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Improved outcomes using tacrolimus/sirolimus for graft-versus-host disease prophylaxis with a reduced-intensity conditioning regimen for allogeneic hematopoietic cell transplant as treatment of myelofibrosis.采用他克莫司/西罗莫司预防移植物抗宿主病,联合强度降低的预处理方案进行异基因造血细胞移植治疗骨髓纤维化,可改善预后。
Biol Blood Marrow Transplant. 2010 Feb;16(2):281-6. doi: 10.1016/j.bbmt.2009.09.020. Epub 2009 Sep 26.
2
Prophylaxis with sirolimus and tacrolimus ± antithymocyte globulin reduces the risk of acute graft-versus-host disease without an overall survival benefit following allogeneic stem cell transplantation.西罗莫司和他克莫司联合抗胸腺细胞球蛋白预防可降低异基因造血干细胞移植后急性移植物抗宿主病的风险,但无总体生存获益。
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3
Comparison of Tacrolimus and Sirolimus (Tac/Sir) versus Tacrolimus, Sirolimus, and mini-methotrexate (Tac/Sir/MTX) as acute graft-versus-host disease prophylaxis after reduced-intensity conditioning allogeneic peripheral blood stem cell transplantation.他克莫司与西罗莫司(Tac/Sir)对比他克莫司、西罗莫司和小剂量甲氨蝶呤(Tac/Sir/MTX)用于减低剂量预处理异基因外周血干细胞移植后预防急性移植物抗宿主病的比较
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Graft-versus-host disease prophylaxis with tacrolimus and mycophenolate mofetil in HLA-matched nonmyeloablative transplant recipients is associated with very low incidence of GVHD and nonrelapse mortality.在人类白细胞抗原(HLA)匹配的非清髓性移植受者中,使用他克莫司和霉酚酸酯进行移植物抗宿主病(GVHD)预防,与GVHD和非复发死亡率的极低发生率相关。
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Leuk Lymphoma. 2015 Mar;56(3):663-70. doi: 10.3109/10428194.2014.930851. Epub 2014 Aug 6.
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[Study on graft-versus-host disease in the allogeneic peripheral blood stem cell transplantation for the treatment of leukemia].[异基因外周血干细胞移植治疗白血病的移植物抗宿主病研究]
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Outcome improvement over time in reduced intensity conditioning hematopoietic transplantation: a 20-year experience.随着时间的推移,在降低强度调理造血移植中改善结局:20 年的经验。
Ann Hematol. 2024 Jan;103(1):321-334. doi: 10.1007/s00277-023-05530-w. Epub 2023 Nov 16.
2
Results of a Phase II Trial of Allogeneic Hematopoietic Stem Cell Transplantation Using Y-Ibritumomab Tiuxetan (Zevalin) in Combination With Fludarabine and Melphalan in Patients With High-Risk B-Cell Non-Hodgkin's Lymphoma.异基因造血干细胞移植联合氟达拉滨和马法兰治疗高危 B 细胞非霍奇金淋巴瘤的 II 期临床试验结果。
Clin Lymphoma Myeloma Leuk. 2023 Sep;23(9):e268-e276. doi: 10.1016/j.clml.2023.05.011. Epub 2023 May 23.
3
Peritransplantation ruxolitinib administration is safe and effective in patients with myelofibrosis: a pilot open-label study.移植前使用鲁索替尼治疗骨髓纤维化患者是安全有效的:一项开放性Ⅰ期研究。
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2021 Update on allogeneic hematopoietic stem cell transplant for myelofibrosis: A review of current data and applications on risk stratification and management.2021 年异基因造血干细胞移植治疗骨髓纤维化的更新:当前数据在风险分层和管理方面的综述及应用。
Am J Hematol. 2021 Nov 1;96(11):1532-1538. doi: 10.1002/ajh.26349. Epub 2021 Oct 5.
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Long-Term Outcomes of Allogeneic Hematopoietic Cell Transplant with Fludarabine and Melphalan Conditioning and Tacrolimus/Sirolimus as Graft-versus-Host Disease Prophylaxis in Patients with Acute Lymphoblastic Leukemia.氟达拉滨和马法兰预处理、他克莫司/西罗莫司预防移植物抗宿主病的异基因造血细胞移植治疗急性淋巴细胞白血病患者的长期结局
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Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation From Unrelated Donor Using Tacrolimus/Sirolimus-based GvHD Prophylaxis: Impact of HLA Mismatch.异基因造血干细胞移植使用他克莫司/西罗莫司为基础的移植物抗宿主病预防方案的长期结果:HLA 错配的影响。
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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。
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10
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Leuk Suppl. 2012 May;1(Suppl 1):S2-7. doi: 10.1038/leusup.2012.2. Epub 2012 May 9.

