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[癌症基因组医学中伴随诊断的现状与问题]

[Current Status and Issues of Companion Diagnostics in Cancer Genomic Medicine].

作者信息

Kanai Masashi

机构信息

Dept. of Therapeutic Oncology, Graduate School of Medicine, Kyoto University.

出版信息

Gan To Kagaku Ryoho. 2024 Apr;51(4):388-391.

Abstract

As of December 2023, there are 5 types of cancer gene panel tests covered by public insurance in Japan. Four of them partly feature companion diagnostics. When cancer gene panel test is used for the purpose of comprehensive gene profiling (CGP), a total of 56,000 points(44,000 points for the test administration fee and 12,000 points for the expert panel fee) can be claimed, whereas if the cancer gene panel test is used for the purpose of companion diagnostics, hospitals can claim only the reimbursement as a companion diagnostics, which fee is much cheaper than that of CGP. Therefore, cancer gene panel tests are rarely used as a companion diagnosis in daily clinical practice. Even when the test is performed as a CGP test, since its indication is limited to patients who have completed or are expected to complete standard chemotherapy, most biomarkers associated with approved drugs are already evaluated with stand-alone companion diagnostics at the time of CGP test application. On the other hand, there are some approved drugs, such as pembrolizumab for TMB-H or entrectinib or larotrectinib for NTRK fusion gene, for which there is no stand-alone companion diagnostics and the eligibility for these drugs cannot be judged without the results of CGP test. This paper discusses the current status and issues of companion diagnostics in cancer genomic medicine.

摘要

截至2023年12月,日本公共保险涵盖5种癌症基因检测套餐。其中4种部分具有伴随诊断功能。当癌症基因检测套餐用于全面基因谱分析(CGP)时,总共可报销56000分(检测管理费44000分,专家小组费12000分),而如果癌症基因检测套餐用于伴随诊断目的,医院只能报销作为伴随诊断的费用,该费用比CGP便宜得多。因此,癌症基因检测套餐在日常临床实践中很少用作伴随诊断。即使作为CGP检测进行,由于其适应症仅限于已完成或预计完成标准化疗的患者,在应用CGP检测时,大多数与获批药物相关的生物标志物已通过单独的伴随诊断进行评估。另一方面,有一些获批药物,如用于TMB-H的帕博利珠单抗或用于NTRK融合基因的恩曲替尼或拉罗替尼,没有单独的伴随诊断,没有CGP检测结果就无法判断这些药物的适用资格。本文讨论了癌症基因组医学中伴随诊断的现状和问题。

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