• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Highlights from MPN Asia 2025: Advances in Molecular Pathogenesis and Therapeutic Strategies in Myeloproliferative Neoplasms.2025年亚洲骨髓增殖性肿瘤大会亮点:骨髓增殖性肿瘤分子发病机制与治疗策略的进展
Curr Hematol Malig Rep. 2025 Jul 12;20(1):9. doi: 10.1007/s11899-025-00752-3.
2
Prescription of Controlled Substances: Benefits and Risks管制药品的处方:益处与风险
3
Management of urinary stones by experts in stone disease (ESD 2025).结石病专家对尿路结石的管理(2025年结石病专家共识)
Arch Ital Urol Androl. 2025 Jun 30;97(2):14085. doi: 10.4081/aiua.2025.14085.
4
[A new era in the treatment of myeloproliferative neoplasms].[骨髓增殖性肿瘤治疗的新时代]
Rinsho Ketsueki. 2025;66(7):597-610. doi: 10.11406/rinketsu.66.597.
5
Diagnosis and treatment of MPN in real life: exploratory and retrospective chart review including 960 MPN patients diagnosed with ET or MF in Germany.真实世界中骨髓增殖性肿瘤的诊断和治疗:探索性和回顾性图表审查,包括在德国诊断为 ET 或 MF 的 960 例 MPN 患者。
J Cancer Res Clin Oncol. 2023 Aug;149(10):7197-7206. doi: 10.1007/s00432-023-04669-3. Epub 2023 Mar 8.
6
Exposure-efficacy and exposure-safety analyses of ropeginterferon alfa-2b treatment in patients with polycythaemia vera.聚乙二醇干扰素α-2b治疗真性红细胞增多症患者的暴露-疗效和暴露-安全性分析。
Br J Clin Pharmacol. 2024 Jun;90(6):1493-1502. doi: 10.1111/bcp.16043. Epub 2024 Mar 19.
7
Systemic treatments for metastatic cutaneous melanoma.转移性皮肤黑色素瘤的全身治疗
Cochrane Database Syst Rev. 2018 Feb 6;2(2):CD011123. doi: 10.1002/14651858.CD011123.pub2.
8
Real-World Evidence on Outcomes and Safety of Ropeginterferon Alfa-2b in Patients With Myeloproliferative Neoplasms: A Retrospective Cohort Study.真性红细胞增多症患者使用聚乙二醇干扰素α-2b的疗效和安全性的真实世界证据:一项回顾性队列研究
Clin Lymphoma Myeloma Leuk. 2025 Jun 25. doi: 10.1016/j.clml.2025.06.011.
9
Adefovir dipivoxil and pegylated interferon alfa-2a for the treatment of chronic hepatitis B: a systematic review and economic evaluation.阿德福韦酯与聚乙二醇化干扰素α-2a治疗慢性乙型肝炎:系统评价与经济学评估
Health Technol Assess. 2006 Aug;10(28):iii-iv, xi-xiv, 1-183. doi: 10.3310/hta10280.
10
Interventions to improve safe and effective medicines use by consumers: an overview of systematic reviews.改善消费者安全有效用药的干预措施:系统评价概述
Cochrane Database Syst Rev. 2014 Apr 29;2014(4):CD007768. doi: 10.1002/14651858.CD007768.pub3.

