Matching-adjusted indirect comparisons of zanubrutinib (MAGNOLIA, BGB-3111-AU-003) versus ibrutinib (PCYC-1121) and rituximab (CHRONOS-3) in relapsed/refractory marginal zone lymphoma.

IF 2.2 4区 医学 Q3 HEMATOLOGY
Catherine Thieblemont, Björn E Wahlin, Leyla Mohseninejad, Kaijun Wang, Ina Zhang, Sam Keeping, Keri Yang, Pier L Zinzani
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引用次数: 0

Abstract

In the absence of head-to-head randomized trials, unanchored matching-adjusted indirect comparisons were conducted to estimate the relative efficacy of zanubrutinib versus ibrutinib and zanubrutinib versus rituximab in relapsed or refractory marginal zone lymphoma (MZL). Logistic propensity score models were used to estimate weights for the patient-level data from two phase II single-arm trials, MAGNOLIA and BGB-3111-AU-003, such that their characteristics matched the ibrutinib and rituximab aggregate-level data from PCYC-1121 and CHRONOS-3, respectively. The base case model for each comparison incorporated four key prognostic factors: prior lines of therapy, MZL subtype, response to prior therapy, and age. A sensitivity analysis incorporating additional prognostic factors was also conducted for the ibrutinib comparison. The impact of each covariate was explored via a leave-one-out analysis. Compared with ibrutinib and rituximab, zanubrutinib demonstrated significant benefits in terms of both overall response and progression-free survival in patients with previously treated MZL.

在复发/难治性边缘区淋巴瘤中,扎鲁替尼 (MAGNOLIA, BGB-3111-AU-003) 与伊布替尼 (PCYC-1121) 和利妥昔单抗 (CHRONOS-3) 的匹配调整间接比较。
在没有头对头随机试验的情况下,我们进行了非锚定匹配调整间接比较,以估算复发或难治性边缘区淋巴瘤(MZL)中扎鲁替尼与伊布替尼、扎鲁替尼与利妥昔单抗的相对疗效。我们使用逻辑倾向评分模型来估算来自两项II期单臂试验(MAGNOLIA和BGB-3111-AU-003)的患者水平数据的权重,使其特征分别与来自PCYC-1121和CHRONOS-3的伊布替尼和利妥昔单抗总体水平数据相匹配。每项比较的基础病例模型都纳入了四个关键预后因素:既往治疗方案、MZL 亚型、对既往治疗的反应和年龄。针对伊布替尼对比还进行了纳入其他预后因素的敏感性分析。每个协变量的影响均通过撇除分析进行了探讨。与伊布替尼和利妥昔单抗相比,扎鲁替尼在既往接受过治疗的MZL患者的总体反应和无进展生存期方面均有显著优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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