Health-related quality of life in patients with newly diagnosed multiple myeloma ineligible for stem cell transplantation: results from the randomized phase III ALCYONE trial
-
Published:2021-06-02
Issue:1
Volume:21
Page:
-
ISSN:1471-2407
-
Container-title:BMC Cancer
-
language:en
-
Short-container-title:BMC Cancer
Author:
Knop StefanORCID, Mateos Maria-Victoria, Dimopoulos Meletios A., Suzuki Kenshi, Jakubowiak Andrzej, Doyen Chantal, Lucio Paulo, Nagy Zsolt, Usenko Ganna, Pour Ludek, Cook Mark, Grosicki Sebastian, Crepaldi Andre, Liberati Anna Marina, Campbell Philip, Shelekhova Tatiana, Yoon Sung-Soo, Losava Genadi, Fujisaki Tomoaki, Garg Mamta, Wang Jianping, Wroblewski Susan, Kudva Anupa, Gries Katharine S., Fastenau John, San-Miguel Jesus, Cavo Michele
Abstract
Abstract
Background
In the phase III ALCYONE trial, daratumumab plus bortezomib/melphalan/prednisone (D-VMP) significantly improved overall response rate and progression-free status compared with VMP alone in transplant-ineligible patients with newly diagnosed multiple myeloma (NDMM). Here, we present patient-reported outcomes (PROs) from ALCYONE.
Methods
The European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30-item (EORTC QLQ-C30) and EuroQol 5-dimensional descriptive system (EQ-5D-5L) questionnaire were administered at baseline, every 3 months (year 1) and every 6 months (until progression). Treatment effects were assessed using a repeated-measures, mixed-effects model.
Results
Compliance with PRO assessments was comparable at baseline (> 90%) and throughout study (> 76%) for both treatment groups. Improvements from baseline were observed in both groups for EORTC QLQ-C30 Global Health Status (GHS), most functional scales, symptom scales and EQ-5D-5L visual analog scale (VAS). Between-group differences were significant for GHS (p = 0.0240) and VAS (p = 0.0160) at month 3. Improvements in pain were clinically meaningful in both groups at all assessment time points. Cognitive function declined in both groups, but the magnitude of the decline was not clinically meaningful.
Conclusions
Patients with transplant-ineligible NDMM demonstrated early and continuous improvements in health-related quality of life, including improvements in functioning and symptoms, following treatment with D-VMP or VMP.
Trial registration
ClinicalTrials.gov identifier NCT02195479, registered September 21, 2014
Funder
Janssen Pharmaceuticals
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics,Oncology
Reference34 articles.
1. Moreau P, San Miguel J, Sonneveld P, Mateos MV, Zamagni E, Avet-Loiseau H, et al. Multiple myeloma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2017;28(suppl 4):iv52–61. 2. Szabo K, Bodoki L, Nagy-Vincze M, Vincze A, Zilahi E, Szodoray P, et al. Effect of genetic and laboratory findings on clinical course of Antisynthetase syndrome in a Hungarian cohort. Biomed Res Int. 2018;2018:6416378. 3. Rodriguez-Otero P, Mateos MV, Martinez-Lopez J, Hernandez MT, Ocio EM, Rosinol L, et al. Predicting long-term disease control in transplant-ineligible patients with multiple myeloma: impact of an MGUS-like signature. Blood Cancer J. 2019;9(4):36. https://doi.org/10.1038/s41408-019-0176-x. 4. Moreau P, Attal M, Facon T. Frontline therapy of multiple myeloma. Blood. 2015;125(20):3076–84. https://doi.org/10.1182/blood-2014-09-568915. 5. Gandolfi S, Vekstein C, Laubach JP, O'Brien A, Masone K, Munshi NC, et al. The evolving role of transplantation in multiple myeloma: the need for a heterogeneous approach to a heterogeneous disease. Clin Adv Hematol Oncol. 2018;16(8):564–74.
Cited by
15 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|