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FDA顾问委员会支持Grail公司的多癌症早期检测血液检测项目FDA顾问委员会支持Grail公司的多癌症早期检测血液检测项目

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2026年9月23日星期三,FDA顾问委员会以7比2(1人弃权)的投票结果,支持Grail公司的Galleri血液检测,该检测可筛查50岁及以上健康成年人体内超过50种癌症的信号。

FDA Advisory Panel Endorses Grail's Multi-Cancer Early Detection Blood Test On Wednesday, September 23, 2026, an FDA advisory panel voted 7-2 (with one abstention) to endorse Grail Inc.'s Galleri blood test, which screens for signals of over 50 types of cancer in healthy adults aged 50 and older. While the panel acknowledged the test's potential to identify cancers without existing screenings, it warned that the test is not a replacement for routine screenings and lacks evidence of reducing cancer deaths. The FDA will make a final decision on approval in a few months, which could lead to increased availability through Medicare and private insurance coverage.

虽然委员会认可该检测识别现有筛查手段无法覆盖癌症的潜力,但也警告称,该检测不能替代常规筛查,且缺乏降低癌症死亡率的证据。

FDA Advisory Panel Endorses Grail's Multi-Cancer Early Detection Blood Test On Wednesday, September 23, 2026, an FDA advisory panel voted 7-2 (with one abstention) to endorse Grail Inc.'s Galleri blood test, which screens for signals of over 50 types of cancer in healthy adults aged 50 and older. While the panel acknowledged the test's potential to identify cancers without existing screenings, it warned that the test is not a replacement for routine screenings and lacks evidence of reducing cancer deaths. The FDA will make a final decision on approval in a few months, which could lead to increased availability through Medicare and private insurance coverage.

FDA将在几个月内做出最终批准决定,这可能使该检测通过Medicare和私人保险覆盖而更广泛地普及。

FDA Advisory Panel Endorses Grail's Multi-Cancer Early Detection Blood Test On Wednesday, September 23, 2026, an FDA advisory panel voted 7-2 (with one abstention) to endorse Grail Inc.'s Galleri blood test, which screens for signals of over 50 types of cancer in healthy adults aged 50 and older. While the panel acknowledged the test's potential to identify cancers without existing screenings, it warned that the test is not a replacement for routine screenings and lacks evidence of reducing cancer deaths. The FDA will make a final decision on approval in a few months, which could lead to increased availability through Medicare and private insurance coverage.