• 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
Hematopoietic Cell Transplantation for Myelofibrosis: the Dynamic International Prognostic Scoring System Plus Risk Predicts Post-Transplant Outcomes.造血细胞移植治疗骨髓纤维化:动态国际预后评分系统加风险预测移植后结局。
Biol Blood Marrow Transplant. 2018 Feb;24(2):386-392. doi: 10.1016/j.bbmt.2017.09.016. Epub 2017 Sep 29.
2
Allogeneic Transplantation for Patients With Advanced Myelofibrosis: Splenomegaly and High Serum LDH are Adverse Risk Factors for Successful Engraftment.晚期骨髓纤维化患者的异基因移植:脾肿大和高血清乳酸脱氢酶是成功植入的不良风险因素。
Clin Lymphoma Myeloma Leuk. 2016 May;16(5):297-303. doi: 10.1016/j.clml.2016.02.004. Epub 2016 Feb 18.
3
Dynamic International Prognostic Scoring System scores, pre-transplant therapy and chronic graft-versus-host disease determine outcome after allogeneic hematopoietic stem cell transplantation for myelofibrosis.动态国际预后评分系统评分、移植前治疗和慢性移植物抗宿主病决定了异基因造血干细胞移植治疗骨髓纤维化的预后。
Haematologica. 2012 Oct;97(10):1574-81. doi: 10.3324/haematol.2011.061168. Epub 2012 Apr 4.
4
The Dynamic International Prognostic Scoring System for myelofibrosis predicts outcomes after hematopoietic cell transplantation.动态国际预后评分系统对骨髓纤维化造血细胞移植后的结果具有预测作用。
Blood. 2012 Mar 15;119(11):2657-64. doi: 10.1182/blood-2011-08-372904. Epub 2012 Jan 10.
5
Survival following allogeneic transplant in patients with myelofibrosis.异基因移植后骨髓纤维化患者的生存情况。
Blood Adv. 2020 May 12;4(9):1965-1973. doi: 10.1182/bloodadvances.2019001084.
6
Prognostic risk models for transplant decision-making in myelofibrosis.骨髓纤维化移植决策的预后风险模型
Ann Hematol. 2018 May;97(5):813-820. doi: 10.1007/s00277-018-3240-x. Epub 2018 Jan 25.
7
MIPSS70+ v2.0 predicts long-term survival in myelofibrosis after allogeneic HCT with the Flu/Mel conditioning regimen.MIPSS70+ v2.0 预测 Flu/Mel 预处理方案异基因造血干细胞移植后骨髓纤维化的长期生存。
Blood Adv. 2019 Jan 8;3(1):83-95. doi: 10.1182/bloodadvances.2018026658.
8
Targeted Sequencing Improves DIPSS-Plus Prognostic Scoring in Myelofibrosis Patients Undergoing Allogeneic Transplantation.靶向测序可改善接受异基因移植的骨髓纤维化患者的 DIPSS-Plus 预后评分。
Biol Blood Marrow Transplant. 2020 Jul;26(7):1371-1374. doi: 10.1016/j.bbmt.2020.03.007. Epub 2020 Mar 16.
9
Comparison of Dynamic International Prognostic Scoring System and MYelofibrosis SECondary to PV and ET Prognostic Model for Prediction of Outcome in Polycythemia Vera and Essential Thrombocythemia Myelofibrosis after Allogeneic Stem Cell Transplantation.动态国际预后评分系统与原发性骨髓纤维化继发于 PV 和 ET 预后模型在异基因造血干细胞移植后对真性红细胞增多症和原发性血小板增多症骨髓纤维化结局预测的比较。
Biol Blood Marrow Transplant. 2019 Jun;25(6):e204-e208. doi: 10.1016/j.bbmt.2019.03.024. Epub 2019 Mar 28.
10
Allogeneic hematopoietic stem cell transplant overcomes the adverse survival effect of very high risk and unfavorable karyotype in myelofibrosis.异基因造血干细胞移植可克服骨髓纤维化中极高风险和不良核型的不良生存影响。
Am J Hematol. 2018 May;93(5):649-654. doi: 10.1002/ajh.25053. Epub 2018 Feb 24.

