Patient-reported outcomes in ZUMA-7, a phase 3 study of axicabtagene ciloleucel in second-line large B-cell lymphoma

Mahmoud Elsawy(Dalhousie University), Julio C. Chávez(Moffitt Cancer Center), Irit Avivi(Tel Aviv University), Jean-François Larouche(Hôpital de l'Enfant-Jésus), Luciano Wannesson(Università della Svizzera italiana), Kate Cwynarski(National Health Service), Keren Osman(Icahn School of Medicine at Mount Sinai), Kelly Davison(Royal Victoria Regional Health Centre), Jakob Rudzki(Innsbruck Medical University), Saurabh Dahiya(University of Maryland, Baltimore), Kathleen Dorritie(UPMC Hillman Cancer Center), Samantha Jaglowski(The Ohio State University), John Radford(University of Manchester), Franck Morschhauser(Université de Lille), David Cunningham(Royal Marsden NHS Foundation Trust), Alejandro Martı́n(Centro de Investigación Biomédica en Red), Dimitrios Tzachanis(University of California San Diego), Matthew L. Ulrickson(The University of Texas MD Anderson Cancer Center), Reem Karmali(Northwestern University), Natasha Kekre(Ottawa Hospital), Catherine Thiéblemont(Université Paris Cité), Gunilla Enblad(Uppsala University), Peter Dreger(Heidelberg University), Ram Malladi(University Hospitals Birmingham NHS Foundation Trust), Namita Joshi, Wei‐Jhih Wang, Caitlyn T. Solem, Julia Thornton Snider, Paul Cheng, Christina To, Marie José Kersten(Hovon)
Blood
July 15, 2022
Cited by 74Open Access
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Abstract

Here, we report the first comparative analysis of patient-reported outcomes (PROs) with chimeric antigen receptor T-cell therapy vs standard-of-care (SOC) therapy in second-line relapsed/refractory large B-cell lymphoma (R/R LBCL) from the pivotal randomized phase 3 ZUMA-7 study of axicabtagene ciloleucel (axi-cel) vs SOC. PRO instruments were administered at baseline, day 50, day 100, day 150, month 9, and every 3 months from randomization until 24 months or an event-free survival event. The quality of life (QoL) analysis set comprised patients with a baseline and ≥1 follow-up PRO completion. Prespecified hypotheses for Quality of Life Questionnaire-Core 30 (QLQ-C30) physical functioning, global health status/QoL, and EQ-5D-5L visual analog scale (VAS) were tested using mixed-effects models with repeated measures. Clinically meaningful changes were defined as 10 points for QLQ-C30 and 7 for EQ-5D-5L VAS. Among 359 patients, 296 (165 axi-cel, 131 SOC) met inclusion criteria for QoL analysis. At day 100, statistically significant and clinically meaningful differences in mean change of scores from baseline were observed favoring axi-cel over SOC for QLQ-C30 global health status/QoL (estimated difference 18.1 [95% confidence interval (CI), 12.3-23.9]), physical functioning (13.1 [95% CI, 8.0-18.2]), and EQ-5D-5L VAS (13.7 [95% CI, 8.5-18.8]; P < .0001 for all). At day 150, scores significantly favored axi-cel vs SOC for global health status/QoL (9.8 [95% CI, 2.6-17.0]; P = .0124) and EQ-5D-5L VAS (11.3 [95% CI, 5.4-17.1]; P = .0004). Axi-cel showed clinically meaningful improvements in QoL over SOC. Superior clinical outcomes and favorable patient experience with axi-cel should help inform treatment choices in second-line R/R LBCL. This trial was registered at www.clinicaltrials.gov as #NCT03391466.


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