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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Prognostic model for relapsed/refractory transplant-ineligible diffuse large B-cell lymphoma utilizing the lymphocyte-to-monocyte ratio.
Prognostic model for relapsed/refractory transplant-ineligible diffuse large B-cell lymphoma utilizing the lymphocyte-to-monocyte ratio.
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我们开展了一项多机构回顾性研究,纳入100例不适合移植(TI)的弥漫性大B细胞淋巴瘤(DLBCL)患者,这些患者在一线R-CHOP(或类似方案)治疗后复发或进展,旨在为TI复发/难治性(r/r)DLBCL建立稳健的预测模型,因为除CAR-T 细胞治疗或双特异性抗体外,目前可用治疗方式下该病预后异质性大且较差。复发或进展时的中位年龄为76岁。自首次进展起的中位无进展生存期(PFS)和总生存期(OS)分别为11.5个月和21.9个月。多因素分析确定,进展时低淋巴细胞与单核细胞比值(LMR)、高乳酸脱氢酶升高和高C反应蛋白升高是OS的独立预测因素。基于这三个因素的预测模型,此处命名为r/r DLBCL京都预后指数(KPI-R),成功以统计学显著性对其OS和PFS进行了分层。
此外,R-CHOP的无事件生存期少于24个月和低LMR被确定为任何序列挽救治疗无应答的重要预测因素。我们得出结论,LMR是TI r/r DLBCL患者治疗反应和预后的真正预测因素,可能有助于治疗决策。
We conducted a multi-institutional retrospective study in 100 transplant-ineligible (TI) patients with diffuse large B-cell lymphoma (DLBCL) that relapsed or progressed after first-line R-CHOP (or -like) therapy to develop a robust predictive model for TI relapsed/refractory (r/r) DLBCL, which has a heterogeneous but poor prognosis by currently available treatment modalities other than chimeric antigen receptor T-cell (CAR-T) therapy or bispecific antibodies. The median age at relapse or progression was 76 years.
The median progression-free survival (PFS) and overall survival (OS) from the first progression were 11. 5 months and 21. 9 months, respectively. Multivariate analysis identified low lymphocyte-to-monocyte ratio (LMR), elevated high lactate dehydrogenase, and elevated C-reactive protein at progression as independent predictors of OS. A predictive model based on these three factors, here designated as the Kyoto Prognostic Index for r/r DLBCL (KPI-R), successfully stratified their OS and PFS with statistical significance.
In addition, event-free survival less than 24 months for R-CHOP and low LMR were identified as significant predictive factors for non-response in any sequence of salvage therapy.
We concluded that LMR is a bonafide predictor of treatment response and prognosis in patients with TI r/r DLBCL, and may be helpful in treatment decision-making.
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