Real-World Outcomes of Allogeneic Stem Cell Transplantation in Relapsed Hodgkin Lymphoma: A Single-Center Experience from India.

Blood cell therapy Pub Date : 2026-02-13 eCollection Date: 2026-02-25 DOI:10.31547/bct-2025-018
Sarthak Wadhera, Rudra Narayan Swain, Aarushi Sahni, Charanpreet Singh, Aditya Jandial, Arihant Jain, Man Updesh Sachdeva, Rekha Hans, Deepesh Lad, Gaurav Prakash, Pankaj Malhotra, Alka Khadwal
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Abstract

Background: Relapsed Hodgkin lymphoma (HL) after autologous stem cell transplantation (auto-HSCT) remains a major therapeutic challenge with few curative options. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) may provide durable disease control, yet outcome data from tertiary-care centres in India are limited.

Objective: To evaluate real-world outcomes of allo-HSCT in patients with chemotherapy-sensitive relapsed HL at a tertiary care centre in North India.

Methods: This retrospective study included patients with chemotherapy-sensitive relapsed HL who underwent allo-HSCT at the Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, between January 2017 and December 2023. Clinical data including baseline characteristics, transplant parameters, complications, and survival outcomes were reviewed. Descriptive statistics were used, and overall survival (OS) was estimated using the Kaplan-Meier method.

Results: Five patients (median age 18 years; range 14-30) with chemotherapy-sensitive relapse following auto-HSCT underwent allogeneic transplantation in complete remission (CR) after salvage therapy. Donors included haploidentical (n=3), matched unrelated (n=1), and matched sibling (n=1). Four patients received reduced-intensity conditioning; one received myeloablative conditioning. Graft-versus-host disease (GVHD) prophylaxis included post-transplant cyclophosphamide (PT-Cy) in four patients. Neutrophil and platelet engraftment occurred at median 15 and 16 days, respectively. All patients developed bacterial infections; one succumbed to Gram-negative sepsis. Acute grade III GVHD occurred in one patient, and two developed limited chronic GVHD. At a median follow-up of 44 months, four patients remained in continuous remission, with a 3-year OS of 80%.

Conclusion: In Indian patients with chemotherapy-sensitive relapsed HL, allo-HSCT using reduced-intensity and reduced toxicity conditioning regimens and post-transplant cyclophosphamide-based regimens has proven feasible and effective, yielding encouraging survival outcomes within routine clinical practice.

异基因干细胞移植治疗复发性霍奇金淋巴瘤的真实世界结果:来自印度的单中心经验。
背景:自体干细胞移植(auto-HSCT)后复发霍奇金淋巴瘤(HL)仍然是一个主要的治疗挑战,治疗方案很少。同种异体造血干细胞移植(allo-HSCT)可能提供持久的疾病控制,但来自印度三级保健中心的结果数据有限。目的:评估印度北部三级医疗中心对化疗敏感的复发HL患者进行同种异体造血干细胞移植的实际结果。方法:这项回顾性研究包括2017年1月至2023年12月在昌迪加尔医学教育与研究研究生研究所(PGIMER)接受同种异体造血干细胞移植的化疗敏感复发HL患者。临床资料包括基线特征、移植参数、并发症和生存结果进行了回顾。采用描述性统计,采用Kaplan-Meier法估计总生存期(OS)。结果:5例自体造血干细胞移植后化疗敏感复发的患者(中位年龄18岁,范围14-30岁)在补救性治疗后完全缓解(CR)接受了同种异体移植。捐赠者包括单倍体(n=3),配对的非亲属(n=1)和配对的兄弟姐妹(n=1)。4例患者接受低强度调节;一组接受清髓条件反射。4例患者的移植物抗宿主病(GVHD)预防包括移植后环磷酰胺(PT-Cy)。中性粒细胞和血小板植入分别发生在中位时间15天和16天。所有患者均出现细菌感染;一例死于革兰氏阴性败血症。1例发生急性III级GVHD, 2例发展为有限的慢性GVHD。在中位随访44个月时,4例患者持续缓解,3年生存率为80%。结论:在印度化疗敏感的复发HL患者中,采用低强度、低毒性调节方案和移植后以环磷酰胺为基础的方案的同种异体造血干细胞移植已被证明是可行和有效的,在常规临床实践中产生了令人鼓舞的生存结果。
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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