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Meaningful Symptomatic Change in Patients With Myelofibrosis From the SIMPLIFY Studies.
Hudgens, Stacie; Verstovsek, Srdan; Floden, Lysbeth; Harrison, Claire N; Palmer, Jeanne; Gupta, Vikas; McLornan, Donal; McMullin, Mary Frances; Kiladjian, Jean-Jacques; Foltz, Lynda; Platzbecker, Uwe; Fox, Maria Laura; Mead, Adam J; Ross, David M; Oh, Stephen T; Perkins, Andrew A; Leahy, Michael F; Deheshi, Samineh; Donahue, Rafe; Klencke, Barbara J; Mesa, Ruben A.
Afiliação
  • Hudgens S; Clinical Outcomes Solutions, Tucson, AZ, USA. Electronic address: stacie.hudgens@clinoutsolutions.com.
  • Verstovsek S; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Floden L; Clinical Outcomes Solutions, Tucson, AZ, USA.
  • Harrison CN; Department of Haematology, Guy's and St. Thomas' National Health Service Foundation Trust, London, England, UK.
  • Palmer J; Department of Hematology, Mayo Clinic, Phoenix, AZ, USA.
  • Gupta V; Princess Margaret Cancer Center, University Health Network, University of Toronto, Toronto, ON, Canada.
  • McLornan D; Department of Haematology, Guy's and St. Thomas' National Health Service Foundation Trust, London, England, UK.
  • McMullin MF; School of Medicine, Dentistry and Biomedical Sciences, Queens University, Belfast City Hospital Trust, Belfast, Northern Ireland, UK.
  • Kiladjian JJ; Université de Paris, AP-HP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM, Paris, France.
  • Foltz L; Department of Medicine, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
  • Platzbecker U; Department of Hematology, Hemostaseology, Cellular Therapy and Infectiology, Leipzig University Hospital, Leipzig, Germany.
  • Fox ML; Department of Haematology, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron University Hospital, Barcelona, Spain.
  • Mead AJ; MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, Oxford, England, UK.
  • Ross DM; College of Medicine and Public Health, Flinders Medical Centre and University, Adelaide, SA, Australia.
  • Oh ST; Division of Hematology, Washington University School of Medicine, St. Louis, MO, USA.
  • Perkins AA; Department of Haematology, Alfred Hospital and Monash University, Melbourne, VIC, Australia.
  • Leahy MF; Department of Haematology, University of Western Australia, Perth, WA, Australia.
  • Deheshi S; Sierra Oncology, a GSK company, San Mateo, CA, USA.
  • Donahue R; Sierra Oncology, a GSK company, San Mateo, CA, USA.
  • Klencke BJ; Sierra Oncology, a GSK company, San Mateo, CA, USA.
  • Mesa RA; Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Value Health ; 27(5): 607-613, 2024 May.
Article em En | MEDLINE | ID: mdl-38311180
ABSTRACT

OBJECTIVES:

Patients with myelofibrosis develop symptoms due to bone marrow fibrosis, systemic inflammation, and/or organomegaly. Alleviating symptoms improves overall quality of life. Clinical trials have historically defined symptom response as a reduction of at least 50% in Total Symptom Score at week 24 compared with baseline. Whether 50% constitutes a meaningful benefit has not been established. This study determined the meaningful change threshold (MCT) for 2 momelotinib phase III trials, SIMPLIFY-1 and SIMPLIFY-2.

METHODS:

The absolute and percentage MCT was determined using anchor-based methods applied to the modified Myeloproliferative Neoplasm Symptom Assessment Form v2.0 and Patient Global Impression of Change. MCTs were applied retrospectively to determine responder rates. Generalized estimating equations estimated the treatment-related difference in likelihood of improvement.

RESULTS:

In SIMPLIFY-1, a Janus kinase inhibitor-naive population, the MCT was 8 points. In SIMPLIFY-2, a previously Janus kinase inhibitor-treated population, the MCT was 6 points. A 32% MCT was determined in both studies, showing that the historic 50% reduction threshold may be a conservative choice. In SIMPLIFY-1, a similar proportion of patients achieved responder status with 24 weeks of momelotinib or ruxolitinib therapy based on the absolute MCT (39% vs 41%, respectively). In SIMPLIFY-2, a significantly greater proportion of patients treated with momelotinib achieved responder states compared with best available therapy based on absolute and percent change MCTs.

CONCLUSIONS:

This study demonstrates that momelotinib provided clinically meaningful symptom benefit for patients with myelofibrosis and provides insight into the appropriateness of the symptom change threshold used in historical studies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirimidinas / Qualidade de Vida / Mielofibrose Primária Tipo de estudo: Diagnostic_studies Aspecto: Patient_preference Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Value Health Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirimidinas / Qualidade de Vida / Mielofibrose Primária Tipo de estudo: Diagnostic_studies Aspecto: Patient_preference Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Value Health Ano de publicação: 2024 Tipo de documento: Article