本文引用的文献

1
Hematologic and molecular responses to ropeginterferon alfa-2b therapy of polycythemia vera: 48-week results from a prospective study.真性红细胞增多症患者接受聚乙二醇干扰素α-2b治疗的血液学和分子学反应:一项前瞻性研究的48周结果
Int J Cancer. 2025 Aug 1;157(3):526-533. doi: 10.1002/ijc.35411. Epub 2025 Mar 15.
2
Impact of treatment for adolescent and young adults with essential thrombocythemia and polycythemia vera.治疗对青少年及年轻成人原发性血小板增多症和真性红细胞增多症的影响。
Leukemia. 2025 May;39(5):1135-1145. doi: 10.1038/s41375-025-02545-2. Epub 2025 Mar 12.
3
Pelabresib plus ruxolitinib for JAK inhibitor-naive myelofibrosis: a randomized phase 3 trial.培拉布瑞西布联合鲁索替尼用于初治的骨髓纤维化:一项随机3期试验。
Nat Med. 2025 May;31(5):1531-1538. doi: 10.1038/s41591-025-03572-3. Epub 2025 Mar 10.
4
Selinexor plus ruxolitinib in JAK inhibitor treatment-naïve myelofibrosis: SENTRY Phase 3 study design.塞利尼索联合鲁索替尼用于初治骨髓纤维化的JAK抑制剂治疗:哨兵3期研究设计。
Future Oncol. 2025 Mar;21(7):807-813. doi: 10.1080/14796694.2025.2461393. Epub 2025 Feb 6.
5
The higher initial dose and accelerated titration regimen of ropeginterferon as a treatment option for certain patients with polycythaemia vera.聚乙二醇干扰素的较高初始剂量和加速滴定方案作为真性红细胞增多症某些患者的一种治疗选择。
Br J Haematol. 2025 Mar;206(3):986-987. doi: 10.1111/bjh.19998. Epub 2025 Jan 12.
6
Molecular remission uncoupled with complete haematological response in polycythaemia vera treatment with ropeginterferon alfa-2b.在真性红细胞增多症患者接受聚乙二醇干扰素α-2b治疗过程中,分子学缓解与完全血液学缓解未同时出现。
Br J Haematol. 2024 Dec;205(6):2510-2514. doi: 10.1111/bjh.19846. Epub 2024 Oct 27.
7
Long-term safety and efficacy of ropeginterferon alfa-2b in Japanese patients with polycythemia vera.罗特西普干扰素 alfa-2b 在日本真性红细胞增多症患者中的长期安全性和疗效。
Int J Hematol. 2024 Dec;120(6):675-683. doi: 10.1007/s12185-024-03846-5. Epub 2024 Oct 3.
8
Combination therapy with ruxolitinib and pegylated interferon alfa-2a in newly diagnosed patients with polycythemia vera.芦可替尼联合聚乙二醇干扰素 α-2a 治疗初诊原发性骨髓纤维化患者。
Blood Adv. 2024 Oct 22;8(20):5416-5425. doi: 10.1182/bloodadvances.2024013170.
9
A randomized, double-blind, placebo-controlled phase 3 study to assess efficacy and safety of ropeginterferon alfa-2b in patients with early/lower-risk primary myelofibrosis.一项评估罗特西普干扰素 alfa-2b 在早期/低危原发性骨髓纤维化患者中的疗效和安全性的随机、双盲、安慰剂对照 3 期研究。
Ann Hematol. 2024 Sep;103(9):3573-3583. doi: 10.1007/s00277-024-05912-8. Epub 2024 Aug 15.
10
Treatment with ropeginterferon alfa-2b in patients with hydroxyurea resistant or intolerant polycythemia vera in South Korea: one-year results from a phase 2 study.韩国羟基脲耐药或不耐受真性红细胞增多症患者使用聚乙二醇干扰素α-2b治疗:一项2期研究的一年结果
Blood Res. 2024 Jul 9;59(1):23. doi: 10.1007/s44313-024-00026-6.

2025年亚洲骨髓增殖性肿瘤大会亮点:骨髓增殖性肿瘤分子发病机制与治疗策略的进展

Highlights from MPN Asia 2025: Advances in Molecular Pathogenesis and Therapeutic Strategies in Myeloproliferative Neoplasms.

作者信息

Bose Prithviraj, Xiao Zhijian, Hasselbalch Hans C, Prchal Josef T, Duan Minghui, Yacoub Abdulraheem, Rampal Raajit, Kiladjian Jean-Jacques, Hobbs Gabriela S, Tashi Tsewang, Shimoda Kazuya, Kirito Keita, Gill Harinder, Hou Hsin-An, Lee Sung-Eun, Huang Jian, Li Bing, Qin Albert, Yu Lennex Hsueh-Lin, Mascarenhas John O, Mesa Ruben A

机构信息

Department of Leukemia, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.

