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

Author:

Elsawy Mahmoud1,Chavez Julio C.2,Avivi Irit3,Larouche Jean-François4,Wannesson Luciano5,Cwynarski Kate6,Osman Keren7,Davison Kelly8,Rudzki Jakob D.9,Dahiya Saurabh10,Dorritie Kathleen11ORCID,Jaglowski Samantha12ORCID,Radford John13ORCID,Morschhauser Franck14ORCID,Cunningham David15ORCID,Martin Garcia-Sancho Alejandro16ORCID,Tzachanis Dimitrios17ORCID,Ulrickson Matthew L.18,Karmali Reem19ORCID,Kekre Natasha20ORCID,Thieblemont Catherine21,Enblad Gunilla22,Dreger Peter23,Malladi Ram2425,Joshi Namita26,Wang Wei-Jhih26,Solem Caitlyn T.26ORCID,Snider Julia Thornton27ORCID,Cheng Paul27,To Christina27,Kersten Marie José28

Affiliation:

1. 1Queen Elizabeth II Health Sciences Centre and Division of Hematology, Department of Medicine, Dalhousie University, Halifax, NS, Canada

2. 2Moffitt Cancer Center, Tampa, FL

3. 3Hematology Institute, Tel Aviv Sourasky Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

4. 4Centre Hospitalier Universitaire (CHU) de Québec, Hôpital de l'Enfant-Jésus, Québec, QC, Canada

5. 5Istituto Oncologico della Svizzera Italiana, Bellinzona, Switzerland

6. 6Department of Haematology, University College London Hospitals National Health Services (NHS) Foundation Trust, London, United Kingdom

7. 7Icahn School of Medicine at Mount Sinai, New York, NY

8. 8Royal Victoria Hospital, McGill University Health Centre, Montreal, QC, Canada

9. 9Department of Hematology & Oncology, The Medical University of Innsbruck, University Clinic for Internal Medicine, Innsbruck, Austria

10. 10Greenebaum Comprehensive Cancer Center, Transplant and Cellular Therapy Program, University of Maryland Medical Center, Baltimore, MD

11. 11University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center, Pittsburgh, PA

12. 12Comprehensive Cancer Center, Blood and Marrow Transplant Program, The Ohio State University, Columbus, OH

13. 13Division of Cancer Sciences, The Christie NHS Foundation Trust and the University of Manchester, Manchester, United Kingdom

14. 14Groupe de Recherche sur les formes Injectables et les Technologies Associées, University of Lille, CHU Lille, Lille, France

15. 15The Royal Marsden NHS Foundation Trust, London, United Kingdom

16. 16Hematology Department, Salamanca University Hospital, Institute of Biomedical Research of Salamanca (IBSAL), Centro de Investigación Biomédica en Red Cáncer (CIBERONC), Salamanca, Spain

17. 17Moores Cancer Center, University of California, San Diego, La Jolla, CA

18. 18Banner MD Anderson Cancer Center, Gilbert, AZ

19. 19Division of Hematology and Oncology, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL

20. 20The Ottawa Hospital, Ottawa, ON, Canada

21. 21University of Paris, Hôpital Saint-Louis, Hemato-Oncology, DMU DHI, Paris, France

22. 22Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden

23. 23Department of Medicine, University of Heidelberg, Heidelberg, Germany

24. 24Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom

25. 25University Hospitals Birmingham NHS Foundation Trust, Cambridge, United Kingdom

26. 26OPEN Health, Bethesda, MD

27. 27Kite, a Gilead Company, Santa Monica, CA

28. 28Cancer Center Amsterdam, Department of Hematology, Amsterdam UMC on behalf of Stichting Hemato-Oncologie voor Volwassenen Nederland (HOVON)/ Lunenburg Lymphoma Phase 1 / II Consortium (LLPC), University of Amsterdam, Amsterdam, Netherlands

Abstract

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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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