Momelotinib versus danazol in symptomatic patients with anaemia and myelofibrosis (MOMENTUM): results from an international, double-blind, randomised, controlled, phase 3 study.

BACKGROUND

Janus kinase (JAK) inhibitors approved for myelofibrosis provide spleen and symptom improvements but do not meaningfully improve anaemia. Momelotinib, a first-in-class inhibitor of activin A receptor type 1 as well as JAK1 and JAK2, has shown symptom, spleen, and anaemia benefits in myelofibrosis. We aimed to confirm the differentiated clinical benefits of momelotinib versus the active comparator danazol in JAK-inhibitor-exposed, symptomatic patients with anaemia and intermediate-risk or high-risk myelofibrosis.

METHODS

MOMENTUM is an international, double-blind, randomised, controlled, phase 3 study that enrolled patients at 107 sites across 21 countries worldwide. Eligible patients were 18 years or older with a confirmed diagnosis of primary myelofibrosis or post-polycythaemia vera or post-essential thrombocythaemia myelofibrosis. Patients were randomly assigned (2:1) to receive momelotinib (200 mg orally once per day) plus danazol placebo (ie, the momelotinib group) or danazol (300 mg orally twice per day) plus momelotinib placebo (ie, the danazol group), stratified by total symptom score (TSS; <22 vs ≥22), spleen size (<12 cm vs ≥12 cm), red blood cell or whole blood units transfused in the 8 weeks before randomisation (0 units vs 1-4 units vs ≥5 units), and study site. The primary endpoint was the Myelofibrosis Symptom Assessment Form (MFSAF) TSS response rate at week 24 (defined as ≥50% reduction in mean MFSAF TSS over the 28 days immediately before the end of week 24 compared with baseline). MOMENTUM is registered with ClinicalTrials.gov, number NCT04173494, and is active but not recruiting.

FINDINGS

195 patients were randomly assigned to either the momelotinib group (130 [67%]) or danazol group (65 [33%]) and received study treatment in the 24-week randomised treatment period between April 24, 2020, and Dec 3, 2021. A significantly greater proportion of patients in the momelotinib group reported a 50% or more reduction in TSS than in the danazol group (32 [25%] of 130 vs six [9%] of 65; proportion difference 16% [95% CI 6-26], p=0·0095). The most frequent grade 3 or higher treatment-emergent adverse events with momelotinib and danazol were haematological abnormalities by laboratory values: anaemia (79 [61%] of 130 vs 49 [75%] of 65) and thrombocytopenia (36 [28%] vs 17 [26%]). The most frequent non-haematological grade 3 or higher treatment-emergent adverse events with momelotinib and danazol were acute kidney injury (four [3%] of 130 vs six [9%] of 65) and pneumonia (three [2%] vs six [9%]).

INTERPRETATION

Treatment with momelotinib, compared with danazol, resulted in clinically significant improvements in myelofibrosis-associated symptoms, anaemia measures, and spleen response, with favourable safety. These findings support the future use of momelotinib as an effective treatment in patients with myelofibrosis, especially in those with anaemia.

FUNDING

Sierra Oncology.

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests SV reports consulting fees from Bristol Myers Squibb/Celgene, Incyte, Novartis, and Sierra Oncology. ATG reports consulting fees from AbbVie, Bristol Myers Squibb, Constellation/MorphoSys, CTI Biopharma, Novartis, Pharma Essentia, and Sierra Oncology. ATK reports grants from AbbVie, Bristol Myers Squibb, Prelude, and Sierra; consulting fees from AbbVie and Prelude; honoraria from Bristol Myers Squibb, Incyte, and Novartis; and participation on a data safety monitoring board or advisory board for AbbVie, Bristol Myers Squibb, CTI Biopharma, Geron, Imago, and Incyte. MLF reports payment for expert testimony from OncLive; meeting attendance or travel support from Novartis; and participation on a data safety monitoring board or advisory board for Bristol Myers Squibb, Novartis, and Sierra Oncology. DM reports research grants from Bristol Myers Squibb/Celgene, and Constellation Biopharma; honoraria from AbbVie, Celgene, Jazz, and Novartis; meeting attendance or travel support from Jazz; participation on a data safety monitoring board or advisory board for the ALL-RIC study; and leadership role with the European Society of Hematology and the EBMT Chronic Malignancies Working Party. AP reports honoraria, meeting attendance and travel support, and participation on an advisory board from Novartis Oncology. S-SY reports research grants from Kyowa Kirin and Roche/Genentech; consulting fees from Astellas, Amgen, Antengene, and Celgene; and honoraria from Novartis. VG reports consulting fees from AbbVie, Bristol Myers Squibb/Celgene, Constellation Biopharma, Novartis, Pfizer, and Sierra Oncology; honoraria from Bristol Myers Squibb, Constellation Biopharma, and Novartis; and participation on data safety monitoring board or advisory board for AbbVie, Bristol Myers Squibb/Celgene, Pfizer, and Roche. J-JK reports honoraria from Novartis; participation on a data safety monitoring board or advisory board for AbbVie, Bristol Myers Squibb, Incyte, and Novartis. NG reports consulting fees from Alexion, Bristol Myers Squibb/Celgene, Incyte, and Novartis; honoraria from Bristol Myers Squibb/Celgene, Janssen, and Novartis; leadership or fiduciary role for Alexion, Incyte, and Novartis; and meeting attendance or travel support from AbbVie, Genzyme, and Sanofi. FP reports research grant from Bristol Myers Squibb/Celgene; consulting fees from AbbVie, APO, Bristol Myers Squibb/Celgene, Karyopharm, Kyowa Kirin, MEI, Novartis, and Roche; and honoraria from Bristol Myers Squibb/Celgene, Janssen, and Novartis. CNH reports grant support from Bristol Myers Squibb/Celgene, Constellation Biopharma, and Novartis; consulting fees from AOP, Galecto, Keros, and Roche; honoraria from AbbVie, Celgene, Constellation Biopharma, CTI Biopharma, Janssen, and Novartis; participation in data safety monitoring board or advisory board for AbbVie, AOP, CTI Biopharma, Geron, Promedior, Roche, and Sierra Oncology; and leadership or fiduciary role in the European Hematology Association and MPN Voice. BJK, SR, and RD report employment and stock or stock options at Sierra Oncology. JK reports employment and stock or stock options at Sierra Oncology and former employment and stock and stock options from Gilead. RM reports research grants from AbbVie, Celgene, CTI Biopharma, Constellation Biopharma, Genotech, Incyte, Promedior, Samus, and the Mays Cancer Center P30 Cancer Center Support Grant from the National Cancer Institute (CA054174); and consulting fees from Constellation Biopharma, LaJolla, Novartis, and Sierra Oncology. All other authors declare no competing interests.