Improving outcomes of hematopoietic stem cell transplant for leukemia in children and young adults in resource-limited setting

Garima Nirmal , Subhashish Paul , Vaibhav Chadha , Shreyasi Das , Mohit Chaudhary , Manju Joseph , Bharti Sharma , Himshikha Yadav , K.K. Swathymon , Iskandarov Kamol , Gaurav Kharya
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Abstract

Introduction

Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative approach in patients with relapsed and high-risk leukemia. This retrospective analysis aimed to investigate outcomes and risk factors associated with HSCT in children and young adults with hematological malignancies in a resource-limited setting.

Methods

We retrospectively evaluated 48 pediatric and young adult patients diagnosed with hematological malignancies who underwent HSCT at our institution between April 2017 and Jan 2023.

Result

The median age of the cohort was 10 years (6 months - 21 years), and the majority of patients underwent transplants for acute lymphoblastic leukemia (ALL) (n = 24; 50 %) and acute myeloid leukemia (n = 18; 37.5%). Median time to neutrophil and platelet engraftment were 15 days (range 9–28) and 18 days (range 9–40), respectively. One patient had primary graft failure. Cytomegalovirus reactivation occurred in 21 patients (43.8%). Seventeen patients received escalated donor lymphocyte infusion (DLI). With a median follow-up of 902 days (52–2490), the probability of event free survival and overall survival (OS) was 65.9% and 69.4%. OS for lymphoid and myeloid malignancies were 64.7% and 75.2%, respectively. Kaplan-Meier probabilities of OS for patients in first complete remission (CR), CR2, CR3, or with refractory disease were 80%, 76.2%, 0%, and 40%, respectively (p = 0.02). OS of the patients undergoing matched sibling donor (n = 17) or haploidentical HSCT (n = 31) was 70.6% and 69%, respectively (p = 0.989).

Conclusions

Our study demonstrates excellent outcomes of patients with hematological malignancies undergoing allogeneic HSCT with similar outcomes in HLA-identical sibling donors and haploidentical first-degree family donors. Prophylactic DLI might be considered in patients with high-risk leukemia to prevent relapse, including ALL.

在资源有限的情况下改善儿童和青少年白血病造血干细胞移植的疗效
导言异基因造血干细胞移植(HSCT)是治疗复发和高危白血病患者的一种方法。这项回顾性分析旨在研究在资源有限的环境中,儿童和年轻成人血液恶性肿瘤患者接受造血干细胞移植的结果和相关风险因素。方法我们回顾性评估了2017年4月至2023年1月期间在我院接受造血干细胞移植的48名儿童和年轻成人血液恶性肿瘤患者。结果队列的中位年龄为10岁(6个月-21岁),大多数患者接受了急性淋巴细胞白血病(ALL)(n = 24;50%)和急性髓性白血病(n = 18;37.5%)的移植。中性粒细胞和血小板移植的中位时间分别为15天(9-28天)和18天(9-40天)。一名患者出现原发性移植失败。21名患者(43.8%)出现巨细胞病毒再激活。17名患者接受了升级的供体淋巴细胞输注(DLI)。中位随访时间为 902 天(52-2490 天),无事件生存率和总生存率(OS)分别为 65.9% 和 69.4%。淋巴恶性肿瘤和骨髓恶性肿瘤的OS分别为64.7%和75.2%。首次完全缓解(CR)、CR2、CR3 或难治性疾病患者的 OS 的 Kaplan-Meier 概率分别为 80%、76.2%、0% 和 40%(P = 0.02)。结论:我们的研究表明,接受异基因造血干细胞移植的血液恶性肿瘤患者疗效极佳,HLA相同的同胞供者和单倍体一级直系亲属供者的疗效相似。高危白血病(包括 ALL)患者可考虑预防性 DLI,以防止复发。
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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