The treatment, known as axicabtagene ciloleucel, is made by adding a gene for a special receptor called chimeric antigen receptor (CAR) to the patient's T cells, multiplying them and infusing them into the patient. The cells then target the CD19 protein found on most B-cell lymphoma cells.
In the phase 3 test with 359 volunteers who had relapsed within 12 months after first-line chemoimmunotherapy, those given the CAR T treatment, also known as axi-cel, had a median event-free survival of 8.3 months versus 2.0 months among the patients who received two or three more cycles of chemoimmunotherapy followed by high-dose chemo with autologous stem-cell transplant.
The 24-month event-free survival rates were 41% and 16% respectively (P<0.001).
Estimated 2-year survival was 61% with axi-cel verus 52% with standard care.
Adverse events rated grade 3 or higher appeared in 83% of patients undergoing standard care, and that rate bumped up to 91% with axi-cel therapy.
Neurologic events of grade 3 or higher were seen in 21% of axi-cel recipients. Cytokine release syndrome of grade 3 or higher occurred in 6% of CAR T patients.
Kite, a Gilead Company, released topline results of the ZUMA-7 study June 28.
SOURCE: https://bit.ly/31BB6kh The New England Journal of Medicine, online December 11, 2021.
By Gene Emery
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