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本文引用的文献

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Insights into the molecular genetics of myeloproliferative neoplasms.骨髓增殖性肿瘤的分子遗传学见解。
Am Soc Clin Oncol Educ Book. 2012:411-8. doi: 10.14694/EdBook_AM.2012.32.85.
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A double-blind, placebo-controlled trial of ruxolitinib for myelofibrosis.芦可替尼治疗骨髓纤维化的双盲、安慰剂对照试验。
N Engl J Med. 2012 Mar 1;366(9):799-807. doi: 10.1056/NEJMoa1110557.
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New mutations and pathogenesis of myeloproliferative neoplasms.骨髓增殖性肿瘤的新突变和发病机制。
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Circulating interleukin (IL)-8, IL-2R, IL-12, and IL-15 levels are independently prognostic in primary myelofibrosis: a comprehensive cytokine profiling study.循环白细胞介素 (IL)-8、IL-2R、IL-12 和 IL-15 水平在原发性骨髓纤维化中具有独立的预后价值:一项全面的细胞因子谱研究。
J Clin Oncol. 2011 Apr 1;29(10):1356-63. doi: 10.1200/JCO.2010.32.9490. Epub 2011 Feb 7.
5
Philadelphia-negative classical myeloproliferative neoplasms: critical concepts and management recommendations from European LeukemiaNet.费城阴性经典骨髓增殖性肿瘤:来自欧洲白血病网络的关键概念和管理建议。
J Clin Oncol. 2011 Feb 20;29(6):761-70. doi: 10.1200/JCO.2010.31.8436. Epub 2011 Jan 4.
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How I treat myelofibrosis.我如何治疗骨髓纤维化。
Blood. 2011 Mar 31;117(13):3494-504. doi: 10.1182/blood-2010-11-315614. Epub 2011 Jan 3.
7
DIPSS plus: a refined Dynamic International Prognostic Scoring System for primary myelofibrosis that incorporates prognostic information from karyotype, platelet count, and transfusion status.DIPSS plus:一种改良的原发性骨髓纤维化动态国际预后评分系统,纳入了核型、血小板计数和输血状态的预后信息。
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8
A dynamic prognostic model to predict survival in primary myelofibrosis: a study by the IWG-MRT (International Working Group for Myeloproliferative Neoplasms Research and Treatment).原发性骨髓纤维化患者生存的动态预后模型:国际骨髓增生性肿瘤研究和治疗工作组(IWG-MRT)的一项研究。
Blood. 2010 Mar 4;115(9):1703-8. doi: 10.1182/blood-2009-09-245837. Epub 2009 Dec 14.
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Therapeutic potential of JAK2 inhibitors.JAK2 抑制剂的治疗潜力。
Hematology Am Soc Hematol Educ Program. 2009:636-42. doi: 10.1182/asheducation-2009.1.636.
10
The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes.世界卫生组织(WHO)髓系肿瘤和急性白血病分类的2008年修订版:基本原理及重要变化
Blood. 2009 Jul 30;114(5):937-51. doi: 10.1182/blood-2009-03-209262. Epub 2009 Apr 8.

芦可替尼在各患者亚组中的临床获益:一项安慰剂对照、III 期研究中对骨髓纤维化患者的分析。

The clinical benefit of ruxolitinib across patient subgroups: analysis of a placebo-controlled, Phase III study in patients with myelofibrosis.

机构信息

The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Br J Haematol. 2013 May;161(4):508-16. doi: 10.1111/bjh.12274. Epub 2013 Mar 11.

DOI:10.1111/bjh.12274
PMID:23480528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4055021/
Abstract

Myelofibrosis (MF) patients can present with a wide spectrum of disease characteristics. We analysed the consistency of ruxolitinib efficacy across patient subgroups in the COntrolled MyeloFibrosis Study With ORal JAK Inhibitor Treatment (COMFORT-I,) a double-blind trial, where patients with intermediate-2 or high-risk MF were randomized to twice-daily oral ruxolitinib (n = 155) or placebo (n = 154). Subgroups analysed included MF subtype (primary, post-polycythaemia vera, post-essential thrombocythaemia), age (≤65, > 65 years), International Prognostic Scoring System risk group, baseline Eastern Cooperative Oncology Group performance status (0, 1, ≥2), JAK2 V617F mutation (positive, negative), baseline haemoglobin level (≥100, <100 g/l), baseline platelet count (100-200 × 10(9)/l, >200 × 10(9)/l), baseline palpable spleen size (≤10, >10 cm), and baseline quartile of spleen volume and Total Symptom Score (TSS; Q1 = lowest, Q4 = highest). Mean percentage change from baseline to week 24 in spleen volume and TSS were calculated for ruxolitinib and placebo in each subgroup. Overall survival was estimated by Kaplan-Meier method according to original randomization group. In ruxolitinib-treated patients, reductions in spleen volume and TSS and evidence of improved survival relative to placebo across subgroups were consistent with those seen in the COMFORT-I population, confirming that ruxolitinib is an effective therapy for the spectrum of MF patients studied in COMFORT-I.

摘要

骨髓纤维化 (MF) 患者可能具有广泛的疾病特征。我们分析了在对照性骨髓纤维化研究中,接受口服 JAK 抑制剂治疗的疗效一致性(COMFORT-I),这是一项双盲试验,其中中间-2 或高危 MF 患者被随机分配至每日两次口服鲁索替尼(n=155)或安慰剂(n=154)。分析的亚组包括 MF 亚型(原发性、真性红细胞增多症后、特发性血小板增多症后)、年龄(≤65 岁,>65 岁)、国际预后评分系统风险组、基线东部合作肿瘤学组表现状态(0、1、≥2)、JAK2 V617F 突变(阳性、阴性)、基线血红蛋白水平(≥100、<100 g/l)、基线血小板计数(100-200×10^9/l、>200×10^9/l)、基线可触及脾脏大小(≤10、>10 cm)以及基线脾脏体积和总症状评分(TSS)四分位数(Q1=最低,Q4=最高)。在每个亚组中,计算鲁索替尼和安慰剂从基线到第 24 周时脾脏体积和 TSS 的平均百分比变化。根据原始随机分组,采用 Kaplan-Meier 法估计总生存。在鲁索替尼治疗患者中,与安慰剂相比,在各亚组中脾脏体积和 TSS 的降低以及生存获益的证据与 COMFORT-I 人群中观察到的一致,证实鲁索替尼是 COMFORT-I 研究中所研究的 MF 患者谱的有效治疗方法。