Sasaki Taiga, Hiraki Hayato, Yashima-Abo Akiko, Nagashima Hiromi, Endo Fumitaka, Yaegashi Mizunori, Miura Shimpei, Obata Keiko, Yanagawa Naoki, Itamochi Hiroaki, Shirota Hidekazu, Iwaya Takeshi, Nishizuka Satoshi S
Division of Biomedical Research and Development, Iwate Medical University Institute for Biomedical Sciences, Yahaba, Japan.
Department of Respiratory Medicine, Iwate Medical University School of Medicine, Yahaba, Japan.
Cancer Sci. 2025 Mar;116(3):764-774. doi: 10.1111/cas.16446. Epub 2025 Jan 5.
In Japan, comprehensive genome profiling (CGP) as a companion diagnostic (CDx) has been covered by public insurance since June 2019, but the proportion of patients with cancer who actually received drug therapy based on CGP data is low. In the present study, we attempted to use CGP as a starting point for tumor-informed circulating tumor DNA (ctDNA) monitoring. We retrospectively validated 219 patients with malignant tumors who underwent CGP at Iwate Medical University Hospital between October 2019 and April 2023 in terms of patient demographics, genetic analysis, drug recommendations, and drug administration rate. The 219 cancer cases analyzed by CGP for 27 target organs, including prostate (n = 27, 12.3%), colorectal (n = 25, 11.4%), lung (n = 19, 8.7%), and other neoplasms (n = 148, 67.6%). Among the cohort, only 14 cases (6.4%) subsequently were able to undertake the recommended action by Molecular Tumor Board. Of patients who underwent ctDNA monitoring based on somatic mutations identified by CGP (n = 11), clinical validity was confirmed in terms of early relapse prediction (n = 5, 45.5%), treatment response evaluation (n = 10, 90.9%), and no relapse/regrowth corroboration (n = 2, 18.2%) whereas 90.9% (n = 10) of patients obtained information with at least one source of the clinical validity. Although the current rate of CGP contributing to a drug recommendation is low, CGP results can be an alternate resource for tumor-informed longitudinal ctDNA monitoring to provide information concerning early relapse prediction, treatment response evaluation, and no relapse/regrowth corroboration.
在日本,自2019年6月起,作为伴随诊断(CDx)的综合基因组分析(CGP)已被纳入公共保险范围,但基于CGP数据实际接受药物治疗的癌症患者比例较低。在本研究中,我们尝试将CGP作为肿瘤信息循环肿瘤DNA(ctDNA)监测的起点。我们回顾性验证了2019年10月至2023年4月期间在岩手医科大学医院接受CGP检测的219例恶性肿瘤患者的人口统计学、基因分析、药物推荐和药物给药率。通过CGP分析的219例癌症病例涉及27个靶器官,包括前列腺癌(n = 27,12.3%)、结直肠癌(n = 25,11.4%)、肺癌(n = 19,8.7%)和其他肿瘤(n = 148,67.6%)。在该队列中,只有14例(6.4%)随后能够按照分子肿瘤委员会的建议采取行动。在基于CGP鉴定的体细胞突变进行ctDNA监测的患者中(n = 11),在早期复发预测(n = 5,45.5%)、治疗反应评估(n = 10,90.9%)和无复发/再生长证实(n = 2,18.2%)方面证实了临床有效性,而90.9%(n = 10)的患者从至少一种临床有效性来源获得了信息。尽管目前CGP对药物推荐的贡献率较低,但CGP结果可作为肿瘤信息纵向ctDNA监测的替代资源,以提供有关早期复发预测、治疗反应评估和无复发/再生长证实的信息。