出版信息

Curr Hematol Malig Rep. 2025 Jul 12;20(1):9. doi: 10.1007/s11899-025-00752-3.

DOI:
10.1007/s11899-025-00752-3
PMID:40646417
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12254180/
Abstract

PURPOSE OF REVIEW

This report summarizes key insights from the 8th Annual International Symposium on Myeloproliferative Neoplasms (MPN Asia 2025). The symposium brought together global experts to discuss advancements in MPN biology, diagnostics, and therapeutics, with a focus on emerging molecular understanding, novel treatment strategies and real-world data.

RECENT FINDINGS

Molecular profiling has become essential in MPN risk stratification and therapeutic decision-making. High-risk mutations (e.g., ASXL1, TP53) and inflammatory pathways (e.g., IL-17, NF-κB) were shown to correlate with disease progression and transformation. Interferon-based therapy is increasingly used in younger, low-risk, or treatment-naïve patients, and is also being investigated in myelofibrosis and essential thrombocythemia. Ropeginterferon alfa-2b, a novel interferon-based therapy, demonstrated durable clinical efficacy in polycythemia vera. Its high initial-dose and accelerated titration (HIDAT) regimen led to fast achievement of complete hematologic response, rapid reductions in JAK2V617F allele burden, and high complete molecular response rate. Combination regimens involving ruxolitinib and agents such as pelabresib, selinexor, and interferon showed potential for enhanced efficacy. Population-based studies from Asia contributed regional epidemiological and treatment data, reinforcing the role of real-world evidence. Modern prognostic models such as MIPSS70+ v2.0 and GIPSS were discussed for more precise risk prediction. Preliminary findings also suggest ropeginterferon alfa-2b may be a safe option during pregnancy. MPN Asia 2025 highlighted the growing role of molecular diagnostics and targeted therapeutics in the management of MPNs. Ropeginterferon alfa-2b has emerged as a therapeutic potential across the MPN spectrum. Its early use and personalized strategies are increasingly recognized. Real-world data and regional insights are shaping a more nuanced, globally informed approach to MPN care.

摘要

综述目的

本报告总结了第八届骨髓增殖性肿瘤年度国际研讨会(MPN Asia 2025)的关键见解。该研讨会汇聚了全球专家,讨论骨髓增殖性肿瘤生物学、诊断和治疗方面的进展,重点关注新出现的分子认识、新型治疗策略和真实世界数据。

最新发现

分子谱分析在骨髓增殖性肿瘤风险分层和治疗决策中变得至关重要。高风险突变(如ASXL1、TP53)和炎症途径(如IL-17、NF-κB)与疾病进展和转化相关。基于干扰素的治疗越来越多地用于年轻、低风险或未接受过治疗的患者,并且也正在骨髓纤维化和原发性血小板增多症中进行研究。聚乙二醇化干扰素α-2b是一种新型的基于干扰素的治疗方法,在真性红细胞增多症中显示出持久的临床疗效。其高初始剂量和加速滴定(HIDAT)方案导致快速实现完全血液学缓解、JAK2V617F等位基因负担迅速降低以及高完全分子缓解率。涉及芦可替尼和诸如派拉布瑞西、塞利尼索和干扰素等药物的联合方案显示出增强疗效的潜力。来自亚洲的基于人群的研究提供了区域流行病学和治疗数据,加强了真实世界证据的作用。讨论了诸如MIPSS⁷⁰⁺ v2.0和GIPSS等现代预后模型以进行更精确的风险预测。初步研究结果还表明聚乙二醇化干扰素α-2b在怀孕期间可能是一种安全的选择。MPN Asia 2025强调了分子诊断和靶向治疗在骨髓增殖性肿瘤管理中日益重要的作用。聚乙二醇化干扰素α-2b已成为整个骨髓增殖性肿瘤谱系中的一种治疗潜力。其早期使用和个性化策略越来越受到认可。真实世界数据和区域见解正在塑造一种更细致入微、全球知情的骨髓增殖性肿瘤护理方法。