Kumar Rajiv, Kapoor Rajan, Sharma Sanjeevan, Pramanik Suman Kumar, Yanamandra Uday, Mishra Kundan, Khera Sanjeev, Sharma Ajay, Das S, Verma Tarun, Singh Jasjit, Nair Velu
Senior Advisor (Medicine) & Clinical Hematologist, Army Hospital (R&R), New Delhi, India.
Consultant (Medicine) & Clinical Hematologist, Army Hospital (R&R), New Delhi, India.
Med J Armed Forces India. 2023 Nov-Dec;79(6):657-664. doi: 10.1016/j.mjafi.2023.09.005. Epub 2023 Sep 13.
Bone Marrow Transplant (BMT) is a curative form of therapy for many hematological disorders in both the adult and pediatric patients. The availability of BMT in the AFMS at AHRR for the last 02 decades has been a game changer for the patients.
We reviewed our BMT data since the inception of the program till Feb 2023.
Over 700 patients with more than 23 different types of hematological disorders have undergone this procedure 58%% patients underwent an Autologous BMT and 42% an allogenic BMT. Autologous BMT for Multiple Myeloma and Allogenic BMT for Aplastic Anemia and Acute Leukemias have been the most common indications. 73% patients were adults, and 27% patients were of the pediatric age group. The male: female ratio was 2:1. The spectrum of allogenic Hematopoietic Stem Cell Transplant (HSCT) has expanded from Matched Sibling Donor (MSD) transplants to Matched Unrelated Donor (MUD) Transplants and Haploidentical Donor Transplants. 93% of our Allogenic BMT patients underwent a MSD BMT, 1% MUD BMT and 06% Haploidentical BMT. Today no patient with a malignant hematological disorder requiring a BMT is denied the procedure due to the lack of an HLA donor due to the availability of haploidentical BMT.
The evolution of a BMT program has a long learning curve and the expanded pool of eligible donors has led to a situation of "transplant for all". Haploidentical HSCT for nonmalignant hematological disorders is an unmet need. CART cell therapy and Cellular therapies need to be prioritized for future inclusion.
骨髓移植(BMT)是治疗成人和儿童多种血液系统疾病的一种治愈性疗法。在过去二十年里,AHRR的AFMS能够开展BMT,这对患者来说是一个改变局面的因素。
我们回顾了自该项目启动至2023年2月的BMT数据。
700多名患有23种以上不同类型血液系统疾病的患者接受了该手术,58%的患者接受了自体BMT,42%接受了同种异体BMT。多发性骨髓瘤的自体BMT以及再生障碍性贫血和急性白血病的同种异体BMT是最常见的适应症。73%的患者为成年人,27%为儿童年龄组。男女比例为2:1。同种异体造血干细胞移植(HSCT)的范围已从匹配同胞供体(MSD)移植扩大到匹配无关供体(MUD)移植和单倍体相合供体移植。我们93%的同种异体BMT患者接受了MSD BMT,1%接受了MUD BMT,6%接受了单倍体相合BMT。如今,由于有单倍体相合BMT,没有一名需要BMT的恶性血液系统疾病患者因缺乏HLA供体而无法接受该手术。
BMT项目的发展有一个漫长的学习曲线,合格供体库的扩大导致了“全民移植”的局面。非恶性血液系统疾病的单倍体相合HSCT是未得到满足的需求。CAR-T细胞疗法和细胞疗法需要在未来优先纳入。