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Health-related quality of life in patients with triple-class exposed relapsed and refractory multiple myeloma treated with idecabtagene vicleucel or standard regimens: patient-reported outcomes from the phase 3, randomised, open-label KarMMa-3 clinical trial

Title: Health-related quality of life in patients with triple-class exposed relapsed and refractory multiple myeloma treated with idecabtagene vicleucel or standard regimens: patient-reported outcomes from the phase 3, randomised, open-label KarMMa-3 clinical trial
Authors: Delforge M.; Patel K.; Eliason L.; Dhanda D.; Shi L.; Guo S.; Marshall T. S.; Arnulf B.; Cavo M.; Nooka A.; Manier S.; Callander N.; Giralt S.; Einsele H.; Ailawadhi S.; Popa McKiver M.; Cook M.; Rodriguez-Otero P.
Contributors: Delforge M.; Patel K.; Eliason L.; Dhanda D.; Shi L.; Guo S.; Marshall T.S.; Arnulf B.; Cavo M.; Nooka A.; Manier S.; Callander N.; Giralt S.; Einsele H.; Ailawadhi S.; Popa McKiver M.; Cook M.; Rodriguez-Otero P.
Publication Year: 2024
Collection: IRIS Università degli Studi di Bologna (CRIS - Current Research Information System)
Subject Terms: Health-related quality of life; triple-class exposed; relapsed; refractory; multiple myeloma; idecabtagene vicleucel; standard regimens; KarMMa-3 clinical trial
Description: Background: Chimeric antigen receptor T-cell therapy idecabtagene vicleucel (ide-cel) showed significantly improved progression-free survival compared with standard regimens in adults with relapsed and refractory multiple myeloma who had received two to four previous regimens in the ongoing phase 3 KarMMa-3 trial (NCT03651128). This study analysed patient-reported outcomes (PROs), a KarMMa-3 secondary endpoint. Methods: In the randomised, open-label, phase 3 KarMMa-3 trial, 386 patients in hospitals (≥18 years of age, with measurable disease and an Eastern Cooperative Oncology Group performance status score of 0 or 1, who had received two to four previous regimens—including an immunomodulatory agent, a proteasome inhibitor, and daratumumab—and had documented disease progression after receiving their last dose of the last therapy) were randomly assigned to ide-cel (n=254) or standard regimens (daratumumab, pomalidomide, and dexamethasone; daratumumab, bortezomib, and dexamethasone; ixazomib, lenalidomide, and dexamethasone; carfilzomib and dexamethasone; or elotuzumab, pomalidomide, and dexamethasone; n=132). Patients were expected to complete the European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life C30 Questionnaire (QLQ-C30), Multiple Myeloma Module (QLQ-MY20), EQ 5 dimensions (EQ-5D), and EQ-5D visual analogue scale (VAS) at baseline and follow-up timepoints (data cutoff April 18, 2022). PROs included nine prespecified primary domains: EORTC QLQ-C30 GHS–quality of life (QoL), physical functioning, cognitive functioning, fatigue, and pain; QLQ-MY20 disease symptoms and side effects of treatment; and five-level EQ-5D (EQ-5D-5L) index score and EQ-5D visual VAS. Differences in overall least-squares mean changes from baseline to month 20 were analysed using post-hoc constrained longitudinal data analysis. Time to confirmed improvement or deterioration from baseline was analysed using Cox proportional hazard models. Findings: Patients were randomly assigned between May 6, 2019, and ...
Document Type: article in journal/newspaper
File Description: ELETTRONICO
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/38423700; info:eu-repo/semantics/altIdentifier/wos/WOS:001200933500001; volume:11; issue:3; firstpage:216; lastpage:227; numberofpages:12; journal:THE LANCET. HAEMATOLOGY; https://hdl.handle.net/11585/969794
DOI: 10.1016/S2352-3026(24)00005-X
Availability: https://hdl.handle.net/11585/969794; https://doi.org/10.1016/S2352-3026(24)00005-X
Accession Number: edsbas.BBA02E9B
Database: BASE