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在异基因干细胞移植后复发的经典型霍奇金淋巴瘤患者中靶向PD-1通路是安全有效的。

Targeting the PD-1 pathway in patients with relapsed classic Hodgkin lymphoma following allogeneic stem cell transplant is safe and effective.

作者信息

Villasboas Jose Caetano, Ansell Stephen M, Witzig Thomas E

机构信息

Mayo Clinic, Rochester, MN, USA.

出版信息

Oncotarget. 2016 Mar 15;7(11):13260-13264. doi: 10.18632/oncotarget.7177.

Abstract

Patients with classic Hodgkin lymphoma (cHL) that has relapsed after autologous or allogeneic transplant have limited treatment options and a poor prognosis. Immunotherapy with agents that target the PROGRAMMED DEATH 1 (PD-1) receptor have demonstrated clinical activity with durable responses in early-phase clinical trials in this patient population; however, patients with a history of allogeneic stem cell transplantation (SCT) were intentionally excluded from participation in those studies due to concerns for reactivation of graft-versus-host disease (GVHD). We describe the clinical course of two patients with advanced cHL and prior treatment with allogeneic stem cell transplantation (SCT) that were treated with the PD-1 inhibitor pembrolizumab. Both patients had no active graft-versus-host disease (GVHD) at the time initiation of therapy and were maintained on low-dose prednisone. Treatment with pembrolizumab was well tolerated and not associated with reactivation of GVHD. Both patients responded (1 partial, 1 complete) and remain on therapy as of November 30, 2015. This report indicates that immunotherapy targeting the PD-1 pathway can be safely administered to patients with cHL and a history of allogeneic SCT and produce tumor responses. Further studies in this patient population are needed.

摘要

经典型霍奇金淋巴瘤(cHL)患者在自体或异基因移植后复发,治疗选择有限且预后较差。在该患者群体的早期临床试验中,使用靶向程序性死亡1(PD-1)受体的药物进行免疫治疗已显示出临床活性和持久反应;然而,由于担心移植物抗宿主病(GVHD)复发,有过异基因干细胞移植(SCT)病史的患者被有意排除在这些研究之外。我们描述了两名晚期cHL患者和既往接受过异基因干细胞移植(SCT)并接受PD-1抑制剂帕博利珠单抗治疗的患者的临床病程。两名患者在开始治疗时均无活动性移植物抗宿主病(GVHD),并维持使用低剂量泼尼松。帕博利珠单抗治疗耐受性良好,且与GVHD复发无关。两名患者均有反应(1例部分缓解,1例完全缓解),截至2015年11月30日仍在接受治疗。本报告表明,针对PD-1途径的免疫治疗可安全用于有cHL病史和异基因SCT病史的患者,并产生肿瘤反应。需要对该患者群体进行进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c964/4914357/23eb1376bfb8/oncotarget-07-13260-g001.jpg

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