Year: 2017
Type: article
Abstract: The US Food and Drug Administration’s (FDA’s) recent approval of Kymriah (tisagenlecleucel) for the treatment of acute lymphoblastic leukemia1 represents a triumph for the academic and pharmaceutical industry collaborators who enabled the success of this CD19 antigen-directed chimeric antigen receptor (CAR) T cell product. The stunning complete response rate in otherwise refractory disease has rightly attracted enormous attention and comment,2 which will not be added to here. Of almost equal importance, however, is that approval is focusing attention on the new resources and policies required if the success of CD19 CAR T cell treatment of B cell malignancies is to be more broadly replicated.
Source: Molecular Therapy
Author: Malcolm K. Brenner
Language: English
Topic: CAR-T cell therapy research
Subfield: Oncology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
OpenAlex ID: W2754432318
