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一名接受异基因非亲属移植后复发的霍奇金淋巴瘤患者使用纳武单抗治疗后发生耐药性移植物抗宿主病

Development of Resistant GvHD in a Patient Treated with Nivolumab for Hodgkins Lymphoma Relapse after Allogeneic Unrelated Transplantation.

作者信息

Steinerová K, Jindra P, Lysák D, Karas M

出版信息

Klin Onkol. 2019 Winter;32(1):66-69. doi: 10.14735/amko2019.

Abstract

BACKGROUND

Allogeneic hematopoietic stem cell transplantation is one of the therapeutic options for patients with relapsed or refractory classic Hodgkins lymphoma (cHL). In the case of dis-ease relapse after transplant, other treatment options are still limited (for example donor lymphocyte infusion, and chemother-apy with brentuximab, bendamustine, or other agents) with uncertain outcomes in terms of patient tolerance and long-term dis-ease remission. One way to achieve remission is administration of the PD-1 inhibitor nivolumab, a PD-1 checkpoint inhibitor. Nivolumab is also indicated for the treatment of cHL relapses after autologous hematopoietic stem cell transplantation. Since September 2018, nivolumab has been approved by the State Institute for Drug Control in the Czech Republic for treatment of cHL autologous hematopoietic stem cell transplantation relapse; however, treatment with nivolumab is accompanied by an increased risk of develop-ing fatal, acute graft-versus-host dis-ease.

CASE

The article describes the development of resistant acute graft-versus-host disease in a patient who had received allogeneic-unrelated transplantation and nivolumab treatment for Hodgkins lymphoma relapse.

CONCLUSION

Our case study, as well as the literature review, demonstrates the excellent efficacy of PD-1 inhibitors, but also cautions against the administration of these agents in patients follow-ing allogeneic hematopoietic stem cell transplantation. Administration of nivolumab to these patients should be done on a strictly individual basis in the context of known risks, and consideration should be given to other treatment options. Key words Hodgkins lymphoma -  PD-1 inhibitor -  nivolumab -  GvHD -  transplantation.

摘要

背景

异基因造血干细胞移植是复发或难治性经典霍奇金淋巴瘤(cHL)患者的治疗选择之一。移植后疾病复发时,其他治疗选择仍然有限(例如供体淋巴细胞输注,以及使用brentuximab、苯达莫司汀或其他药物进行化疗),在患者耐受性和长期疾病缓解方面的结果尚不确定。实现缓解的一种方法是给予PD-1抑制剂纳武单抗,一种PD-1检查点抑制剂。纳武单抗也适用于治疗自体造血干细胞移植后的cHL复发。自2018年9月以来,纳武单抗已被捷克共和国国家药物管制研究所批准用于治疗cHL自体造血干细胞移植复发;然而,使用纳武单抗治疗会增加发生致命性急性移植物抗宿主病的风险。

病例

本文描述了一名接受异基因无关移植和纳武单抗治疗霍奇金淋巴瘤复发患者发生耐药性急性移植物抗宿主病的情况。

结论

我们的病例研究以及文献综述表明,PD-1抑制剂具有出色的疗效,但也警示了在异基因造血干细胞移植后的患者中使用这些药物的风险。在已知风险的情况下,应严格根据个体情况对这些患者使用纳武单抗,并应考虑其他治疗选择。关键词 霍奇金淋巴瘤 - PD-1抑制剂 - 纳武单抗 - 移植物抗宿主病 - 移植

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