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Targeted therapy guided by circulating tumor DNA analysis in advanced gastrointestinal tumors.
Nakamura, Yoshiaki; Ozaki, Hiroshi; Ueno, Makoto; Komatsu, Yoshito; Yuki, Satoshi; Esaki, Taito; Taniguchi, Hiroya; Sunakawa, Yu; Yamaguchi, Kensei; Kato, Ken; Denda, Tadamichi; Nishina, Tomohiro; Takahashi, Naoki; Satoh, Taroh; Yasui, Hisateru; Satake, Hironaga; Oki, Eiji; Kato, Takeshi; Ohta, Takashi; Matsuhashi, Nobuhisa; Goto, Masahiro; Okano, Naohiro; Ohtsubo, Koushiro; Yamazaki, Kentaro; Yamashita, Riu; Iida, Naoko; Yuasa, Mihoko; Bando, Hideaki; Yoshino, Takayuki.
Afiliação
  • Nakamura Y; International Research Promotion Office, National Cancer Center Hospital East, Kashiwa, Japan.
  • Ozaki H; Translational Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.
  • Ueno M; Department of Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
  • Komatsu Y; Translational Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.
  • Yuki S; Department of Gastroenterology, Kanagawa Cancer Center, Yokohama, Japan.
  • Esaki T; Department of Cancer Center, Hokkaido University Hospital, Sapporo, Japan.
  • Taniguchi H; Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo, Japan.
  • Sunakawa Y; Department of Gastrointestinal and Medical Oncology, NHO Kyushu Cancer Center, Fukuoka, Japan.
  • Yamaguchi K; Department of Clinical Oncology, Aichi Cancer Center, Nagoya, Japan.
  • Kato K; Department of Clinical Oncology, St. Marianna University School of Medicine, Kawasaki, Japan.
  • Denda T; Department of Gastroenterological Chemotherapy, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Nishina T; Department of Head and Neck, Esophageal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Takahashi N; Division of Gastroenterology, Chiba Cancer Center, Chiba, Japan.
  • Satoh T; Gastrointestinal Medical Oncology, NHO Shikoku Cancer Center, Matsuyama, Japan.
  • Yasui H; Department of Gastroenterology, Saitama Cancer Center, Ina, Japan.
  • Satake H; Center for Cancer Genomics and Precision Medicine, Osaka University Hospital, Suita, Japan.
  • Oki E; Department of Medical Oncology, Kobe City Medical Center General Hospital, Kobe, Japan.
  • Kato T; Cancer Treatment Center, Kansai Medical University Hospital, Hirakata, Japan.
  • Ohta T; Department of Medical Oncology, Kochi Medical School, Nankoku, Japan.
  • Matsuhashi N; Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Goto M; Department of Surgery, NHO Osaka National Hospital, Osaka, Japan.
  • Okano N; Department of Clinical Oncology, Kansai Rosai Hospital, Amagasaki, Japan.
  • Ohtsubo K; Department of Gastroenterological Surgery and Pediatric Surgery, Center for One Medicine Innovative Translational Research (COMIT), Gifu University Graduate School of Medicine, Gifu, Japan.
  • Yamazaki K; Cancer Chemotherapy Center, Osaka Medical and Pharmaceutical University Hospital, Takatsuki, Japan.
  • Yamashita R; Department of Medical Oncology, Kyorin University Faculty of Medicine, Tokyo, Japan.
  • Iida N; Department of Medical Oncology, Kanazawa University Hospital, Kanazawa, Japan.
  • Yuasa M; Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Nagaizumi, Japan.
  • Bando H; Division of Translational Informatics, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa, Japan.
  • Yoshino T; Translational Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.
Nat Med ; 2024 Sep 16.
Article em En | MEDLINE | ID: mdl-39284955
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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article