Health-related quality of life in the ENDEAVOR study: carfilzomib-dexamethasone vs bortezomib-dexamethasone in relapsed/refractory multiple myeloma.


Journal

Blood cancer journal
ISSN: 2044-5385
Titre abrégé: Blood Cancer J
Pays: United States
ID NLM: 101568469

Informations de publication

Date de publication:
22 02 2019
Historique:
received: 21 06 2018
accepted: 21 01 2019
revised: 14 01 2019
entrez: 24 2 2019
pubmed: 24 2 2019
medline: 3 1 2020
Statut: epublish

Résumé

We examined effects of carfilzomib-dexamethasone (Kd56) versus bortezomib-dexamethasone (Vd) on health-related quality of life (HR-QoL) in relapsed/refractory multiple myeloma (MM) patients from the ENDEAVOR study. HR-QoL was assessed by the European Organisation for Research and Treatment of Cancer QoL Questionnaire (QLQ-C30), MM-specific module (QLQ-MY20), and Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Neurotoxicity (FACT-GOG-Ntx) "Additional Concerns" neurotoxicity subscale. The QLQ-C30 Global Health Status (GHS)/QoL scale and seven prespecified subscales were compared between groups using mixed model for repeated measures. Of 929 randomized patients, 911 with ≥1 post-baseline assessment were included. Kd56 was associated with statistically significant improvements in GHS/QoL, fatigue, pain, side effects, and FACT/GOG-Ntx scores versus Vd, although mean differences did not meet thresholds for clinical significance. The Kd56 group had longer time to deterioration (TTD) in GHS/QoL (median 3.7 versus 2.8 months, p = 0.0046), physical function (5.6 versus 3.7 months, p = 0.0390), nausea/vomiting (17.6 versus 8.2 months, p = 0.0358), side effects (6.4 versus 3.7 months p < 0.0001), and FACT/GOG-Ntx (11.1 versus 5.5 months, p = 0.0004). Overall, Kd56 resulted in statistically but not clinically significant improvements in mean GHS/QoL scores versus Vd. Treatment with Kd56 versus Vd also significantly prolonged TTD in GHS/QoL, physical function, nausea/vomiting, side effects, and FACT/GOG-Ntx.

Identifiants

pubmed: 30796199
doi: 10.1038/s41408-019-0181-0
pii: 10.1038/s41408-019-0181-0
pmc: PMC6386751
doi:

Substances chimiques

Oligopeptides 0
Bortezomib 69G8BD63PP
carfilzomib 72X6E3J5AR
Dexamethasone 7S5I7G3JQL

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

23

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Auteurs

Heinz Ludwig (H)

Wilhelminen Cancer Research Institute, Wilhelminenhospital, Vienna, Austria. heinz.ludwig.lud@extern.wienkav.at.

Philippe Moreau (P)

University of Nantes, Nantes, France.

Meletios A Dimopoulos (MA)

National and Kapodistrian University of Athens School of Medicine, Athens, Greece.

Maria-Victoria Mateos (MV)

University Hospital Salamanca, Salamanca, Spain.

Martin Kaiser (M)

The Institute of Cancer Research, London, UK.

Roman Hajek (R)

University Hospital Ostrava and Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.

Shibao Feng (S)

Amgen Inc, Thousand Oaks, CA, USA.

Kim Cocks (K)

KCStats Consultancy, Leeds, UK.

Jaqueline Buchanan (J)

Amgen Inc, Thousand Oaks, CA, USA.

Katja Weisel (K)

Universitatsklinikum Tubingen, Tubingen, Germany.

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Classifications MeSH