Chimeric antigen receptor T-cell (CAR-T) therapies have been a welcome addition to the treatment paradigm for patients with relapsed and refractory multiple myeloma and large B-cell lymphoma (LBCL) who have gone through several prior rounds of treatment and run out of good options. But within the next few months CAR-T therapies may take their first steps into earlier lines of treatment, raising the question of how physicians will adapt to use of these complex and costly treatments in new settings.
Gilead Sciences, Inc. is slated to get a decision from the US Food and Drug Administration by 1 April regarding its supplemental biologics license application (sBLA) for Yescarta (axicabtagene ciloleucel) in the second-line treatment of LBCL