CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Time to progression of disease and outcomes with second-line BTK inhibitors in relapsed/refractory mantle cell lymphoma.
Time to progression of disease and outcomes with second-line BTK inhibitors in relapsed/refractory mantle cell lymphoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
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。
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.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
READING GUIDES
了解这条资料涉及的技术、疾病或试验登记信息,再回到原始来源核实。
MEMBER ACCOUNT
登录成功会直接打开下一页。