Cancer Discov. 2018 Dec;8(12):OF6. doi: 10.1158/2159-8290.CD-NB2018-136. Epub 2018 Oct 16.
The FDA granted marketing authorization to the first-ever next-generation sequencing assay for detecting minimal residual disease in patients with acute lymphoblastic leukemia or multiple myeloma.
美国食品药品监督管理局(FDA)批准了首个用于检测急性淋巴细胞白血病或多发性骨髓瘤患者微小残留病的新一代测序检测方法的上市许可。