Gene therapy has given sickle cell disease what medicine has long promised but rarely delivered: the possibility of a cure. Yet the slow uptake of Casgevy and Lyfgenia shows that even dazzling science can falter when it collides with cost, logistics, risks, and a medical system many patients distrust.
In December 2023, the FDA approved the first two gene therapies with curative potential for sickle cell disease (SCD): Casgevy, which uses CRISPR to edit a patient’s own stem cells, and Lyfgenia, which uses a viral vector to deliver a functional gene. For a disease as painful and disabling as sickle cell disease, one might have expected a rush toward treatment. Yet unlike the rapid public embrace of GLP-1 drugs, that rush has not materialized. Last year, only 64 patients received Casgevy, and about 100 received Lyfgenia. In the United States, more than 100,000 people live with sickle cell disease.
Sickle Cell, Gene Therapy, and the Limits of Medical Triumph
Source
AMERICAN COUNCIL ON SCIENCE AND HEALTH
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