引用本文的文献

1
Role of molecular alterations in transplantation decisions for patients with primary myelofibrosis.分子改变在原发性骨髓纤维化患者移植决策中的作用
Blood Adv. 2025 Feb 25;9(4):797-807. doi: 10.1182/bloodadvances.2024014368.
2
Combination of ligand‑based and structure‑based virtual screening for the discovery of novel Janus kinase 2 inhibitors against philadelphia-negative myeloproliferative neoplasms.基于配体和基于结构的虚拟筛选相结合以发现针对费城阴性骨髓增殖性肿瘤的新型 Janus 激酶 2 抑制剂
Mol Divers. 2024 Aug 29. doi: 10.1007/s11030-024-10938-1.
3
Myelofibrosis and allogeneic transplantation: critical points and challenges.骨髓纤维化与异基因移植:关键点与挑战
Front Oncol. 2024 Jun 20;14:1396435. doi: 10.3389/fonc.2024.1396435. eCollection 2024.
4
Anti-T-lymphocyte globulin improves GvHD-free and relapse-free survival in myelofibrosis after matched related or unrelated donor transplantation.抗 T 淋巴细胞球蛋白可改善亲缘或非亲缘供者移植后骨髓纤维化患者的无移植物抗宿主病和无复发存活率。
Bone Marrow Transplant. 2024 Aug;59(8):1154-1160. doi: 10.1038/s41409-024-02291-6. Epub 2024 May 21.
5
A Review About the Assessment of the Bleeding and Thrombosis Risk for Patients With Myeloproliferative Neoplasms Scheduled for Surgery.关于计划接受手术的骨髓增殖性肿瘤患者出血和血栓形成风险评估的综述
Cureus. 2024 Mar 12;16(3):e56008. doi: 10.7759/cureus.56008. eCollection 2024 Mar.
6
Graft-versus-host disease and impact on relapse in myelofibrosis undergoing hematopoietic stem cell transplantation.移植物抗宿主病及其对骨髓纤维化造血干细胞移植后复发的影响。
Bone Marrow Transplant. 2024 Apr;59(4):550-557. doi: 10.1038/s41409-024-02220-7. Epub 2024 Feb 6.
7
JAK2 V617F mutation and associated chromosomal alterations in primary and secondary myelofibrosis and post-HCT outcomes.原发性和继发性骨髓纤维化及移植后 JAK2 V617F 突变和相关染色体改变的结果。
Blood Adv. 2023 Dec 26;7(24):7506-7515. doi: 10.1182/bloodadvances.2023010882.
8
JAK2 inhibitors for the treatment of Philadelphia-negative myeloproliferative neoplasms: current status and future directions.用于治疗费城染色体阴性骨髓增殖性肿瘤的JAK2抑制剂:现状与未来方向
Mol Divers. 2024 Oct;28(5):3445-3456. doi: 10.1007/s11030-023-10742-3. Epub 2023 Nov 25.
9
Allogeneic haematopoietic stem cell transplantation for myelofibrosis: prognostic indicators and the role of JAK2V617F measurable-residual disease monitoring by droplet-digital polymerase chain reaction.异基因造血干细胞移植治疗骨髓纤维化:预后指标和 JAK2V617F 检测的作用,采用液滴数字聚合酶链反应技术进行微量残留病灶监测。
Ann Hematol. 2023 Sep;102(9):2517-2527. doi: 10.1007/s00277-023-05312-4. Epub 2023 Jun 17.
10
A simple prognostic system in patients with myelofibrosis undergoing allogeneic stem cell transplantation: a CIBMTR/EBMT analysis.异基因造血干细胞移植治疗骨髓纤维化患者的简单预后系统:CIBMTR/EBMT 分析。
Blood Adv. 2023 Aug 8;7(15):3993-4002. doi: 10.1182/bloodadvances.2023009886.

本文引用的文献

1
Myeloablative Versus Reduced-Intensity Hematopoietic Cell Transplantation for Acute Myeloid Leukemia and Myelodysplastic Syndromes.急性髓系白血病和骨髓增生异常综合征的清髓性与减低强度造血细胞移植
J Clin Oncol. 2017 Apr 10;35(11):1154-1161. doi: 10.1200/JCO.2016.70.7091. Epub 2017 Feb 13.
2
The effect of long-term ruxolitinib treatment on JAK2p.V617F allele burden in patients with myelofibrosis.长期鲁索替尼治疗对骨髓纤维化患者JAK2p.V617F等位基因负荷的影响。
Blood. 2015 Sep 24;126(13):1551-4. doi: 10.1182/blood-2015-03-635235. Epub 2015 Jul 30.
3
Impact of allogeneic stem cell transplantation on survival of patients less than 65 years of age with primary myelofibrosis.异基因干细胞移植对年龄小于65岁的原发性骨髓纤维化患者生存的影响。
Blood. 2015 May 21;125(21):3347-50; quiz 3364. doi: 10.1182/blood-2014-10-608315. Epub 2015 Mar 17.
4
CALR vs JAK2 vs MPL-mutated or triple-negative myelofibrosis: clinical, cytogenetic and molecular comparisons.CALR 突变与 JAK2 突变、MPL 突变或三阴性骨髓纤维化的临床、细胞遗传学和分子比较。
Leukemia. 2014 Jul;28(7):1472-7. doi: 10.1038/leu.2014.3. Epub 2014 Jan 9.
5
How I assess comorbidities before hematopoietic cell transplantation.我如何在造血细胞移植前评估合并症。
Blood. 2013 Apr 11;121(15):2854-63. doi: 10.1182/blood-2012-09-455063. Epub 2013 Jan 25.
6
Dynamic International Prognostic Scoring System scores, pre-transplant therapy and chronic graft-versus-host disease determine outcome after allogeneic hematopoietic stem cell transplantation for myelofibrosis.动态国际预后评分系统评分、移植前治疗和慢性移植物抗宿主病决定了异基因造血干细胞移植治疗骨髓纤维化的预后。
Haematologica. 2012 Oct;97(10):1574-81. doi: 10.3324/haematol.2011.061168. Epub 2012 Apr 4.
7
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.
8
JAK inhibition with ruxolitinib versus best available therapy for myelofibrosis.芦可替尼与最佳可用疗法治疗骨髓纤维化的 JAK 抑制作用比较。
N Engl J Med. 2012 Mar 1;366(9):787-98. doi: 10.1056/NEJMoa1110556.
9
The Dynamic International Prognostic Scoring System for myelofibrosis predicts outcomes after hematopoietic cell transplantation.动态国际预后评分系统对骨髓纤维化造血细胞移植后的结果具有预测作用。
Blood. 2012 Mar 15;119(11):2657-64. doi: 10.1182/blood-2011-08-372904. Epub 2012 Jan 10.
10
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。
J Clin Oncol. 2011 Feb 1;29(4):392-7. doi: 10.1200/JCO.2010.32.2446. Epub 2010 Dec 13.

