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异基因干细胞移植后难治性霍奇金淋巴瘤采用低剂量纳武单抗治疗成功。

Successful treatment with low-dose nivolumab in refractory Hodgkin lymphoma after allogeneic stem cell transplantation.

作者信息

Onizuka Makoto, Kojima Minoru, Matsui Keiko, Machida Shinichiro, Toyosaki Masako, Aoyama Yasuyuki, Kawai Hidetsugu, Amaki Jun, Hara Ryujiro, Ichiki Akifumi, Ogawa Yoshiaki, Kawada Hiroshi, Nakamura Naoya, Ando Kiyoshi

机构信息

Department of Hematology and Oncology, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa, 259-1143, Japan.

Department of Hematology, Ebina General Hospital, Ebina, Kanagawa, Japan.

出版信息

Int J Hematol. 2017 Jul;106(1):141-145. doi: 10.1007/s12185-017-2181-9. Epub 2017 Jan 17.

Abstract

Previous studies have reported that an antibody that blocks programmed cell death 1 (PD-1) has therapeutic activity in patients with refractory/relapsed Hodgkin lymphoma (HL). However, the safety and efficacy of these agents in the post-allogeneic stem cell transplantation (allo-SCT) setting are not well known. Here, we describe a patient who was diagnosed as classical HL and treated with five regimens of chemotherapies with autologous SCT. Complete remission (CR) was not achieved following this initial treatment, so we performed allo-SCT from an HLA-matched sibling donor. Since his disease progressed at day 403 after allo-SCT, we decided to use nivolumab in the treatment of his refractory disease. To prevent the worsening of his chronic graft-versus-host disease (GVHD), we reduced the initial dose and frequency of nivolumab compared with the previous report. After four courses of 0.5 mg/kg of nivolumab every three weeks, FDG-PET imaging showed partial response (PR) to the treatment, a remarkable result. However, since the escalated dose of 2 mg/kg resulted in worsening of dyspnea and skin sclerosis, we initiated systemic administration of prednisolone and reduced nivolumab to 1 mg/kg. At the time of this report, his HL is in stable PR with three weekly administration of nivolumab and steroid controlled mild chronic GVHD.

摘要

既往研究报道,一种阻断程序性细胞死亡1(PD-1)的抗体对难治性/复发性霍奇金淋巴瘤(HL)患者具有治疗活性。然而,这些药物在异基因造血干细胞移植(allo-SCT)后的安全性和疗效尚不清楚。在此,我们描述了一名被诊断为经典型HL的患者,其接受了五种化疗方案及自体SCT治疗。初始治疗后未达到完全缓解(CR),因此我们对其进行了来自HLA匹配同胞供者的allo-SCT。由于其疾病在allo-SCT后第403天进展,我们决定使用纳武单抗治疗其难治性疾病。为防止其慢性移植物抗宿主病(GVHD)恶化,与既往报道相比,我们降低了纳武单抗的初始剂量和给药频率。每三周给予0.5mg/kg纳武单抗四个疗程后,FDG-PET成像显示治疗有部分缓解(PR),这是一个显著的结果。然而,由于将剂量增至2mg/kg导致呼吸困难和皮肤硬化加重,我们开始全身给予泼尼松龙,并将纳武单抗剂量减至1mg/kg。在本报告撰写之时,其HL处于稳定的PR状态,每三周给予一次纳武单抗,且类固醇控制着轻度慢性GVHD。

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