本文引用的文献

1
A retrospective comparison of conventional intensity conditioning and reduced-intensity conditioning for allogeneic hematopoietic cell transplantation in myelofibrosis.骨髓纤维化患者异基因造血细胞移植中传统强度预处理与减低强度预处理的回顾性比较
Bone Marrow Transplant. 2009 Sep;44(5):317-20. doi: 10.1038/bmt.2009.10. Epub 2009 Feb 23.
2
JAK2-V617F-triggered preemptive and salvage adoptive immunotherapy with donor-lymphocyte infusion in patients with myelofibrosis after allogeneic stem cell transplantation.在异基因干细胞移植后的骨髓纤维化患者中,采用JAK2-V617F触发的先发制和挽救性过继性免疫疗法及供体淋巴细胞输注。
Blood. 2009 Feb 19;113(8):1866-8. doi: 10.1182/blood-2008-11-190975.
3
Treatment of myelofibrosis in younger patients: to transplant or not?年轻患者骨髓纤维化的治疗:是否进行移植?
Am J Hematol. 2009 Mar;84(3):131-2. doi: 10.1002/ajh.21368.
4
Conventional cytogenetics in myelofibrosis: literature review and discussion.骨髓纤维化中的传统细胞遗传学:文献综述与讨论
Eur J Haematol. 2009 May;82(5):329-38. doi: 10.1111/j.1600-0609.2009.01224.x. Epub 2009 Jan 9.
5
Graft-versus-host disease prophylaxis with everolimus and tacrolimus is associated with a high incidence of sinusoidal obstruction syndrome and microangiopathy: results of the EVTAC trial.依维莫司和他克莫司预防移植物抗宿主病与肝小静脉闭塞综合征和微血管病的高发生率相关:EVTAC试验结果
Biol Blood Marrow Transplant. 2009 Jan;15(1):101-8. doi: 10.1016/j.bbmt.2008.11.004.
6
New prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment.基于骨髓纤维化研究与治疗国际工作组的一项研究的原发性骨髓纤维化新预后评分系统。
Blood. 2009 Mar 26;113(13):2895-901. doi: 10.1182/blood-2008-07-170449. Epub 2008 Nov 6.
7
Allogeneic hematopoietic stem cell transplantation for myelofibrosis.异基因造血干细胞移植治疗骨髓纤维化
Haematologica. 2008 Oct;93(10):1449-50. doi: 10.3324/haematol.13801.
8
Sirolimus is associated with veno-occlusive disease of the liver after myeloablative allogeneic stem cell transplantation.西罗莫司与清髓性异基因干细胞移植后肝静脉闭塞性疾病有关。
Blood. 2008 Dec 1;112(12):4425-31. doi: 10.1182/blood-2008-07-169342. Epub 2008 Sep 5.
9
Allogeneic hematopoietic stem cell transplantation in myelofibrosis: the 20-year experience of the Gruppo Italiano Trapianto di Midollo Osseo (GITMO).骨髓纤维化中的异基因造血干细胞移植:意大利骨髓移植协作组(GITMO)的20年经验
Haematologica. 2008 Oct;93(10):1514-22. doi: 10.3324/haematol.12828. Epub 2008 Aug 25.
10
Relapse of postpolycythemia myelofibrosis after allogeneic stem cell transplantation in a polycythemic phase: successful treatment with donor lymphocyte infusion directed by quantitative PCR test for V617F-JAK2 mutation.真性红细胞增多症期异基因干细胞移植后真性红细胞增多症后骨髓纤维化复发:通过V617F-JAK2突变定量PCR检测指导的供体淋巴细胞输注成功治疗
Leukemia. 2008 Oct;22(10):1961-3. doi: 10.1038/leu.2008.215. Epub 2008 Aug 7.

