Current Status of Comprehensive Genomic Profiling (CGP) in Miyazaki Prefecture and Review of the Literature

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Title ( eng )
Current Status of Comprehensive Genomic Profiling (CGP) in Miyazaki Prefecture and Review of the Literature
Creator
KAWANO Noriaki
KIKUCHI Ikuo
MARUTSUKA Kousuke
NISHIDA Takahiro
ARITA Shuji
YAMAJI Takumi
ITO Mamoru
YAMAGUCHI Kyoko
ISOBE Daichi
SHIMONODAN Hidemi
SHIMAKAWA Takashi
NAKAIKE Takashi
YAMASHITA Kiyoshi
HIMEJI Daisuke
MASHIBA Koichi
TANIGUCHI Shuichi
MATSUZAKI Sawako
MORI Yasuo
SEMBA Yuichiro
TAKIGAWA Ken
KATO Koji
MAEDA Takahiro
BABA Eishi
AKASHI Koichi
Source Title
Shimane Journal of Medical Science
Volume 42
Issue 3-4
Start Page 47
End Page 57
Journal Identifire
ISSN 03865959
EISSN 24332410
Descriptions
Abstract
Background: Comprehensive Genomic Profiling (CGP) testing has been covered by insurance in Japan since 2019. Miyazaki Prefectural Hospital began CGP in January 2024 after designation as a Cancer Genome Collaboration Hospital in 2023. Methods: A retrospective study was conducted on 24 CGP cases from January to December 2024 to assess current status and future challenges. Results: Median patient age was 60 years (range: 39–82), with female predominance (7 males, 17 females). All tests used tissue samples and the FoundationOne® CDx platform. CGP was conducted at first-line in 12% (rare/unknown primary), second-line in 46%, and third-line in 42%. Mean time from CGP submission to expert panel review was 32.1 days. Major tumor types were gastrointestinal (50%) and gynecologic (42%) cancers. DNA analysis was successful in all cases. The median number of actionable alterations was 5 (IQR: 1–9; range: 1–15). Common genomic alterations included TP53 and PIK3CA mutations. In addition, high tumor mutational burden (TMB high) was frequently observed as a biomarker feature. All 24 cases harbored at least one actionable mutation. Drug-accessible alterations were found in 62% (15/24), and 29% (7/24) received targeted treatments (treatment-matched rate), including pembrolizumab and capivasertib. Implementation rates varied by tumor type: 60% in gallbladder, 14% in uterine, and 33% in intrahepatic cholangiocarcinoma. Targeted therapy showed a trend toward prolonged survival without statistical significance. One case required genetic counseling for STK11 mutation. Conclusion: CGP has expanded opportunities to explore novel treatment strategies based on genomic alterations. It proved feasible and clinically valuable for identifying actionable mutations and guiding therapy. Future efforts should optimize timing, broaden access, and considenhance data to advance precision oncology.
Subjects
Comprehensive Genomic Profiling (CGP)
precision oncology
actionable genetic alterations
treatment-matched rate
overall survival
Language
eng
Resource Type departmental bulletin paper
Publisher
Faculty of Medicine, Shimane University
島根大学医学部
Date of Issued 2025-12
Rights
Faculty of Medicine, Shimane University
権利関係(リンク) Creative Commons License
This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Publish Type Version of Record
Access Rights open access
Relation
[NCID] AA00841586