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Symptomatic benefit of momelotinib in patients with myelofibrosis: Results from the SIMPLIFY phase III studies.
Mesa, Ruben A; Hudgens, Stacie; Floden, Lysbeth; Harrison, Claire N; Palmer, Jeanne; Gupta, Vikas; McLornan, Donal P; McMullin, Mary F; Kiladjian, Jean-Jaques; Foltz, Lynda; Platzbecker, Uwe; Fox, M Laura; Mead, Adam J; Ross, David M; Oh, Stephen T; Perkins, Andrew; Leahy, Michael F; Deheshi, Samineh; Donahue, Rafe; Klencke, Barbara J; Verstovsek, Srdan.
Afiliación
  • Mesa RA; Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston Salem, North Carolina, USA.
  • Hudgens S; Clinical Outcomes Solutions, Tucson, Arizona, USA.
  • Floden L; Clinical Outcomes Solutions, Tucson, Arizona, USA.
  • Harrison CN; Guy's and St. Thomas' NHS Foundation Trust, London, UK.
  • Palmer J; Mayo Clinic, Phoenix, Arizona, USA.
  • Gupta V; University Health Network, University of Toronto, Toronto, Ontario, Canada.
  • McLornan DP; Guy's and St. Thomas' NHS Foundation Trust, London, UK.
  • McMullin MF; Queens University, Belfast City Hospital Trust, Belfast, UK.
  • Kiladjian JJ; Hôpital Saint-Louis, Université de Paris, Paris, France.
  • Foltz L; St Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
  • Platzbecker U; Leipzig University Hospital, Leipzig, Germany.
  • Fox ML; Hematology Department, Hospital Universitario Vall d'Hebron, Experimental Hematology, Vall d'Hebron Institute of Oncology (VHIO), Hospital Universitario Vall d'Hebron, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
  • Mead AJ; MRC Weatherall Institute of Molecular Medicine, Oxford, UK.
  • Ross DM; Flinders Medical Centre and University, Adelaide, South Australia, Australia.
  • Oh ST; Washington University School of Medicine, St. Louis, Missouri, USA.
  • Perkins A; Alfred Hospital, Monash University, Melbourne, Victoria, Australia.
  • Leahy MF; University of Western Australia, Perth, Western Australia, Australia.
  • Deheshi S; Sierra Oncology, Plymouth, Michigan, USA.
  • Donahue R; Sierra Oncology, Plymouth, Michigan, USA.
  • Klencke BJ; Sierra Oncology, Plymouth, Michigan, USA.
  • Verstovsek S; MD Anderson Cancer Center, Houston, Texas, USA.
Cancer Med ; 12(9): 10612-10624, 2023 05.
Article en En | MEDLINE | ID: mdl-37021939
BACKGROUND: Myelofibrosis (MF)-associated constitutional symptoms can severely impact health-related quality of life. Clinical trials in MF traditionally measure symptom response to treatment as a landmark endpoint of total symptom score (TSS) reduction ≥50% from baseline. However, this dichotomous assessment provides a limited view of clinically relevant symptomatic changes. Herein we evaluated longitudinal change from baseline in TSS over the continuous 24-week period and individual symptom scores to obtain a more comprehensive understanding of symptom benefits experienced by patients with MF receiving therapy. METHODS: Longitudinal symptom change was evaluated using mixed-effect model repeated measure (MMRM) methodology with individual item-level analyses to complement the interpretation of the landmark symptom results in the completed phase III SIMPLIFY studies of momelotinib in MF. MMRM compared mean change in TSS from baseline with Week 24 using data from all patient visits. Generalized estimating equations were used to estimate item-level odds ratios using multiple predictive imputations for missing data. RESULTS: Momelotinib and ruxolitinib groups reported similar overall symptom improvements, with a TSS difference of <1.5 points between groups for each post-baseline visit in SIMPLIFY-1. In SIMPLIFY-2, the improvement in TSS observed in momelotinib-treated patients was consistent with that observed in SIMPLIFY-1, whereas progressive TSS deterioration was observed with control. Item-level scores were heterogeneous in both studies. A similar and greater proportion of momelotinib-treated patients were categorized as "improved" or "stable" compared with control in SIMPLIFY-1 and SIMPLIFY-2, respectively. Odds ratios for between-group comparison ranged from 0.75 to 1.21 in SIMPLIFY-1, demonstrating similarity in likelihood of symptom improvement. In SIMPLIFY-2, the likelihood of symptom improvement in each item was higher in the momelotinib arm. CONCLUSIONS: These findings suggest that momelotinib provides clinically relevant symptom benefits in the JAK inhibitor-naïve and JAK inhibitor-exposed settings.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Mielofibrosis Primaria / Inhibidores de las Cinasas Janus Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Med Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Mielofibrosis Primaria / Inhibidores de las Cinasas Janus Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Med Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos