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Assessment for the timing of comprehensive genomic profiling tests in patients with advanced solid cancers.
Hagio, Kanako; Kikuchi, Junko; Takada, Kohichi; Tanabe, Hiroki; Sugiyama, Minako; Ohhara, Yoshihito; Amano, Toraji; Yuki, Satoshi; Komatsu, Yoshito; Osawa, Takahiro; Hatanaka, Kanako C; Hatanaka, Yutaka; Mitamura, Takashi; Yabe, Ichiro; Matsuno, Yoshihiro; Manabe, Atsushi; Sakurai, Akihiro; Ishiguro, Atsushi; Takahashi, Masato; Yokouchi, Hiroshi; Naruse, Hirohito; Mizukami, Yusuke; Dosaka-Akita, Hirotoshi; Kinoshita, Ichiro.
Afiliação
  • Hagio K; Division of Clinical Cancer Genomics, Hokkaido University Hospital, Hokkaido, Japan.
  • Kikuchi J; Department of Breast Surgery, Hokkaido University Hospital, Hokkaido, Japan.
  • Takada K; Division of Clinical Cancer Genomics, Hokkaido University Hospital, Hokkaido, Japan.
  • Tanabe H; Department of Medical Oncology, Sapporo Medical University School of Medicine, Hokkaido, Japan.
  • Sugiyama M; Genetic Oncology Department, Asahikawa Medical University Hospital, Hokkaido, Japan.
  • Ohhara Y; Division of Clinical Cancer Genomics, Hokkaido University Hospital, Hokkaido, Japan.
  • Amano T; Department of Pediatrics, Hokkaido University Hospital, Hokkaido, Japan.
  • Yuki S; Division of Clinical Cancer Genomics, Hokkaido University Hospital, Hokkaido, Japan.
  • Komatsu Y; Department of Medical Oncology, Hokkaido University Hospital, Hokkaido, Japan.
  • Osawa T; Division of Clinical Cancer Genomics, Hokkaido University Hospital, Hokkaido, Japan.
  • Hatanaka KC; Department of Medical Oncology, Hokkaido University Hospital, Hokkaido, Japan.
  • Hatanaka Y; Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Hokkaido, Japan.
  • Mitamura T; Department of Cancer Chemotherapy, Hokkaido University Hospital, Cancer Center, Hokkaido, Japan.
  • Yabe I; Department of Renal and Genitourinary surgery, Hokkaido University Hospital, Hokkaido, Japan.
  • Matsuno Y; Center for Development of Advanced Diagnostics, Hokkaido University Hospital, Hokkaido, Japan.
  • Manabe A; Center for Development of Advanced Diagnostics, Hokkaido University Hospital, Hokkaido, Japan.
  • Sakurai A; Division of Clinical Genetics, Hokkaido University Hospital, Hokkaido, Japan.
  • Ishiguro A; Division of Clinical Genetics, Hokkaido University Hospital, Hokkaido, Japan.
  • Takahashi M; Department of Surgical Pathology, Hokkaido University Hospital, Hokkaido, Japan.
  • Yokouchi H; Department of Pediatrics, Hokkaido University Hospital, Hokkaido, Japan.
  • Naruse H; Department of Medical Genetics and Genomics, Sapporo Medical University, Hokkaido, Japan.
  • Mizukami Y; Department of Medical Oncology, Teine Keijinkai Hospital, Hokkaido, Japan.
  • Dosaka-Akita H; Department of Breast Surgery, Hokkaido University Hospital, Hokkaido, Japan.
  • Kinoshita I; Center for Clinical Cancer Genomics and Precision Medicine, NHO Hokkaido Cancer Center, Hokkaido, Japan.
Cancer Sci ; 114(8): 3385-3395, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37208840
Comprehensive genomic profiling (CGP) tests have been covered by public insurance in Japan for patients with advanced solid tumors who have completed or are completing standard treatments or do not have them. Therefore, genotype-matched drug candidates are often unapproved or off-label, and improving clinical trial access is critical, involving the appropriate timing of CGP tests. To address this issue, we analyzed the previous treatment data for 441 patients from an observational study on CGP tests discussed by the expert panel at Hokkaido University Hospital between August 2019 and May 2021. The median number of previous treatment lines was two; three or more lines accounted for 49%. Information on genotype-matched therapies was provided to 277 (63%). Genotype-matched clinical trials were ineligible because of an excess number of previous treatment lines or use of specific agents were found in 66 (15%) patients, with the highest proportion in breast and prostate cancers. Many patients met the exclusion criteria of one to two or more treatment lines across cancer types. In addition, previous use of specific agents was a frequent exclusion criterion for breast, prostate, colorectal, and ovarian cancers. The patients with tumor types with a low median number (two or fewer) of previous treatment lines, including most rare cancers, primary unknown cancers, and pancreatic cancers, had significantly fewer ineligible clinical trials. The earlier timing of CGP tests may improve access to genotype-matched clinical trials, with their proportion varying by cancer type. Each relevant society needs to advocate the desirable timing of CGP testing nationwide.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias Pancreáticas / Neoplasias da Próstata Tipo de estudo: Observational_studies Limite: Female / Humans / Male Idioma: En Revista: Cancer Sci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias Pancreáticas / Neoplasias da Próstata Tipo de estudo: Observational_studies Limite: Female / Humans / Male Idioma: En Revista: Cancer Sci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão