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本妥昔单抗维迪昔单抗作为移植患者或 ASCT 失败的初治霍奇金淋巴瘤的挽救治疗:普利亚血液学网络(REP)的真实经验。

Brentuximab vedotin as salvage treatment in Hodgkin lymphoma naïve transplant patients or failing ASCT: the real life experience of Rete Ematologica Pugliese (REP).

机构信息

Department of Hematology and Bone Marrow Transplant, Hospital Card. G. Panico, Via San Pio X, 73039, Tricase, Italy.

Department of Hematology and Bone Marrow Transplant, University of Bari, Policlinico, Bari, Italy.

出版信息

Ann Hematol. 2018 Oct;97(10):1817-1824. doi: 10.1007/s00277-018-3379-5. Epub 2018 Jul 27.

Abstract

Brentuximab vedotin (BV) shows a high overall response rate (ORR) in relapsed/refractory (R/R) Hodgkin lymphoma (HL) after autologous transplant (ASCT). The aim of this multicenter study, conducted in nine Hematology Departments of Rete Ematologica Pugliese, was to retrospectively evaluate the efficacy and safety of BV as salvage therapy and as bridge regimen to ASCT or allogeneic transplant (alloSCT) in R/R HL patients. Seventy patients received BV. Forty-five patients (64%) were treated with BV as bridge to transplant:16 (23%) patients as bridge to ASCT and 29 (41%) as bridge to alloSCT. Twenty-five patients (36%), not eligible for transplant, received BV as salvage treatment. The ORR was 59% (CR 26%). The ORR in transplant naïve patients was 75% (CR 31%). In patients treated with BV as bridge to alloSCT, the ORR was 62% (CR 24%). In a multivariate analysis, the ORR was lower in refractory patients (p < 0.005). The 2y-OS was 70%. The median PFS was 17 months. Ten of the 16 (63%) naïve-transplant patients received ASCT, with 50% in CR before ASCT. In the 29 patients treated with BV as bridge to alloSCT, 28 (97%) proceeded to alloSCT with 25% in CR prior to alloSCT. The most common adverse events were peripheral neuropathy (50%), neutropenia (29%) and anemia (12%). These data suggest that BV is well tolerated and very effective in R/R HL, producing a substantial level of CR. BV may also be a key therapeutic agent to achieve good disease control before transplant, improving post- transplant outcomes, also in refractory and heavily pretreated patients, without significant overlapping toxicities with prior therapies.

摘要

本妥昔单抗维泊妥珠单抗(BV)在自体移植(ASCT)后复发/难治性(R/R)霍奇金淋巴瘤(HL)中显示出高总体缓解率(ORR)。这项多中心研究由普利亚血液学网络(Rete Ematologica Pugliese)的九个血液科进行,旨在回顾性评估 BV 作为挽救治疗以及作为 ASCT 或异基因移植(alloSCT)桥接方案在 R/R HL 患者中的疗效和安全性。70 例患者接受了 BV 治疗。45 例(64%)患者接受 BV 桥接治疗:16 例(23%)患者为 ASCT 桥接,29 例(41%)为 alloSCT 桥接。25 例(36%)不符合移植条件的患者接受 BV 作为挽救治疗。ORR 为 59%(完全缓解率[CR]26%)。移植初治患者的 ORR 为 75%(CR 31%)。接受 alloSCT 桥接治疗的患者的 ORR 为 62%(CR 24%)。在多变量分析中,难治性患者的 ORR 较低(p<0.005)。2 年总生存率(OS)为 70%。中位无进展生存期(PFS)为 17 个月。16 例初治移植患者中有 10 例(63%)接受了 ASCT,其中 50%在 ASCT 前达到 CR。29 例接受 alloSCT 桥接治疗的患者中,28 例(97%)进行了 alloSCT,其中 25%在 alloSCT 前达到 CR。最常见的不良反应是周围神经病(50%)、中性粒细胞减少症(29%)和贫血(12%)。这些数据表明,BV 在 R/R HL 中耐受性良好且非常有效,产生了相当水平的 CR。BV 也可能是一种关键的治疗药物,可在移植前实现良好的疾病控制,提高移植后的结果,即使在难治性和预处理较多的患者中也是如此,且与先前的治疗方案没有明显的毒性重叠。

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