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在资源有限的国家开展异基因造血祖细胞移植服务:挑战与成果

Developing an Allogeneic Hematopoietic Progenitor Cell Transplant Service in a Resource-Limited Country: Challenges and Outcomes.

作者信息

Mahar Uzma R, Ahsan Bushra, Ahmad Usman, Bokhari Syed W

机构信息

Medical Oncology, Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, PAK.

出版信息

Cureus. 2023 Sep 7;15(9):e44818. doi: 10.7759/cureus.44818. eCollection 2023 Sep.

Abstract

Introduction Allogeneic stem cell transplant has curative potential for many hematological disorders. Building an allogeneic hematopoietic progenitor cell transplant (HPCT) unit requires huge investment, infrastructure, equipment, medical supplies, and training of health care professionals. The key objective of this study is to share our experience of developing an allogeneic HPCT service at our tertiary care cancer hospital in a low-middle-income country. In addition, this study presents the outcomes of the first 30 allogeneic HPCTs done at our center. Methods This retrospective observational study included adult patients 18 years old or older with hematological malignancies who underwent allogeneic HPCT between July 2019 and April 2023 at Shaukat Khanum Memorial Cancer Hospital and Research Centre. Result Of the 30 patients, 24 underwent matched sibling donor (MSD) transplants in which a myeloablative-conditioning regimen (MAC) was used in 19, and a reduced conditioning regimen (RIC) was used in one. Of the six haploidentical-related donor transplants, four received MAC, and two received RIC. The median recipient age at HPCT was 23 and 21 years for MSD and Haplo-related donor transplants, respectively. The median follow-up duration was 12 months (Range: 10 days - 33 months). The overall survival rate at one year was 71.3% among all allogeneic stem cell transplant patients, whereas the disease-free survival rate at one year was 63.7%. In the acute lymphoblastic leukemia group, the disease-free survival rate at one year post allograft was 51.5%, while in the acute myeloid leukemia group, it was 78.7%. Conclusion This study demonstrates the successful development of an allogeneic bone marrow transplant unit at our hospital despite significant financial constraints. This has allowed us to provide a potentially curative and life-saving treatment to a substantial number of cancer patients. The bone marrow transplant outcomes of this study are comparable to those reported by international bone marrow transplant registries.

摘要

引言 异基因干细胞移植对许多血液系统疾病具有治愈潜力。建立一个异基因造血祖细胞移植(HPCT)单元需要巨额投资、基础设施、设备、医疗用品以及对医护人员的培训。本研究的关键目标是分享我们在一个中低收入国家的三级癌症医院开展异基因HPCT服务的经验。此外,本研究还展示了我们中心完成的前30例异基因HPCT的结果。

方法 这项回顾性观察研究纳入了2019年7月至2023年4月在沙卡特·汗姆纪念癌症医院和研究中心接受异基因HPCT的18岁及以上血液系统恶性肿瘤成年患者。

结果 在这30例患者中,24例接受了同胞全相合供者(MSD)移植,其中19例采用了清髓性预处理方案(MAC),1例采用了减低预处理方案(RIC)。在6例单倍体相关供者移植中,4例接受了MAC,2例接受了RIC。HPCT时MSD和单倍体相关供者移植的受者中位年龄分别为23岁和21岁。中位随访时间为12个月(范围:10天 - 33个月)。所有异基因干细胞移植患者的一年总生存率为71.3%,而一年无病生存率为6%. 在急性淋巴细胞白血病组,移植后一年的无病生存率为51.5%,而在急性髓细胞白血病组为78.7%。

结论 本研究表明,尽管存在重大资金限制,我们医院的异基因骨髓移植单元仍成功建立。这使我们能够为大量癌症患者提供潜在的治愈性和挽救生命的治疗。本研究的骨髓移植结果与国际骨髓移植登记处报告的结果相当。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81f2/10559081/ca4fa669c30e/cureus-0015-00000044818-i01.jpg

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