Department of Pathology, Hopital des forces de sécurité intérieure de la Marsa, Tunis, Tunisia.
Faculty of Medecine of Tunis, Tunis Manar University, Tunis, Tunisia.
J Egypt Natl Canc Inst. 2024 Mar 25;36(1):9. doi: 10.1186/s43046-024-00212-8.
Tumor-infiltrating lymphocytes (TILs) and the derived immunoscore (IS) have gained considerable attention over the last decade as prognostic markers in many solid cancers. However, in bladder cancer (BC), their prognostic value is not clearly established.
The present study aimed to quantify the TILs rates in BC, assess the derived immunoscore, and investigate their prognostic value. An immunochemistry-based quantification of the different subtypes of TILS was performed on paraffin-embedded blocks from patients with invasive urothelial carcinoma of the bladder. We have assessed the rates of TILs, respectively, on peri-tumoral (PT) and intra-tumoral (IT) areas and calculated for each case the corresponding IS which is the index: CD8+/CD3+ TILs. The IS was then classified as low (I0, I1) or high (I2, I3, I4). We included 30 cases in the analysis.
The median age of patients was 65 years with a sex ratio of 9. TILs densities and distribution were significantly variable between IT and PT areas CD3+ (p = 0.03) and CD8+ (p = 0.004) with the highest rates on the PT areas. In univariate analysis, a low density of CD8+ TILs was significantly associated with an advanced age (p = 0.05), with the presence of lympho-vascular invasion (p = 0.02) and with the absence of specific histological subtype (p = 0.05). A low immunoscore was significantly associated with the presence of lympho-vascular invasion (p = 0.004). No significant association was found between TILs subpopulations, the IS, and the other clinicopathological and survival data. The overall survival (OS) and disease-free survival (DFS) medians were slightly superior in highly T (CD3+/CD8+)-cell infiltrated tumors as well as tumors with a high IS densities. However, the univariate analysis showed that TILs and immunoscore did not impact overall survival (OS) and disease-free survival (DFS).
TILs and immunoscore might be effective prognostic tools in BC. However, standardized quantification methods and further investigation on larger samples are highly recommended to definitively attest the prognostic value of TILs and IS in BC.
在过去十年中,肿瘤浸润淋巴细胞(TILs)及其衍生的免疫评分(IS)作为许多实体瘤的预后标志物受到了广泛关注。然而,在膀胱癌(BC)中,其预后价值尚不清楚。
本研究旨在定量评估 BC 中的 TILs 率,评估衍生的免疫评分,并研究其预后价值。对石蜡包埋的浸润性尿路上皮膀胱癌患者的组织块进行基于免疫化学的不同 TILS 亚型的定量评估。我们分别评估了肿瘤周围(PT)和肿瘤内(IT)区域的 TILs 率,并为每个病例计算了相应的 IS,即指数:CD8+/CD3+ TILs。然后将 IS 分为低(I0、I1)或高(I2、I3、I4)。我们对 30 例病例进行了分析。
患者的中位年龄为 65 岁,性别比为 9。IT 和 PT 区域的 CD3+(p = 0.03)和 CD8+(p = 0.004)的 TILs 密度和分布存在显著差异,PT 区域的 TILs 密度和分布最高。在单因素分析中,低密度的 CD8+TILs 与高龄(p = 0.05)、淋巴血管侵犯(p = 0.02)和缺乏特定组织学亚型(p = 0.05)显著相关。低免疫评分与淋巴血管侵犯显著相关(p = 0.004)。TILs 亚群、IS 与其他临床病理和生存数据之间无显著相关性。高 T(CD3+/CD8+)细胞浸润肿瘤和高 IS 密度肿瘤的总生存期(OS)和无病生存期(DFS)中位数稍高。然而,单因素分析表明 TILs 和免疫评分对总生存期(OS)和无病生存期(DFS)没有影响。
TILs 和免疫评分可能是 BC 的有效预后工具。然而,强烈建议采用标准化的定量方法并对更大的样本进行进一步研究,以明确证明 TILs 和 IS 在 BC 中的预后价值。