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Clinical utility of comprehensive genomic profiling tests for advanced or metastatic solid tumor in clinical practice

Authors :
Hanae Ida
Takafumi Koyama
Takaaki Mizuno
Kuniko Sunami
Takashi Kubo
Kazuki Sudo
Kayoko Tao
Makoto Hirata
Kan Yonemori
Ken Kato
Takuji Okusaka
Yuichiro Ohe
Yoshiyuki Matsui
Naoya Yamazaki
Chitose Ogawa
Akira Kawai
Yoshitaka Narita
Minoru Esaki
Noboru Yamamoto
Source :
Cancer Science. 113:4300-4310
Publication Year :
2022
Publisher :
Wiley, 2022.

Abstract

Previous clinical trials indicate that 10%-25% of patients received genomically matched therapy after comprehensive genomic profiling (CGP) tests. However, the clinical utility of CGP tests has not been assessed in clinical practice. We assessed the clinical utility of CGP tests for advanced or metastatic solid tumor and determined the proportion of patients receiving genomically matched therapy among those with common and non-common cancers. From August 2019 to July 2020, a total of 418 patients had undergone CGP tests, and the results were discussed through the molecular tumor board at our site. The median age of patients was 57 (range: 3-86) years. Colorectal cancer was the most common, with 47 (11%) patients. Actionable genomic alterations (median 3, range: 1-17) were identified in 368 (88.0%) of 418 patients. Druggable genomic alterations were determined in 196 (46.9%) of 418 patients through the molecular tumor board. Genomically matched therapy was administered as the subsequent line of therapy in 51 (12.2%) patients, which is comparable to the proportion we previously reported in a clinical trial (13.4%) (p = 0.6919). The proportion of patients receiving genomically matched therapy was significantly higher among those with common cancers (16.2%) than non-common cancers (9.4%) (p = 0.0365). Genomically matched therapy after the CGP tests was administered to 12.2% of patients, which is similar to the proportion reported in the previous clinical trials. The clinical utility of CGP tests in patients with common cancers greatly exceeded that in patients with non-common cancers.

Details

ISSN :
13497006 and 13479032
Volume :
113
Database :
OpenAIRE
Journal :
Cancer Science
Accession number :
edsair.doi.dedup.....3ddd4175d169ea9cb6b1821d65644cd1
Full Text :
https://doi.org/10.1111/cas.15586