOPUS:85191582661
SN - 2072-6694
VL - 16
JO - Cancers
JF - Cancers
IS - 8
M1 - 1504
ER -