干细胞移植治疗复发/难治性霍奇金淋巴瘤

Q4 Medicine
S. Stavrik, A. Sureda
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引用次数: 0

摘要

虽然大多数霍奇金淋巴瘤(HL)患者通过初始治疗治愈,但在85-90%的早期和70-80%的晚期疾病病例中,复发仍然是一个主要问题。挽救性化疗后的自体干细胞移植(auto-HCT)目前被认为是一线化疗后复发或一线治疗失败的患者的标准治疗方法。随着新的以药物为基础的挽救策略和auto-HCT后的巩固策略的引入,auto-HCT的治疗能力不断提高。同种异体干细胞移植(Allogeneic stem cell transplantation, allo-HCT)是一种合理的治疗选择,适用于自体干细胞移植后复发或进展的年轻患者,并且在移植时患有化疗敏感性疾病。Allo-HCT是复发/难治性HL (r/r HL)患者的有效治疗策略,因为随着时间的推移,结果有所改善,主要是Allo-HCT和新药的安全联合。考虑到单倍体干细胞移植(haploi - hct)的结果与匹配的兄弟姐妹供体和匹配的非亲属供体相当,对于没有供体的r/r HL患者或在没有匹配的亲属供体的情况下急需寻找供体的患者,haploi - hct现在是首选的替代供体来源。针对复发或难治性HL的抗cd30单克隆抗体和检查点抑制剂(CPI)等新药的开发已显示出高缓解率和持久缓解,并对HCT的作用和时间提出了挑战。同种异体hct治疗后出现疾病复发或进展的HL患者的治疗仍然是一个真正的挑战和未满足的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stem-Cell Transplantation in Adult Patients with Relapsed/Refractory Hodgkin Lymphoma
Although the majority of patients with Hodgkin lymphoma (HL) are cured with initial therapy, in 85–90% of early stage and 70–80% of advanced-stage disease cases, relapse remains a major problem. Autologous stem-cell transplantation (auto-HCT) after salvage chemotherapy is currently considered to be the standard of care for patients who relapse after first-line chemotherapy or for whom first-line treatment fails. The curative capacity of auto-HCT has been improving with the introduction of new drug-based salvage strategies and consolidation strategies after auto-HCT. Allogeneic stem-cell transplantation (allo-HCT) represents a reasonable treatment option for young patients who relapse or progress after auto-HCT and have chemosensitive disease at the time of transplantation. Allo-HCT is a valid treatment strategy for patients with relapse/refractory HL (r/r HL) because the results have improved over time, mainly with the safe combination of allo-HCT and new drugs. Bearing in mind that outcomes after haploidentical stem-cell transplantation (haplo-HCT) are comparable with those for matched sibling donors and matched unrelated donors, haplo-HCT is now the preferred alternative donor source for patients with r/r HL without a donor or when there is urgency to find a donor if a matched related donor is not present. The development of new drugs such as anti-CD 30 monoclonal antibodies and checkpoint inhibitors (CPI) for relapsed or refractory HL has demonstrated high response rates and durable remissions, and challenged the role and timing of HCT. The treatment of patients with HL who develop disease recurrence or progression after allo-HCT remains a real challenge and an unmet need.
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来源期刊
Cell and Organ Transplantology
Cell and Organ Transplantology Medicine-Transplantation
CiteScore
0.40
自引率
0.00%
发文量
8
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