为肝细胞癌武装 GPC3 CAR-T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Evaluating tumor-infiltrating lymphocytes in hepatocellular carcinoma using hematoxylin and eosin-stained tumor sections.
Evaluating tumor-infiltrating lymphocytes in hepatocellular carcinoma using hematoxylin and eosin-stained tumor sections.
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高浸润淋巴细胞的 HCC 患者往往复发率较低且 MVI 较少。在 H&E 染色标本中评估 TILs 可能成为 HCC 的预后参数。
TIL(肿瘤浸润淋巴细胞)(TILs)是肝细胞癌(HCC)的预后因素。然而,不同的TILs评估方法在分析前、分析中和分析后存在各种挑战。国际免疫肿瘤生物标志物工作组提出的在苏木精和伊红(H&E)染色的肿瘤切片中评估TILs的方法,已被证明在许多肿瘤中是一种可重复、经济且易于应用的方法。
评估TILs在HCC的H&E染色切片中的预后意义。
这是一项在医院进行的回顾性研究。纳入2015年至2017年在中山医院接受肝切除术的HCC患者。排除在此期间术前出现复发或接受抗病毒治疗以外治疗的患者。共204例患者纳入研究。在光学显微镜下以400×放大倍数,对H&E染色的肿瘤切片中的ILs进行人工计数。分别评估肿瘤中心(TILs CT)、浸润前沿(TILs IF)和瘤周(PILs)区域的ILs。使用Cox回归模型进行单因素和多因素生存分析。P < 0.05被认为具有统计学显著性,所有P值均为双侧。
在204例患者中,单因素分析表明,大血管侵犯(MaVI)(P = 0.001)、微血管侵犯(MVI)(P = 0.012)、多发肿瘤(P = 0.008)、大肿瘤(> 10 cm)(P = 0.001)、无肿瘤包膜(P = 0.026)、大梁状组织学亚型(P = 0.001)、TILs CT低密度(P = 0.039)、TILs IF(P = 0.014)和PILs(P = 0.010)是无进展生存期(PFS)的预测因素。Cox多因素分析表明,MaVI(P = 0.009)、无肿瘤包膜(P = 0.031)、TILs IF低密度(P = 0.047)和PILs(P = 0.0495)是PFS的独立预测因素。通过结合TILs CT、TILs IF和PILs进行三分类分析,之后将HCC分为免疫高[(TILs CT)高、(TILs IF)高和PILs高,83例]、免疫中(除免疫高和免疫低亚型以外的肿瘤,94例)和免疫低[(TILs CT)低、(TILs IF)低和PILs低,27例]亚型。免疫高亚型的MVI发生率(40.96%)低于免疫中亚型(61.70%,P = 0.017)和免疫低亚型(66.67%,P = 0.020)。免疫高、免疫中和免疫低亚型的复发率分别为10.8%、25.5%和33.3%。
Tumor-infiltrating lymphocytes (TILs) constitute a prognostic factor in hepatocellular carcinoma (HCC). However, different methods of assessing TILs have various pre-analytical, analytical, and post-analytical challenges. The evaluation of TILs in hematoxylin and eosin (H&E)-stained tumor sections proposed by the International Immuno-Oncology Biomarker Working Group was demonstrated to be a reproducible, affordable and easily applied method in many tumors. AIM: To evaluate the prognostic significance of TILs in H&E-stained slides of HCCs.
This was a retrospective study performed in the hospital. HCC patients who underwent liver resection between 2015 and 2017 in Zhongshan Hospital were enrolled in this study. Patients who experienced recurrence or received therapy in addition to antiviral therapy before surgery at this time were excluded. A total of 204 patients were enrolled in the study. The ILs were counted manually in tumor sections stained with H&E under an optical microscope at 400 ×. The ILs were assessed separately in the center of the tumor (TILs CT ), the invasive front (TILs IF ), and peritumor (PILs) areas. Univariate and multivariate survival analyses were performed using a Cox regression model. P < 0.05 was considered statistically significant and all P -values were two-sided.
Among the 204 patients, univariate analysis indicated that macrovascular invasion (MaVI) ( P = 0.001), microvascular invasion (MVI) ( P = 0.012), multiple tumors ( P = 0.008), large tumors (> 10 cm) ( P = 0.001), absence of a tumor capsule ( P = 0.026), macrotrabecular histological subtype ( P = 0.001), low density of TILs CT ( P = 0.039), TILs IF ( P = 0.014), and PILs ( P = 0.010) were predictors of progression-free survival (PFS). Cox multivariate analysis indicated that MaVI ( P = 0.009), absence of a tumor capsule ( P = 0.031), low-density of TILs IF ( P = 0.047) and PILs ( P = 0.0495) were independent predictors of PFS. A three-category analysis was carried out by combining TILs CT , TILs IF , and PILs, after which HCCs were classified into immune high [(TILs CT ) high , (TILs IF ) high , and PILs high , 83 cases], immune mod (tumors other than immune high and immune low subtypes, 94 cases), and immune low [(TILs CT ) low , (TILs IF ) low , and PILs low , 27 cases)] subtypes. The immune high subtype had a lower rate of MVI (40.96%) than the immune mod (61.70%, P = 0.017) and immune low (66.67%, P = 0.020) subtypes. The recurrence rates of the immune high , immune mod and immune low subtypes were 10.8%, 25.5% and 33.3%, respectively.
HCC patients with high infiltrating lymphocytes tend to have a lower recurrence rate and less MVI. The evaluation of TILs in H&E-stained specimens could be a prognostic parameter for HCC.
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