Evidence map›Paper›PMID 37901848›Full record

ArticleHemaSphere2023

Patient-reported Outcomes and Quality of Life in Anemic and Symptomatic Patients With Myelofibrosis: Results From the MOMENTUM Study.

Ruben A Mesa, Claire Harrison, Jeanne M Palmer, Vikas Gupta, Donal P McLornan, Mary Frances McMullin, Jean-Jacques Kiladjian, Lynda Foltz, Uwe Platzbecker, Maria Laura Fox and 11 more

Open access · goldAbstract read
In one paragraph

Article in HemaSphere, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 18 institutions in 7 countries.

Ruben A MesaAtrium Health Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC, USA.
Claire HarrisonGuy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
Jeanne M PalmerMayo Clinic, Phoenix, AZ, USA.
Vikas GuptaPrincess Margaret Cancer Centre, University of Toronto, ON, Canada.
Donal P McLornanGuy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
Mary Frances McMullinQueen's University, Belfast, United Kingdom.
Jean-Jacques KiladjianUniversité de Paris, AP-HP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, Paris, France.
Lynda FoltzUniversity of British Columbia, Vancouver, BC, Canada.
Uwe PlatzbeckerUniversity Hospital Leipzig, Germany.
Maria Laura FoxServei d'Hematologia, Vall d'Hebron Hospital Universitari, Experimental Hematology, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
Adam J MeadOxford University Hospitals NHS Foundation Trust, United Kingdom.
David M RossFlinders Medical Centre and SA Pathology, Adelaide, SA, Australia.
Stephen T OhWashington University School of Medicine, St Louis, MO, USA.
Andrew Charles PerkinsThe Alfred Hospital and Australian Centre for Blood Diseases, Monash University, Melbourne, VIC, Australia.
Michael F LeahyRoyal Perth Hospital, PathWest Laboratory Medicine; University of Western Australia, Perth, WA, Australia.
Jun KawashimaSierra Oncology, Inc., a GSK company, San Mateo, CA, USA.
Sunhee RoSierra Oncology, Inc., a GSK company, San Mateo, CA, USA.
Rafe DonahueSierra Oncology, Inc., a GSK company, San Mateo, CA, USA.
Boris GorshGSK, Philadelphia, PA, USA.
Samineh DeheshiSierra Oncology, Inc., a GSK company, San Mateo, CA, USA.
Srdan VerstovsekThe University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Sierra Engineering (United States) · USAtrium Medical Cente · USFlinders Medical Centre · AUGlaxoSmithKline (United States) · USGuy's and St Thomas' NHS Foundation Trust · GBMayo Clinic Hospital · USMonash University · AUOxford University Hospitals NHS Trust · GBPrincess Margaret Cancer Centre · CAQueen's University Belfast · GBThe University of Texas MD Anderson Cancer Center · USThe University of Western Australia · AUUniversité Paris Cité · FRUniversity College Hospital · GBUniversity Hospital Leipzig · DEUniversity of British Columbia · CAVall d'Hebron Hospital Universitari · ESWashington University in St. Louis · US

Funding

Cancer Research UK 26988Cancer Research UK 27125Cancer Research UK 27723
6 · The paper itself

Abstract

Myelofibrosis (MF) is a chronic myeloproliferative neoplasm that typically manifests with debilitating symptoms that progressively worsen, negatively impacting patients' quality of life. Fatigue is a multifactorial and burdensome MF-related symptom due to its severity, persistence, and prevalence, with anemia a contributing factor and major unmet need. Clinical trials of the Janus kinase (JAK)1/JAK2/activin A receptor type 1 inhibitor momelotinib have shown consistent anemia benefits, in addition to improvements in MF-related symptoms. The phase 3 MOMENTUM trial in symptomatic and anemic patients met its primary end point, with a greater proportion having a Myelofibrosis Symptom Assessment Form (MFSAF) Total Symptom Score (TSS) reduction ≥50% at week 24 with momelotinib versus danazol. To support the positive primary end point result, we conducted longitudinal, responder, and time-to-event analyses of patient-reported outcomes from MOMENTUM, as measured by the MFSAF, European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30), and Patient-Reported Outcomes Measurement Information System (PROMIS) assessments. These analyses demonstrated rapid and durable response benefits with momelotinib, with achievement of first TSS response by day 29 and continued improvement over time. Improvements favored momelotinib versus danazol for each MFSAF individual item, and greater improvements were observed for disease- and cancer-related fatigue and physical functioning at week 24, with significant results for multiple items/domains across the 3 assessments. These findings are consistent in demonstrating that momelotinib provides substantial symptom benefit.

Identifiers

PMID37901848
PMCPMC10599984
OpenAlexW4387899802

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.