采用他克莫司/西罗莫司预防移植物抗宿主病,联合强度降低的预处理方案进行异基因造血细胞移植治疗骨髓纤维化,可改善预后。

Improved outcomes using tacrolimus/sirolimus for graft-versus-host disease prophylaxis with a reduced-intensity conditioning regimen for allogeneic hematopoietic cell transplant as treatment of myelofibrosis.

机构信息

City of Hope Cancer Center, Department of Hematology/HCT, Duarte, California 91010, USA.

出版信息

Biol Blood Marrow Transplant. 2010 Feb;16(2):281-6. doi: 10.1016/j.bbmt.2009.09.020. Epub 2009 Sep 26.

DOI:10.1016/j.bbmt.2009.09.020
PMID:19786111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2819616/
Abstract

Allogeneic hematopoietic cell transplantation (HCT) using reduced-intensity conditioning (RIC) regimens is a potentially curative treatment for patients (patients) with myelofibrosis (MF), as we and others have reported. Nonrelapse mortality (NRM) from graft-versus-host disease (GVHD) and other complications has limited the success of this approach. As part of an ongoing prospective research study at City of Hope, a combination of tacrolimus/sirolimus +/- methotrexate (MTX) for GVHD prophylaxis has become the standard treatment for our allogeneic HCT patients. In this report, we present results for 23 consecutive patients, including extended follow up for 9 patients previously reported who received cyclosporine (CsA)/mycophenolate moffetil (MMF)+/-MTX, and the current series of 14 patients who received tacrolimus/sirolimus+/-MTX, and evaluate the impact of the GVHD prophylaxis regimen on the outcomes. Median follow-up for alive patients was 29.0 months (9.5-97.0). The estimated 2-year overall survival (OS) for the CsA/MMF cohort was 55.6% (confidence interval 36.0, 71.3), and for the tacrolimus/sirolimus cohort it was 92.9% (63.3, 98.8) (P=.047). The probability of grade III or IV acute GVHD (aGVHD) was 60% for the CsA/MMF patients, and 10% for the tacrolimus/sirolimus group (P=.0102). No significant differences were seen for grade II to IV aGVHD in the 2 groups. We conclude that the combination of tacrolimus/sirolimus+/-MTX for GVHD prophylaxis in the setting of RIC HCT for MF appears to reduce the incidence of severe aGVHD and NRM, and leads to improved OS compared to CSA/MMF+/-MTX.

摘要

异基因造血细胞移植(HCT)使用强度降低的调理(RIC)方案是治疗骨髓纤维化(MF)患者的潜在治愈性治疗方法,正如我们和其他人所报道的那样。移植物抗宿主病(GVHD)和其他并发症导致的非复发死亡率(NRM)限制了这种方法的成功。作为希望之城正在进行的前瞻性研究的一部分,他克莫司/西罗莫司 +/-甲氨蝶呤(MTX)联合用于 GVHD 预防已成为我们异基因 HCT 患者的标准治疗方法。在本报告中,我们报告了 23 例连续患者的结果,其中包括之前接受环孢素(CsA)/霉酚酸酯(MMF)+/-MTX 治疗的 9 例患者的扩展随访,以及当前系列的 14 例接受他克莫司/西罗莫司+/-MTX 治疗的患者,并评估了 GVHD 预防方案对结果的影响。存活患者的中位随访时间为 29.0 个月(9.5-97.0)。CsA/MMF 队列的 2 年总生存率(OS)估计为 55.6%(置信区间 36.0,71.3),而他克莫司/西罗莫司队列为 92.9%(63.3,98.8)(P=.047)。CsA/MMF 患者的 3 级或 4 级急性 GVHD(aGVHD)概率为 60%,而他克莫司/西罗莫司组为 10%(P=.0102)。两组间 2 级至 4 级 aGVHD 无显著差异。我们得出结论,RIC HCT 治疗 MF 时,他克莫司/西罗莫司+/-MTX 联合用于 GVHD 预防似乎可降低严重 aGVHD 和 NRM 的发生率,并导致 OS 改善,优于 CSA/MMF+/-MTX。