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Efficacy of Momelotinib in Myelofibrosis Patients: Results From a Multicenter Study.

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European journal of haematology 📖 저널 OA 58.9% 2025: 2/10 OA 2026: 41/63 OA 2025~2026 2026 Vol.116(1) p. 23-30 OA
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PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
환자: myelofibrosis (MF) and anemia, a disease-related manifestation of challenging management
I · Intervention 중재 / 시술
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C · Comparison 대조 / 비교
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O · Outcome 결과 / 결론
In conclusion, our real-life results support the use of momelotinib as an effective and safe therapeutic option for heavily pre-treated, cytopenic MF patients in real-world clinical practice.

Martorelli MC, Pugliese N, Di Perna M, De Novellis D, Lombardi A, De Fazio L

📝 환자 설명용 한 줄

Momelotinib, a novel JAK1/2 inhibitor with inhibitory activities on activin A receptor type I, has shown breakthrough clinical efficacy in patients with myelofibrosis (MF) and anemia, a disease-relate

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APA Martorelli MC, Pugliese N, et al. (2026). Efficacy of Momelotinib in Myelofibrosis Patients: Results From a Multicenter Study.. European journal of haematology, 116(1), 23-30. https://doi.org/10.1111/ejh.70034
MLA Martorelli MC, et al.. "Efficacy of Momelotinib in Myelofibrosis Patients: Results From a Multicenter Study.." European journal of haematology, vol. 116, no. 1, 2026, pp. 23-30.
PMID 40955124 ↗
DOI 10.1111/ejh.70034

Abstract

Momelotinib, a novel JAK1/2 inhibitor with inhibitory activities on activin A receptor type I, has shown breakthrough clinical efficacy in patients with myelofibrosis (MF) and anemia, a disease-related manifestation of challenging management. In this retrospective real-life multicenter Italian study, we investigated the safety and efficacy of momelotinib in a cohort of 39 consecutive MF patients, regardless of prior therapy. The median duration of treatment was 7 months, and the overall response rate was 56% in transfusion-dependent patients and 46% in the transfusion-independent group. At 24 weeks of treatment, a hemoglobin increase > 1.5 g/dL was observed in 26% of patients, and constitutional symptom improvement was reported in 51% of cases, with a spleen volume reduction > 35% in 28%. Therapy discontinuation occurred in 18% of patients, with only one leukemia progression and three deaths during follow-up. The safety profile was similar to that reported in clinical trials, with most toxicities of grade I-II. In conclusion, our real-life results support the use of momelotinib as an effective and safe therapeutic option for heavily pre-treated, cytopenic MF patients in real-world clinical practice.

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