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Health-Related Quality of Life in Transplant-Ineligible Patients With Newly Diagnosed Multiple Myeloma: Findings From the Phase III MAIA Trial.
Perrot, Aurore; Facon, Thierry; Plesner, Torben; Usmani, Saad Z; Kumar, Shaji; Bahlis, Nizar J; Hulin, Cyrille; Orlowski, Robert Z; Nahi, Hareth; Mollee, Peter; Ramasamy, Karthik; Roussel, Murielle; Jaccard, Arnaud; Delforge, Michel; Karlin, Lionel; Arnulf, Bertrand; Chari, Ajai; He, Jianming; Ho, Kai Fai; Van Rampelbergh, Rian; Uhlar, Clarissa M; Wang, Jianping; Kobos, Rachel; Gries, Katharine S; Fastenau, John; Weisel, Katja.
Afiliação
  • Perrot A; Hematology Department, Cancer University Institute Oncopole, Toulouse, France.
  • Facon T; Service des Maladies du Sang, Hôpital Claude Huriez, Lille, France.
  • Plesner T; Vejle Hospital and University of Southern Denmark, Vejle, Denmark.
  • Usmani SZ; Levine Cancer Institute/Atrium Health, Charlotte, NC.
  • Kumar S; Department of Hematology, Mayo Clinic Rochester, Rochester, MN.
  • Bahlis NJ; University of Calgary, Arnie Charbonneau Cancer Research Institute, Calgary, AB, Canada.
  • Hulin C; Department of Hematology, Hospital Haut Leveque, University Hospital, Pessac, France.
  • Orlowski RZ; Department of Lymphoma-Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Nahi H; Division of Hematology, Department of Medicine, Karolinska Institute, Karolinska University Hospital at Huddinge, Stockholm, Sweden.
  • Mollee P; Princess Alexandra Hospital and University of Queensland, Brisbane, Australia.
  • Ramasamy K; Oxford University Hospital and NIHR BRC Blood Theme, Oxford, United Kingdom.
  • Roussel M; Hematology Department, Cancer University Institute Oncopole, Toulouse, France.
  • Jaccard A; Centre Hospitalier Universitaire, Limoges, France.
  • Delforge M; Department of Hematology, University Hospital Leuven, Belgium.
  • Karlin L; Centre Hospitalier Lyon-Sud Hematologie (HCL), Pierre-Benite Cedex, France.
  • Arnulf B; Hematology/Oncology, Hopital Saint Louis, Paris, France.
  • Chari A; Tisch Cancer Institute, Mount Sinai School of Medicine, New York, NY.
  • He J; Janssen Global Services, Raritan, NJ.
  • Ho KF; STAT-TU Inc, Toronto, ON, Canada.
  • Van Rampelbergh R; Janssen Research & Development, Beerse, Belgium.
  • Uhlar CM; Janssen Research & Development, Raritan, NJ.
  • Wang J; Janssen Research & Development, Raritan, NJ.
  • Kobos R; Janssen Research & Development, Raritan, NJ.
  • Gries KS; Janssen Global Services, Raritan, NJ.
  • Fastenau J; Janssen Global Services, Raritan, NJ.
  • Weisel K; Department of Oncology, Hematology, BMT with Department of Pneumology, University Medical Center Hamburg, Hamburg, Germany.
J Clin Oncol ; 39(3): 227-237, 2021 01 20.
Article em En | MEDLINE | ID: mdl-33326255
ABSTRACT

PURPOSE:

To evaluate the effects of daratumumab, lenalidomide, and dexamethasone (D-Rd) versus lenalidomide and dexamethasone (Rd) on patient-reported outcomes (PROs) in the phase III MAIA study. PATIENTS AND

METHODS:

PROs were assessed on the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30-item and the EuroQol 5-dimensional descriptive system at baseline and every 3 months during treatment. By mixed-effects model, changes from baseline are presented as least squares means with 95% CIs.

RESULTS:

A total of 737 transplant-ineligible (TIE) patients with newly diagnosed multiple myeloma were randomly assigned to D-Rd (n = 368) or Rd (n = 369). Compliance with PRO assessments was high at baseline (> 90%) through month 12 (> 78%) for both groups. European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30-item global health status scores improved from baseline in both groups and were consistently greater with D-Rd at all time points. A global health status benefit was achieved with D-Rd, regardless of age (< 75 and ≥ 75 years), baseline Eastern Cooperative Oncology Group (ECOG) performance status score, or depth of response. D-Rd treatment resulted in significantly greater reduction in pain scores as early as cycle 3 (P = .0007 v Rd); the magnitude of change was sustained through cycle 12. Reductions in pain with D-Rd were clinically meaningful in patients regardless of age, ECOG status, or depth of response. Similarly, PRO improvements were observed with D-Rd and Rd on the EuroQol 5-dimensional descriptive system visual analog scale score.

CONCLUSION:

D-Rd compared with Rd was associated with faster and sustained clinically meaningful improvements in PROs, including pain, in transplant-ineligible patients with newly diagnosed multiple myeloma regardless of age, baseline ECOG status, or depth of treatment response.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Dexametasona / Protocolos de Quimioterapia Combinada Antineoplásica / Medidas de Resultados Relatados pelo Paciente / Lenalidomida / Anticorpos Monoclonais / Mieloma Múltiplo Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Aspecto: Patient_preference Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Oncol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Dexametasona / Protocolos de Quimioterapia Combinada Antineoplásica / Medidas de Resultados Relatados pelo Paciente / Lenalidomida / Anticorpos Monoclonais / Mieloma Múltiplo Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Aspecto: Patient_preference Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Oncol Ano de publicação: 2021 Tipo de documento: Article