不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Tumor-infiltrating T lymphocytes evaluated using digital image analysis predict the prognosis of patients with diffuse large B-cell lymphoma.
Tumor-infiltrating T lymphocytes evaluated using digital image analysis predict the prognosis of patients with diffuse large B-cell lymphoma.
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DLBCL 患者中 TIL-T-Max 高者的预后显著优于 TIL-T-Max 低者,且 TIL-T-Max 是总生存期的独立指标。这些结果表明,使用数字病理系统评估 TIL-T 比值有助于预测 DLBCL 患者的预后。
弥漫大B细胞淋巴瘤(DLBCL)中肿瘤浸润性T淋巴细胞(TIL-T)存在的意义尚待阐明。我们旨在研究TIL-T水平对DLBCL患者预后的影响。
研究共纳入96例DLBCL患者。使用数字病理软件包QuPath测量TIL-T比值。对每例患者的三个焦点(最高、中等和最低)进行TIL-T比值研究,分别得出TIL-T-Max、TIL-T-Intermediate和TIL-T-Min。探讨了TIL-T比值与预后之间的关系。
当以19%作为TIL-T-Max的截断值时,72例(75.0%)和24例(25.0%)患者分别为高TIL-T-Max和低TIL-T-Max。高TIL-T-Max与较低的血清乳酸脱氢酶水平(p < .001)、RCHOP治疗后达到完全缓解的患者组(p < .001)以及低危修订版国际预后指数评分(p < .001)显著相关。单因素分析显示,与高TIL-T-Max患者相比,低TIL-T-Max患者在总生存期方面预后显著更差(p < .001);在Cox比例风险多因素分析中,这一差异仍然显著(风险比,7.55;95%置信区间,2.54至22.42;p < .001)。
The implication of the presence of tumor-infiltrating T lymphocytes (TIL-T) in diffuse large B-cell lymphoma (DLBCL) is yet to be elucidated. We aimed to investigate the effect of TIL-T levels on the prognosis of patients with DLBCL.
Ninety-six patients with DLBCL were enrolled in the study. The TIL-T ratio was measured using QuPath, a digital pathology software package. The TIL-T ratio was investigated in three foci (highest, intermediate, and lowest) for each case, resulting in TIL-T-Max, TIL-T-Intermediate, and TIL-T-Min. The relationship between the TIL-T ratios and prognosis was investigated.
When 19% was used as the cutoff value for TIL-T-Max, 72 (75.0%) and 24 (25.0%) patients had high and low TIL-T-Max, respectively. A high TIL-T-Max was significantly associated with lower serum lactate dehydrogenase levels (p < .001), with patient group who achieved complete remission after RCHOP therapy (p < .001), and a low-risk revised International Prognostic Index score (p < .001). Univariate analysis showed that patients with a low TIL-T-Max had a significantly worse prognosis in overall survival compared to those with a high TIL-T-Max (p < .001); this difference remained significant in a multivariate analysis with Cox proportional hazards (hazard ratio, 7.55; 95% confidence interval, 2.54 to 22.42; p < .001).
Patients with DLBCL with a high TIL-T-Max showed significantly better prognosis than those with a low TIL-T-Max, and the TIL-T-Max was an independent indicator of overall survival. These results suggest that evaluating TIL-T ratios using a digital pathology system is useful in predicting the prognosis of patients with DLBCL.
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