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疾病进展时间与二线 BTK 抑制剂在复发/难治性套细胞淋巴瘤中的结局

英文原题:Time to progression of disease and outcomes with second-line BTK inhibitors in relapsed/refractory mantle cell lymphoma.

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Time to progression of disease and outcomes with second-line BTK inhibitors in relapsed/refractory mantle cell lymphoma.

PubMed 2023/08/22(内容时间) Blood Adv Q1 · IF 7.7(JCR 2025)

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中文摘要

一线(1L)治疗后疾病进展时间(POD)对套细胞淋巴瘤(MCL)具有预后意义,尽管既往研究涵盖了广泛范围的1L、二线(2L)及后续治疗线数。

本研究的目的是评估仅在接受含利妥昔单抗1L治疗后启动2L Bruton酪氨酸激酶抑制剂(BTKi)的复发/难治性(R/R)MCL患者中预测结局的因素。患者来自8个国际中心(7个主队列,1个验证队列)。构建了评估POD时间与临床/病理因素之间关联的多变量模型,并将其转化为列线图和预后指数以预测该人群的结局。共纳入360例患者,包括主队列160例和验证队列200例。POD时间、Ki67 ≥ 30%和MCL国际预后指数(MIPI)与从2L BTKi开始的无进展生存期(PFS2)和总生存期(OS2)相关。两个队列中C指数均持续≥0.68。构建了基于列线图和预后指数的网页/应用程序计算器以估算PFS2和OS2。2L BTKi MIPI识别出3组具有不同2年PFS2的群体,包括高风险(14%)、中风险(50%)和低风险(64%)。POD时间、Ki67和MIPI与接受2L BTKi的R/R MCL患者的生存结局相关。纳入这些变量的简单临床模型可能有助于规划替代疗法,如CAR-T 细胞疗法、异基因干细胞移植或具有替代作用机制的新药。

展开英文摘要原文

Time to progression of disease (POD) after first-line (1L) therapy is prognostic in mantle cell lymphoma (MCL), although studies have included a broad range of 1L, second-line (2L), and subsequent lines of therapy. The purpose of this study was to evaluate the factors predicting outcomes in patients with relapsed/refractory (R/R) MCL exclusively initiating 2L Bruton's tyrosine kinase inhibitors (BTKis) after 1L rituximab-containing therapy. Patients were accrued from 8 international centers (7 main, 1 validation cohort). Multivariable models evaluating the association between time to POD and clinical/pathologic factors were constructed and converted into nomograms and prognostic indexes predicting outcomes in this population. A total of 360 patients were included, including 160 in the main cohort and 200 in the validation cohort.

Time to POD, Ki67 ≥ 30%, and MCL International Prognostic Index (MIPI) were associated with progression-free survival (PFS2) and overall survival (OS2) from the start of 2L BTKis. C-indexes were consistently ≥0. 68 in both cohorts. Web/application-based calculators based on nomograms and prognostic indexes to estimate PFS2 and OS2 were constructed. The 2L BTKi MIPI identifies 3 groups with distinct 2-year PFS2, including high risk (14%), intermediate risk (50%), and low risk (64%).

Time to POD, Ki67, and MIPI are associated with survival outcomes in patients with R/R MCL receiving 2L BTKis. Simple clinical models incorporating these variables may assist in planning for alternative therapies such as chimeric antigen receptor T-cell therapy, allogeneic stem cell transplantation, or novel agents with alternative mechanisms of action.

论文信息

作者
Villa D、Jiang A、Visco C、Crosbie N、McCulloch R、Buege MJ、Kumar A、Bond DA
第一作者单位
British Columbia Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.Canada
通讯作者单位
Haematology, University Hospitals Plymouth NHS Trust, Plymouth, United Kingdom.United Kingdom
文献类型
美国 NIH 资助研究
期刊
Blood advances2023 Aug 22
原文标识
PubMed 37307169 · DOI 10.1182/bloodadvances.2023009804

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