Efficacy and toxicity management of 19-28z CAR T cell therapy in B cell acute lymphoblastic leukemia

ML Davila, I Riviere, X Wang, S Bartido, J Park… - Science translational …, 2014 - science.org
ML Davila, I Riviere, X Wang, S Bartido, J Park, K Curran, SS Chung, J Stefanski…
Science translational medicine, 2014science.org
We report on 16 patients with relapsed or refractory B cell acute lymphoblastic leukemia (B-
ALL) that we treated with autologous T cells expressing the 19-28z chimeric antigen
receptor (CAR) specific to the CD19 antigen. The overall complete response rate was 88%,
which allowed us to transition most of these patients to a standard-of-care allogeneic
hematopoietic stem cell transplant (allo-SCT). This therapy was as effective in high-risk
patients with Philadelphia chromosome–positive (Ph+) disease as in those with relapsed …
We report on 16 patients with relapsed or refractory B cell acute lymphoblastic leukemia (B-ALL) that we treated with autologous T cells expressing the 19-28z chimeric antigen receptor (CAR) specific to the CD19 antigen. The overall complete response rate was 88%, which allowed us to transition most of these patients to a standard-of-care allogeneic hematopoietic stem cell transplant (allo-SCT). This therapy was as effective in high-risk patients with Philadelphia chromosome–positive (Ph+) disease as in those with relapsed disease after previous allo-SCT. Through systematic analysis of clinical data and serum cytokine levels over the first 21 days after T cell infusion, we have defined diagnostic criteria for a severe cytokine release syndrome (sCRS), with the goal of better identifying the subset of patients who will likely require therapeutic intervention with corticosteroids or interleukin-6 receptor blockade to curb the sCRS. Additionally, we found that serum C-reactive protein, a readily available laboratory study, can serve as a reliable indicator for the severity of the CRS. Together, our data provide strong support for conducting a multicenter phase 2 study to further evaluate 19-28z CAR T cells in B-ALL and a road map for patient management at centers now contemplating the use of CAR T cell therapy.
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