Overall survival with momelotinib vs. best available therapy in patients with ruxolitinib-experienced myelofibrosis: a matching-adjusted indirect comparison

The Janus kinase (JAK) inhibitor ruxolitinib is a standard first-line therapy for patients with symptomatic and/or intermediate- to high-risk myelofibrosis (MF). However, the majority of patients discontinue ruxolitinib within 5 years of initiation, mainly due to lack or loss of response and/or therapy-related cytopenias. Additional treatments are needed to improve long-term outcomes, including overall survival (OS). Momelotinib, a JAK1/JAK2/activin A receptor type 1 inhibitor, has demonstrated benefits in reducing anemia and improving symptoms and spleen size in 3 phase 3 trials of patients with intermediate- to high-risk MF (SIMPLIFY-1, SIMPLIFY-2, and MOMENTUM). These studies also provide data on patients who received momelotinib after discontinuing ruxolitinib. In the absence of long-term head-to-head comparisons of momelotinib and other treatments after discontinuation of ruxolitinib, the present study compared OS in patients with ruxolitinib-experienced MF from the momelotinib phase 3 trials vs. those treated with best available therapy (BAT) after ruxolitinib from the RUX-MF retrospective real-world study. The comparison was performed using an unanchored matching-adjusted indirect comparison (MAIC). Additionally, an MAIC of OS was conducted in an anemic subgroup (hemoglobin < 10 g/dL). After adjustment for cross-trial differences, the MAIC results showed a favorable trend for momelotinib vs. BAT, both in the overall population and in the anemic subgroup, with hazard ratios < 1 across all analytical scenarios and all population-matching models with an effective sample size of ≥ 20. This study is a key addition to current evidence surrounding OS post ruxolitinib and highlights the benefit of momelotinib in this setting.

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Publication Details

Journal
Annals of Hematology
Published
2026-02-21
DOI
https://doi.org/10.1007/s00277-026-06873-w
Primary Topic
Myeloproliferative Neoplasms: Diagnosis and Treatment
Type
article
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article

Overall survival with momelotinib vs. best available therapy in patients with ruxolitinib-experienced myelofibrosis: a matching-adjusted indirect comparison

Nick Ballew, E. Abruzzese, Kelesitse Phiri, Fulya Sen Nikitas et al.
Annals of Hematology
Myeloproliferative Neoplasms: Diagnosis and Treatment
article

Overall survival with momelotinib vs. best available therapy in patients with ruxolitinib-experienced myelofibrosis: a matching-adjusted indirect comparison

Nick Ballew, E. Abruzzese, Kelesitse Phiri, Fulya Sen Nikitas, Balázs Dobi, Tom Liu, Shiyuan Zhang, Erika Morsia, Dwaipayan Patnaik, Filippo Branzanti, Elena Maria Elli, Catherine E. Ellis, Massimiliano Bonifacio, Francesca Palandri, Venediktos Kapetanakis, Massimo Breccia, Mario Tiribelli, Giuseppe A. Palumbo
article en

Abstract

The Janus kinase (JAK) inhibitor ruxolitinib is a standard first-line therapy for patients with symptomatic and/or intermediate- to high-risk myelofibrosis (MF). However, the majority of patients discontinue ruxolitinib within 5 years of initiation, mainly due to lack or loss of response and/or therapy-related cytopenias. Additional treatments are needed to improve long-term outcomes, including overall survival (OS). Momelotinib, a JAK1/JAK2/activin A receptor type 1 inhibitor, has demonstrated benefits in reducing anemia and improving symptoms and spleen size in 3 phase 3 trials of patients with intermediate- to high-risk MF (SIMPLIFY-1, SIMPLIFY-2, and MOMENTUM). These studies also provide data on patients who received momelotinib after discontinuing ruxolitinib. In the absence of long-term head-to-head comparisons of momelotinib and other treatments after discontinuation of ruxolitinib, the present study compared OS in patients with ruxolitinib-experienced MF from the momelotinib phase 3 trials vs. those treated with best available therapy (BAT) after ruxolitinib from the RUX-MF retrospective real-world study. The comparison was performed using an unanchored matching-adjusted indirect comparison (MAIC). Additionally, an MAIC of OS was conducted in an anemic subgroup (hemoglobin < 10 g/dL). After adjustment for cross-trial differences, the MAIC results showed a favorable trend for momelotinib vs. BAT, both in the overall population and in the anemic subgroup, with hazard ratios < 1 across all analytical scenarios and all population-matching models with an effective sample size of ≥ 20. This study is a key addition to current evidence surrounding OS post ruxolitinib and highlights the benefit of momelotinib in this setting.

Annals of HematologyVol. 105(4)
University of Verona (IT), Marche Polytechnic University (IT), University of Udine (IT), Policlinico Umberto I (IT), University of Catania (IT), Azienda Ospedaliera San Gerardo (IT), GlaxoSmithKline (United States) (US), Istituto di Ematologia di Bologna (IT), Azienda USL di Bologna (IT), EVRAZ (United Kingdom) (GB), Tecnologie Avanzate (Italy) (IT), Geotechnical Consulting Group (United Kingdom) (GB), St. Eugenio Hospital (IT), Amt für Gemeinden und Raumordnung (CH), University of Bologna (IT)
Openalex Percentile: Top 48%
Myeloproliferative Neoplasms: Diagnosis and Treatment
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