A novel reduced toxicity conditioning regimen for older myelodysplastic neoplasms patients undergoing haploidentical stem cell transplantation: a prospective cohort study.

IF 3.6 3区 医学 Q2 ONCOLOGY
American journal of cancer research Pub Date : 2025-01-15 eCollection Date: 2025-01-01 DOI:10.62347/OFXJ3130
Wen-Jing Yu, Yu-Qian Sun, Xiao-Hui Zhang, Lan-Ping Xu, Xiao-Dong Mo, Meng Lv, Xiao-Jun Huang, Yu Wang
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引用次数: 0

Abstract

A novel reduced-toxicity conditioning (RTC) regimen of busulfan, fludarabine, cyclophosphamide, and antithymocyte globulin (Bu/Flu/Cy/ATG) followed by haploidentical hematopoietic stem cell transplantation (haplo-HSCT) in older patients with hematologic malignancies has been reported and the results was encouraging. However, the safety and efficacy of this regimen was unknown in older myelodysplastic neoplasms (MDS) patients. From January 2018 to December 2021, 68 consecutive older patients (aged over 50) using the RTC regimen for T-cell replete haplo-HSCT (RTC group) at our center were eligible, 68 patients aged under 50 using modified busulfan, cyclophosphamide plus antithymocyte globulin regimen (Bu/Cy/ATG) (Bu/Cy/ATG group) were randomly selected from 223 MDS patients during the same period in a 1:1 ratio matched-pair analysis for patient sex, World Health Organization (WHO) category, international prognostic scoring system (IPSS) risk group, time from diagnosis to HSCT, chemotherapy in advanced, response after chemotherapy, donor sex, infused mononuclear cells and the CD34-positive cell count. The transplant outcomes were also compared between the RTC group and the matched sibling donor (MSD) haploidentical stem cell transplantation (HSCT) with the busulfan and cyclophosphamide (Bu/Cy) conditioning regimen. The cumulative incidences of grade II-IV acute graft versus host disease (aGVHD) in the RTC group were significantly lower than that in the Bu/Cy/ATG group. The 3-year cumulative incidences of treatment related mortality (TRM) in the two groups were 12.3% versus 14.7% (P=0.613). The cumulative incidences of relapse, disease-free survival (DFS) and overall survival (OS) were comparable between the two groups. The outcomes were better in RTC group than those patients received MSD transplant, with lower incidence of TRM, and higher OS and DFS. The advantages were still significant when comparing patients receiving children donors HSCT in RTC group with MSD transplant in survival and TRM. Children donor with the RTC regimen could be a better choice than the MSD HSCT with Bu/Cy regimen for the elderly MDS patients. The encouraging results suggest that the RTC regimen followed by haplo-HSCT is a potentially promising method for older MDS patients. The trail number of the prospective study is "NCT03412409" and the trial URL is "https://clinicaltrials.gov/study/NCT03412409?term=NCT03412409&rank=1".

一种新的低毒性调节方案用于接受单倍体干细胞移植的老年骨髓增生异常肿瘤患者:一项前瞻性队列研究。
一种新的降低毒性调节(RTC)方案,由布苏丹、氟达拉滨、环磷酰胺和抗胸腺细胞球蛋白(Bu/Flu/Cy/ATG)治疗老年血液病恶性患者,随后进行单倍同型造血干细胞移植(haploi - hsct),结果令人鼓舞。然而,该方案在老年骨髓增生异常肿瘤(MDS)患者中的安全性和有效性尚不清楚。2018年1月至2021年12月,本中心采用RTC方案进行t细胞全单倍造血干细胞移植(RTC组)的连续老年患者68例(50岁以上),在同一时期从223例MDS患者中随机选择使用改良的布磺凡、环磷酰胺加抗胸腺细胞球蛋白方案(Bu/Cy/ATG组)的50岁以下患者68例(Bu/Cy/ATG组),按患者性别、世界卫生组织(WHO)类别进行1:1比例配对分析,国际预后评分系统(IPSS)风险组、诊断至HSCT时间、晚期化疗、化疗后反应、供者性别、输注单核细胞及cd34阳性细胞数。移植结果还比较了RTC组和配对兄弟姐妹供体(MSD)单倍体干细胞移植(HSCT)与busulfan和环磷酰胺(Bu/Cy)调节方案之间的移植结果。RTC组II-IV级急性移植物抗宿主病(aGVHD)的累积发生率显著低于Bu/Cy/ATG组。两组治疗相关死亡率(TRM)的3年累积发生率分别为12.3%和14.7% (P=0.613)。两组之间的累积复发发生率、无病生存期(DFS)和总生存期(OS)具有可比性。RTC组预后优于MSD组,TRM发生率较低,OS和DFS较高。当比较RTC组接受儿童供体HSCT和MSD移植的患者的生存和TRM时,优势仍然显着。对于老年MDS患者,儿童供体RTC方案可能比MSD HSCT + Bu/Cy方案更好。令人鼓舞的结果表明,RTC方案后单倍造血干细胞移植是一种潜在的有希望的老年MDS患者的方法。前瞻性研究的试验编号为“NCT03412409”,试验URL为“https://clinicaltrials.gov/study/NCT03412409?term=NCT03412409&rank=1”。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
3.80%
发文量
263
期刊介绍: The American Journal of Cancer Research (AJCR) (ISSN 2156-6976), is an independent open access, online only journal to facilitate rapid dissemination of novel discoveries in basic science and treatment of cancer. It was founded by a group of scientists for cancer research and clinical academic oncologists from around the world, who are devoted to the promotion and advancement of our understanding of the cancer and its treatment. The scope of AJCR is intended to encompass that of multi-disciplinary researchers from any scientific discipline where the primary focus of the research is to increase and integrate knowledge about etiology and molecular mechanisms of carcinogenesis with the ultimate aim of advancing the cure and prevention of this increasingly devastating disease. To achieve these aims AJCR will publish review articles, original articles and new techniques in cancer research and therapy. It will also publish hypothesis, case reports and letter to the editor. Unlike most other open access online journals, AJCR will keep most of the traditional features of paper print that we are all familiar with, such as continuous volume, issue numbers, as well as continuous page numbers to retain our comfortable familiarity towards an academic journal.
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