单倍体干细胞移植治疗新诊断的高危神经母细胞瘤:来自印度的单臂前瞻性研究结果

IF 0.9 4区 医学 Q4 ONCOLOGY
Indian journal of cancer Pub Date : 2025-01-01 Epub Date: 2025-05-16 DOI:10.4103/ijc.ijc_999_21
Venkateswaran V Swaminathan, Ramya Uppuluri, Satish K Meena, Harika Varla, Rumesh Chandar, Revathi Raj
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引用次数: 0

摘要

背景:随着神经母细胞瘤中移植物抗肿瘤(GVT)效应的数据越来越多,我们旨在评估单倍体干细胞移植(HSCT)作为一种诱导GVT的技术的可能性,从而改善高危神经母细胞瘤的预后。患者和方法:我们进行了一项前瞻性单臂研究,纳入了18个月至18岁的被诊断为高风险神经母细胞瘤的儿童,这些儿童接受了来自父母供体的单倍体造血干细胞移植。根据siop - europa - neuro母细胞瘤(SIOPEN)方案,所有儿童开始接受诱导化疗,然后进行评估和可行的手术。未经处理的移植物调节包括硫替帕/氟达拉滨/丁硫凡。对于t -缺失的移植物,调理包括兔抗胸腺细胞球蛋白/氟达拉滨/硫替帕/美伐兰。结果:在5名儿童中,1名儿童接受t -耗尽治疗,4名儿童接受移植后环磷酰胺的t -充满干细胞治疗,移植率100%,无方案相关毒性,并记录缓解。I/II级皮肤GVHD发生在所有对类固醇有反应的儿童中。我们对4名hsct后D + 60-75左右的儿童进行了累及野放疗,随后给予13-顺式维甲酸。移植后1年,3例发生孤立性中枢神经系统复发;1例患儿出现孤立性骨盆骨复发。1例患儿在移植后2个月复发。无进展生存期4/5例为12个月,1例为6个月。除一名儿童外,所有儿童复发后均因疾病进展而死亡。结论:在我们的队列中,高危神经母细胞瘤患儿在hsct后一年内持续复发。单倍体HSCT没有显示出显著的改善结果。我们迫切需要新的策略,包括通过前期metaiodobenzylguanidine (MIBG)治疗和HSCT进行更深层次的缓解诱导来改善结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Haploidentical stem cell transplantation in newly diagnosed high-risk neuroblastoma: Results from a single-arm, prospective study from India.

Background: With increasing data on graft-versus-tumor (GVT) effect in neuroblastoma, we aimed to evaluate the possibility of haploidentical stem cell transplantation (HSCT) as a technique to induce GVT and thereby improve outcomes in high-risk neuroblastoma.

Patients and methods: We performed a prospective, single-arm study and included children from 18 months to 18 years of age diagnosed with high-risk neuroblastoma and who underwent a haploidentical HSCT from a parent donor. All children were started on induction chemotherapy as per the SIOP-Europa-Neuroblastoma (SIOPEN) protocol, followed by assessment and surgery when feasible. Conditioning in the unmanipulated graft included thiotepa/fludarabine/busulfan. With a T-depleted graft, conditioning included rabbit anti-thymocyte globulin/fludarabine/thiotepa/melphalan.

Results: Of the five children, one child received T-depleted and four children received T-replete stem cells with posttransplant cyclophosphamide, with 100% engraftment, no regimen-related toxicities, and documented remission. Grade I/II skin GVHD occurred in all children who responded to steroids. We administered involved-field radiotherapy in four children around D + 60-75 post-HSCT, followed by 13-cis retinoic acid. At 1 year post-HSCT, three had isolated central nervous system relapse; one child had isolated pelvic bone relapse. One child relapsed 2 months post-HSCT. Progression-free survival was 12 months in 4/5 children and 6 months in one child. All except one child succumbed to progressive disease post relapse.

Conclusion: Children with high-risk neuroblastoma continued to relapse within a year post-HSCT in our cohort. Significant improvement in outcomes was not demonstrated with haploidentical HSCT. We urgently need new strategies including deeper remission induction with upfront metaiodobenzylguanidine (MIBG) therapy followed by HSCT to improve the outcomes.

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来源期刊
Indian journal of cancer
Indian journal of cancer Medicine-Oncology
CiteScore
1.40
自引率
0.00%
发文量
67
审稿时长
>12 weeks
期刊介绍: Indian Journal of Cancer (ISSN 0019-509X), the show window of the progress of ontological sciences in India, was established in 1963. Indian Journal of Cancer is the first and only periodical serving the needs of all the specialties of oncology in India.
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