Targeted therapy guided by circulating tumor DNA analysis in advanced gastrointestinal tumors

Yoshiaki Nakamura(National Cancer Center Hospital East), Hiroshi Ozaki(National Cancer Center Hospital East), Makoto Ueno(Kanagawa Prefectural Hospital Organization), Yoshito Komatsu(Hokkaido University Hospital), Satoshi Yuki(Hokkaido University Hospital), Taito Esaki(National Hospital Organization Kyushu Cancer Center), Hiroya Taniguchi(Aichi Cancer Center), Yu Sunakawa(St. Marianna University School of Medicine), Kensei Yamaguchi(Japanese Foundation For Cancer Research), Ken Kato(National Cancer Center Hospital East), Tadamichi Denda(Chiba Cancer Center), Tomohiro Nishina(Shikoku Cancer Center), Naoki Takahashi(Saitama Cancer Center), Taroh Satoh(Osaka University Hospital), Hisateru Yasui(Kobe City Medical Center General Hospital), Hironaga Satake(Kansai Medical University), Eiji Oki(Kyushu University), Takeshi Kato(Osaka National Hospital), Takashi Ohta(Kansai Rosai Hospital), Nobuhisa Matsuhashi(Gifu University), Masahiro Goto(Osaka University of Pharmaceutical Sciences), Naohiro Okano(Kyorin University), Koushiro Ohtsubo(Kanazawa University Hospital), Kentaro Yamazaki(Shizuoka Cancer Center), Riu Yamashita(National Cancer Center Hospital East), Naoko Iida(National Cancer Center Hospital East), Mihoko Yuasa(National Cancer Center Hospital East), Hideaki Bando(National Cancer Center Hospital East), Takayuki Yoshino(National Cancer Center Hospital East)
Nature Medicine
September 16, 2024
Cited by 47Open Access
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Abstract

Although comprehensive genomic profiling has become standard in oncology for advanced solid tumors, the full potential of circulating tumor DNA (ctDNA)-based profiling in capturing tumor heterogeneity and guiding therapy selection remains underexploited, marked by a scarcity of evidence on its clinical impact and the assessment of intratumoral heterogeneity. The GOZILA study, a nationwide, prospective observational ctDNA profiling study, previously demonstrated higher clinical trial enrollment rates using liquid biopsy compared with tissue screening. This updated analysis of 4,037 patients further delineates the clinical utility of ctDNA profiling in advanced solid tumors, showcasing a significant enhancement in patient outcomes with a 24% match rate for targeted therapy. Patients treated with matched targeted therapy based on ctDNA profiling demonstrated significantly improved overall survival compared with those receiving unmatched therapy (hazard ratio, 0.54). Notably, biomarker clonality and adjusted plasma copy number were identified as predictors of therapeutic efficacy, reinforcing the value of ctDNA in reflecting tumor heterogeneity for precise treatment decisions. These new insights into the relationship between ctDNA characteristics and treatment outcomes advance our understanding beyond the initial enrollment benefits. Our findings advocate for the broader adoption of ctDNA-guided treatment, signifying an advancement in precision oncology and improving survival outcomes in advanced solid tumors.


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