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Patient-reported outcomes in ZUMA-7, a phase 3 study of axicabtagene ciloleucel in second-line large B-cell lymphoma.
Elsawy, Mahmoud; Chavez, Julio C; Avivi, Irit; Larouche, Jean-François; Wannesson, Luciano; Cwynarski, Kate; Osman, Keren; Davison, Kelly; Rudzki, Jakob D; Dahiya, Saurabh; Dorritie, Kathleen; Jaglowski, Samantha; Radford, John; Morschhauser, Franck; Cunningham, David; Martin Garcia-Sancho, Alejandro; Tzachanis, Dimitrios; Ulrickson, Matthew L; Karmali, Reem; Kekre, Natasha; Thieblemont, Catherine; Enblad, Gunilla; Dreger, Peter; Malladi, Ram; Joshi, Namita; Wang, Wei-Jhih; Solem, Caitlyn T; Snider, Julia Thornton; Cheng, Paul; To, Christina; Kersten, Marie José.
Afiliação
  • Elsawy M; Queen Elizabeth II Health Sciences Centre and Division of Hematology, Department of Medicine, Dalhousie University, Halifax, NS, Canada.
  • Chavez JC; Moffitt Cancer Center, Tampa, FL.
  • Avivi I; Hematology Institute, Tel Aviv Sourasky Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Larouche JF; Centre Hospitalier Universitaire (CHU) de Québec, Hôpital de l'Enfant-Jésus, Québec, QC, Canada.
  • Wannesson L; Istituto Oncologico della Svizzera Italiana, Bellinzona, Switzerland.
  • Cwynarski K; Department of Haematology, University College London Hospitals National Health Services (NHS) Foundation Trust, London, United Kingdom.
  • Osman K; Icahn School of Medicine at Mount Sinai, New York, NY.
  • Davison K; Royal Victoria Hospital, McGill University Health Centre, Montreal, QC, Canada.
  • Rudzki JD; Department of Hematology & Oncology, The Medical University of Innsbruck, University Clinic for Internal Medicine, Innsbruck, Austria.
  • Dahiya S; Greenebaum Comprehensive Cancer Center, Transplant and Cellular Therapy Program, University of Maryland Medical Center, Baltimore, MD.
  • Dorritie K; University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center, Pittsburgh, PA.
  • Jaglowski S; Comprehensive Cancer Center, Blood and Marrow Transplant Program, The Ohio State University, Columbus, OH.
  • Radford J; Division of Cancer Sciences, The Christie NHS Foundation Trust and the University of Manchester, Manchester, United Kingdom.
  • Morschhauser F; Groupe de Recherche sur les formes Injectables et les Technologies Associées, University of Lille, CHU Lille, Lille, France.
  • Cunningham D; The Royal Marsden NHS Foundation Trust, London, United Kingdom.
  • Martin Garcia-Sancho A; Hematology Department, Salamanca University Hospital, Institute of Biomedical Research of Salamanca (IBSAL), Centro de Investigación Biomédica en Red Cáncer (CIBERONC), Salamanca, Spain.
  • Tzachanis D; Moores Cancer Center, University of California, San Diego, La Jolla, CA.
  • Ulrickson ML; Banner MD Anderson Cancer Center, Gilbert, AZ.
  • Karmali R; Division of Hematology and Oncology, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL.
  • Kekre N; The Ottawa Hospital, Ottawa, ON, Canada.
  • Thieblemont C; University of Paris, Hôpital Saint-Louis, Hemato-Oncology, DMU DHI, Paris, France.
  • Enblad G; Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
  • Dreger P; Department of Medicine, University of Heidelberg, Heidelberg, Germany.
  • Malladi R; Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Joshi N; University Hospitals Birmingham NHS Foundation Trust, Cambridge, United Kingdom.
  • Wang WJ; OPEN Health, Bethesda, MD.
  • Solem CT; OPEN Health, Bethesda, MD.
  • Snider JT; OPEN Health, Bethesda, MD.
  • Cheng P; Kite, a Gilead Company, Santa Monica, CA.
  • To C; Kite, a Gilead Company, Santa Monica, CA.
  • Kersten MJ; Kite, a Gilead Company, Santa Monica, CA.
Blood ; 140(21): 2248-2260, 2022 11 24.
Article em En | MEDLINE | ID: mdl-35839452
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Linfoma Difuso de Grandes Células B Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Linfoma Difuso de Grandes Células B Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article