TY - JOUR
T1 - Indirect treatment comparison of brexucabtagene autoleucel (ZUMA-2) versus standard of care (SCHOLAR-2) in relapsed/refractory mantle cell lymphoma
AU - Hess, Georg
AU - Dreyling, Martin
AU - Oberic, Lucie
AU - Gine, Eva
AU - Zinzani, Pier Luigi
AU - Linton, Kim
AU - Vilmar, Adam
AU - Jerkeman, Mats
AU - Chen, Jenny M.H.
AU - Ohler, Anke
AU - Stilgenbauer, Stephan
AU - Thieblemont, Catherine
AU - Lambert, Jonathan
AU - Zilioli, Vittorio Ruggero
AU - Sancho, Juan Manuel
AU - Jimenez-Ubieto, Ana
AU - Fischer, Luca
AU - Eyre, Toby A.
AU - Keeping, Sam
AU - Park, Julie E.
AU - Wu, James J.
AU - Nunes, Ana
AU - Reitan, John
AU - Wade, Sally W.
AU - Salles, Gilles
N1 - Publisher Copyright:
© 2023 Kite Pharma. Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2024
Y1 - 2024
N2 - The SCHOLAR-2 retrospective study highlighted poor overall survival (OS) with standard of care (SOC) regimens among patients with relapsed/refractory (R/R) mantle cell lymphoma (MCL) who failed a covalent Bruton tyrosine kinase inhibitor (BTKi). In the ZUMA-2 single-arm trial, brexucabtagene autoleucel (brexu-cel; autologous anti-CD19 CAR T-cell therapy) demonstrated high rates of durable responses in patients with R/R MCL who had previous BTKi exposure. Here, we compared OS in ZUMA-2 and SCHOLAR-2 using three different methods which adjusted for imbalances in prognostic factors between populations: inverse probability weighting (IPW), regression adjustment (RA), and doubly robust (DR). Brexu-cel was associated with improved OS compared to SOC across all unadjusted and adjusted comparisons. Hazard ratios (95% confidence intervals) were 0.38 (0.23, 0.61) for IPW, 0.45 (0.28, 0.74) for RA, and 0.37 (0.23, 0.59) for DR. These results suggest a substantial survival benefit with brexu-cel versus SOC in patients with R/R MCL after BTKi exposure.
AB - The SCHOLAR-2 retrospective study highlighted poor overall survival (OS) with standard of care (SOC) regimens among patients with relapsed/refractory (R/R) mantle cell lymphoma (MCL) who failed a covalent Bruton tyrosine kinase inhibitor (BTKi). In the ZUMA-2 single-arm trial, brexucabtagene autoleucel (brexu-cel; autologous anti-CD19 CAR T-cell therapy) demonstrated high rates of durable responses in patients with R/R MCL who had previous BTKi exposure. Here, we compared OS in ZUMA-2 and SCHOLAR-2 using three different methods which adjusted for imbalances in prognostic factors between populations: inverse probability weighting (IPW), regression adjustment (RA), and doubly robust (DR). Brexu-cel was associated with improved OS compared to SOC across all unadjusted and adjusted comparisons. Hazard ratios (95% confidence intervals) were 0.38 (0.23, 0.61) for IPW, 0.45 (0.28, 0.74) for RA, and 0.37 (0.23, 0.59) for DR. These results suggest a substantial survival benefit with brexu-cel versus SOC in patients with R/R MCL after BTKi exposure.
KW - brexucabtagene autoleucel
KW - CAR T-cell therapy
KW - indirect treatment comparison
KW - mantle cell lymphoma
KW - non-Hodgkin lymphoma
KW - standard of care
U2 - 10.1080/10428194.2023.2268228
DO - 10.1080/10428194.2023.2268228
M3 - Article
C2 - 37840282
AN - SCOPUS:85174242231
SN - 1042-8194
VL - 65
SP - 14
EP - 25
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 1
ER -