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硼替佐米联合利妥昔单抗、高剂量阿糖胞苷和地塞米松治疗复发或难治性套细胞淋巴瘤:欧洲套细胞淋巴瘤网络的一项随机、开放标签 III 期试验。

The addition of bortezomib to rituximab, high-dose cytarabine and dexamethasone in relapsed or refractory mantle cell lymphoma-a randomized, open-label phase III trial of the European mantle cell lymphoma network.

机构信息

Department of Medicine III, LMU University Hospital, LMU Munich, Munich, Germany.

Institute for Medical Information Processing, Biometry and Epidemiology, LMU Munich, Munich, Germany.

出版信息

Leukemia. 2024 Jun;38(6):1307-1314. doi: 10.1038/s41375-024-02254-2. Epub 2024 Apr 27.

Abstract

The therapy of relapsed or refractory (r/r) mantle cell lymphoma (MCL) patients remains a major clinical challenge to date. We conducted a randomized, open-label, parallel-group phase-III trial hypothesizing superior efficacy of rituximab, high-dose cytarabine and dexamethasone with bortezomib (R-HAD + B) versus without (R-HAD) in r/r MCL ineligible for or relapsed after autologous stem cell transplant (ASCT). Primary endpoint was time to treatment failure (TTF), secondary endpoints included response rates, progression free survival, overall survival, and safety. In total, 128 of 175 planned patients were randomized to R-HAD + B (n = 64) or R-HAD (n = 64). Median TTF was 12 vs. 2.6 months (p = 0.045, MIPI-adjusted HR 0.69; 95%CI 0.47-1.02). Overall and complete response rates were 63 vs. 45% (p = 0.049) and 42 vs. 19% (p = 0.0062). A significant treatment effect was seen in the subgroup of patients >65 years (aHR 0.48, 0.29-0.79) and without previous ASCT (aHR 0.52, 0.28-0.96). Toxicity was mostly hematological and attributable to the chemotherapeutic backbone. Grade ≥3 leukocytopenia and lymphocytopenia were more common in R-HAD + B without differences in severe infections between both arms. Bortezomib in combination with chemotherapy can be effective in r/r MCL and should be evaluated further as a therapeutic option, especially if therapy with BTK inhibitors is not an option. Trial registration: NCT01449344.

摘要

复发或难治性(r/r)套细胞淋巴瘤(MCL)患者的治疗仍然是一个重大的临床挑战。我们进行了一项随机、开放标签、平行组 III 期试验,假设利妥昔单抗、高剂量阿糖胞苷和地塞米松联合硼替佐米(R-HAD+B)与不联合(R-HAD)在不适合或自体干细胞移植(ASCT)后复发的 r/r MCL 患者中的疗效更优。主要终点是治疗失败时间(TTF),次要终点包括缓解率、无进展生存期、总生存期和安全性。总共,175 名计划患者中有 128 名被随机分配到 R-HAD+B(n=64)或 R-HAD(n=64)。中位 TTF 为 12 个月 vs. 2.6 个月(p=0.045,MIPI 调整 HR 0.69;95%CI 0.47-1.02)。总缓解率和完全缓解率分别为 63% vs. 45%(p=0.049)和 42% vs. 19%(p=0.0062)。在年龄>65 岁(aHR 0.48,0.29-0.79)和无先前 ASCT(aHR 0.52,0.28-0.96)的患者亚组中观察到显著的治疗效果。毒性主要是血液学毒性,与化疗基础有关。R-HAD+B 中更常见 3 级及以上白细胞减少症和淋巴细胞减少症,但两组严重感染发生率无差异。硼替佐米联合化疗对 r/r MCL 有效,应作为一种治疗选择进一步评估,尤其是在不能使用 BTK 抑制剂治疗的情况下。试验注册:NCT01449344。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3440/11147755/d8011625eff1/41375_2024_2254_Fig1_HTML.jpg

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