Longitudinal Assessment of Transfusion Intensity in Patients With JAK Inhibitor-Naive or -Experienced Myelofibrosis Treated With Momelotinib.

IF 2.7 4区 医学 Q2 HEMATOLOGY Clinical Lymphoma, Myeloma & Leukemia Pub Date : 2024-10-16 DOI:10.1016/j.clml.2024.10.001
Claire N Harrison, Ruben Mesa, Moshe Talpaz, Vikas Gupta, Aaron T Gerds, Andrew Perkins, Yeow Tee Goh, Maria Laura Fox, Donal McLornan, Jeanne Palmer, Lynda Foltz, Alessandro Vannucchi, Steffen Koschmieder, Francesco Passamonti, Sung-Eun Lee, Catherine Ellis, Bryan Strouse, Francisco J Gonzalez Carreras, Stephen T Oh
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Abstract

Purpose: Anemia is a cardinal feature of myelofibrosis often managed with red blood cell (RBC) transfusions, which may contribute to negative prognostic, quality-of-life, and healthcare-related economic impacts. The Janus kinase (JAK) 1/JAK2/activin A receptor type 1 inhibitor momelotinib was approved for the treatment of patients with myelofibrosis and anemia based on clinical trial evidence of anemia, spleen, and symptom benefits illustrated using binomial response/nonresponse endpoints. In the present post hoc, descriptive analyses, the impact of momelotinib on RBC transfusion burden over time was further characterized across JAK inhibitor-naive and -experienced patients.

Methods: All RBC units transfused were collected during the baseline and 24-week treatment periods, initially in a single-arm phase 2 study as proof-of-concept analysis, and then versus comparators (ruxolitinib, best available therapy [BAT], and danazol) in the phase 3 SIMPLIFY-1, SIMPLIFY-2, and MOMENTUM studies, respectively.

Results: In the phase 2 study, mean transfusion requirement changed by -1.5 units/28 days, with 85% of patients (35/41) achieving numeric transfusion reduction. Across SIMPLIFY-1, SIMPLIFY-2, and MOMENTUM, mean transfusion requirements decreased with momelotinib (-0.1, -0.36, and -0.86 units/28 days), while mean requirements with ruxolitinib, BAT, and danazol changed by +0.39, 0, and ‒0.28 units/28 days, respectively. Overall, 87% (185/213), 77% (79/103), and 85% (110/130) of patients had improved or stable transfusion intensities with momelotinib versus 54% (117/216), 62% (32/52), and 63% (41/65) with ruxolitinib, BAT, and danazol.

Conclusion: These novel time-dependent transfusion burden analyses demonstrate that momelotinib is associated with anemia-related benefits in most patients and greater transfusion burden reduction versus comparators.

Trial registration: ClinicalTrials.gov identifiers: NCT02515630, NCT01969838, NCT02101268, NCT04173494.

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对接受莫美洛替尼治疗的 JAK 抑制剂无效或有经验骨髓纤维化患者输血强度的纵向评估
目的:贫血是骨髓纤维化的一个主要特征,通常需要输注红细胞(RBC),这可能会对预后、生活质量和医疗相关经济产生负面影响。Janus激酶(JAK)1/JAK2/活性蛋白A受体1型抑制剂莫美洛替尼被批准用于骨髓纤维化贫血患者的治疗,其依据是临床试验的证据,即使用二项式反应/无反应终点说明贫血、脾脏和症状的益处。在本研究的事后描述性分析中,进一步分析了莫美洛替尼对JAK抑制剂无效和有经验患者的RBC输血负担的影响:在基线和24周治疗期间收集所有输注的红细胞单位,最初在单臂2期研究中进行概念验证分析,然后在3期SIMPLIFY-1、SIMPLIFY-2和MOMENTUM研究中分别与比较者(鲁索利替尼、最佳可用疗法[BAT]和达那唑)进行比较:结果:在第二阶段研究中,平均输血量减少了-1.5个单位/28天,85%的患者(35/41)输血量减少。在SIMPLIFY-1、SIMPLIFY-2和MOMENTUM中,莫美洛替尼的平均输血量减少了(-0.1、-0.36和-0.86单位/28天),而鲁索利替、BAT和达那唑的平均输血量分别减少了+0.39、0和-0.28单位/28天。总体而言,87%(185/213)、77%(79/103)和85%(110/130)的患者使用莫美洛替尼后输血强度有所改善或保持稳定,而使用鲁索利替尼、BAT和达那唑时则分别为54%(117/216)、62%(32/52)和63%(41/65):这些新的时间依赖性输血负担分析表明,莫迈罗替尼对大多数患者都有贫血相关的益处,与比较药相比,莫迈罗替尼可更大程度地减轻输血负担:试验注册:ClinicalTrials.gov identifiers:NCT02515630、NCT01969838、NCT02101268、NCT04173494。
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来源期刊
CiteScore
2.70
自引率
3.70%
发文量
1606
审稿时长
26 days
期刊介绍: Clinical Lymphoma, Myeloma & Leukemia is a peer-reviewed monthly journal that publishes original articles describing various aspects of clinical and translational research of lymphoma, myeloma and leukemia. Clinical Lymphoma, Myeloma & Leukemia is devoted to articles on detection, diagnosis, prevention, and treatment of lymphoma, myeloma, leukemia and related disorders including macroglobulinemia, amyloidosis, and plasma-cell dyscrasias. The main emphasis is on recent scientific developments in all areas related to lymphoma, myeloma and leukemia. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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