造血细胞移植治疗骨髓纤维化:动态国际预后评分系统加风险预测移植后结局。

Hematopoietic Cell Transplantation for Myelofibrosis: the Dynamic International Prognostic Scoring System Plus Risk Predicts Post-Transplant Outcomes.

机构信息

Fred Hutchinson Cancer Research Center, the University of Washington Medical Center/Seattle Cancer Care Alliance, Seattle, Washington.

Fred Hutchinson Cancer Research Center, the University of Washington Medical Center/Seattle Cancer Care Alliance, Seattle, Washington.

出版信息

Biol Blood Marrow Transplant. 2018 Feb;24(2):386-392. doi: 10.1016/j.bbmt.2017.09.016. Epub 2017 Sep 29.

DOI:10.1016/j.bbmt.2017.09.016
PMID:28970176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6481667/
Abstract

Hematopoietic cell transplantation (HCT) provides potentially curative treatment for patients with myelofibrosis (MF). HCT outcomes are associated with the Dynamic International Prognostic Scoring System (DIPSS) risk scores. In the present study we analyzed results in 233 patients to determine if the DIPSS plus classification, which adds cytogenetics, thrombocytopenia, and RBC transfusion dependence as risk factors, would better predict post-HCT outcomes than the original DIPSS. Multivariate analysis showed that each risk parameter incorporated into the DIPPS plus model contributed to its predictive power of overall mortality, relapse-free survival, and nonrelapse mortality. The 5-year overall survival (OS), relapse, and treatment-related mortality (TRM) rates for patients with low/intermediate-1 risk MF were 78%, 5%, and 20%, respectively. The 5-year OS, relapse, and TRM rates for patients with high-risk MF were 35%, 28%, and 40%, respectively. The HCT-specific comorbidity index of 3 or greater was associated with higher nonrelapse and overall mortality and reduced relapse-free survival. The relapse incidence was significantly increased in older patients (HR, 3.02; P = .0007). With a median follow-up of 8 years 124 patients (53%) were surviving. The components of the DIPSS plus classification still have prognostic relevance after adjustment by the DIPSS classification. This information should enhance our ability to advise patients when making decisions regarding timing of transplant.

摘要

造血细胞移植 (HCT) 为骨髓纤维化 (MF) 患者提供了潜在的治愈治疗方法。HCT 的结果与动态国际预后评分系统 (DIPSS) 风险评分相关。在本研究中,我们分析了 233 例患者的结果,以确定是否添加细胞遗传学、血小板减少症和红细胞输血依赖作为危险因素的 DIPSS 加分类可以比原始 DIPSS 更好地预测 HCT 后结局。多变量分析表明,DIPSS 加模型中纳入的每个风险参数都有助于其预测总死亡率、无复发生存率和非复发生存率的能力。低/中-1 风险 MF 患者的 5 年总生存率 (OS)、复发率和治疗相关死亡率 (TRM) 分别为 78%、5%和 20%。高危 MF 患者的 5 年 OS、复发率和 TRM 率分别为 35%、28%和 40%。HCT 特异性合并症指数为 3 或更高与非复发性和总死亡率较高以及无复发生存率降低相关。年龄较大的患者复发发生率显著增加(HR,3.02;P = .0007)。中位随访 8 年后,有 124 例患者(53%)存活。在 DIPSS 分类调整后,DIPSS 加分类的成分仍然具有预后意义。这些信息应该增强我们在决定移植时机时为患者提供建议的能力。