Non-cryopreserved autologous peripheral blood stem cell transplantation for multiple myeloma and lymphoma in countries with limited resources: practice considerations from the Worldwide Network for Blood and Marrow Transplantation

IF 4.5 2区 医学 Q1 HEMATOLOGY Bone Marrow Transplantation Pub Date : 2024-10-07 DOI:10.1038/s41409-024-02431-y
Mohamed Amine Bekadja, Dietger Niederwiser, Mohamed A. Kharfan-Dabaja, Riad El Fakih, Laurent Garderet, Ibrahim Yakoub-Agha, Hildegard Greinix, Daniel J. Weisdorf, Sebastian Galeano, Syed Osman Ahmed, Christian Chabanon, Shahrukh K. Hashmi, Annalisa Ruggeri, Usama Gergis, Ali Bazarbachi, Nada Hamad, Amal Albeihany, Marcelo Pasquini, Amr Hanbali, Jeff Szer, Yoshihisa Kodera, Ambuj Kumar, Tusneem Elhassan, Donal McLornan, Nina Worel, Raffaella Greco, Mohamad Mohty, Yoshiko Atsuta, Mickey Koh, Anna Sureda, Damiano Rondelli, Mahmoud Aljurf, Walid Rasheed
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Abstract

Autologous peripheral blood stem cell (PBSC) transplantation is a standard treatment of multiple myeloma (MM), Hodgkin lymphoma and various subtypes of non-Hodgkin lymphoma. Cryopreservation of hematopoietic stem cells is standard practice that allows time for delivery of conditioning regimen prior to cell infusion. The aim of this Worldwide Network for Blood & Marrow Transplantation (WBMT) work was to assess existing evidence on non-cryopreserved autologous transplants through a systematic review/meta-analysis, to study feasibility and safety of this approach. We searched PubMed, Web of Science and SCOPUS for studies that utilized non-cryopreserved autologous PBSC transplantation. Identified literature was reviewed for information on mobilization, apheresis, preservation and viability, conditioning regimen, engraftment, response, and survival. Results highlight collective experience from 19 transplant centers (1686 patients), that performed autologous transplants using non-cryopreserved PBSCs. The mean of infused CD34+ was 5.6 × 106/kg. Stem cell viability at transplantation was >90% in MM and >75% in lymphomas, after a storage time of 24–144 h at +4 °C. Mean time-to-neutrophil engraftment was 12 days and 15.3 days for platelets. Pooled proportion estimates of day 100 transplant-related mortality and graft failure were 1% and 0%, respectively. Non-cryopreservation of apheresed autologous PBSCs appears feasible and safe.

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在资源有限的国家进行非冷冻自体外周血干细胞移植治疗多发性骨髓瘤和淋巴瘤:全球血液和骨髓移植网络的实践考虑。
自体外周血干细胞(PBSC)移植是治疗多发性骨髓瘤(MM)、霍奇金淋巴瘤和各种亚型非霍奇金淋巴瘤的标准方法。低温保存造血干细胞是标准做法,可为细胞输注前的调理治疗留出时间。这项全球血液与骨髓移植网络(WBMT)工作的目的是通过系统回顾/元分析评估非冷冻自体移植的现有证据,研究这种方法的可行性和安全性。我们在 PubMed、Web of Science 和 SCOPUS 上搜索了利用非干细胞自体 PBSC 移植的研究。我们对识别出的文献进行了审查,以了解有关动员、分离、保存和存活、调理方案、移植、反应和存活的信息。结果强调了 19 个移植中心(1686 名患者)使用非干细胞保存的 PBSCs 进行自体移植的集体经验。输注的 CD34+ 平均值为 5.6 × 106/kg。干细胞在+4 °C储存24-144小时后,在MM中的移植存活率大于90%,在淋巴瘤中的移植存活率大于75%。中性粒细胞移植的平均时间为 12 天,血小板移植的平均时间为 15.3 天。第100天移植相关死亡率和移植失败的汇总比例估计分别为1%和0%。非冷冻保存非血清自体PBSCs似乎是可行和安全的。
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来源期刊
Bone Marrow Transplantation
Bone Marrow Transplantation 医学-免疫学
CiteScore
8.40
自引率
8.30%
发文量
337
审稿时长
6 months
期刊介绍: Bone Marrow Transplantation publishes high quality, peer reviewed original research that addresses all aspects of basic biology and clinical use of haemopoietic stem cell transplantation. The broad scope of the journal thus encompasses topics such as stem cell biology, e.g., kinetics and cytokine control, transplantation immunology e.g., HLA and matching techniques, translational research, and clinical results of specific transplant protocols. Bone Marrow Transplantation publishes 24 issues a year.
期刊最新文献
A formula using day 4 parameters to predict next-day peripheral blood stem cell yield in healthy haematopoietic stem cell donors. Significant detrimental impact of pre-transplant mogamulizumab on the post-transplant outcome with a short interval between the last mogamulizumab and transplantation. Treatment failure patterns in early versus late introduction of CAR T-cell therapy in large B-cell lymphoma. Enhanced antileukemic effect of NKp30b isoform of donor-derived NK cells infused after HLA-haploidentical allogeneic hematopoietic cell transplantation in high-risk AML and MDS. Dynamics of neoantigen-specific T-cells in post-transplant relapse: do leukemia neoantigens elicit immune responses in transplant recipients?
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