Frasca Luca, Sarubbi Antonio, Longo Filippo, Marziali Valentina, Patirelis Alexandro, Crucitti Pierfilippo, Ambrogi Vincenzo
Department of Thoracic Surgery, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro Del Portillo 200, 00128, Rome, Italy.
Doctoral School of Microbiology, Immunology, Infectious Diseases and Transplants (MIMIT), Tor Vergata University, Viale Oxford 81, 00133, Rome, Italy.
Updates Surg. 2025 May 25. doi: 10.1007/s13304-025-02242-w.
Thymomas are one of the most common neoplasms of the anterior mediastinum with limited therapeutic options, particularly in advanced stages. The molecular profiles of these tumors remain poorly investigated. This study aims to evaluate the expression of programmed death ligand 1 (PD-L1) in a selected cohort of intentionally curative resected thymomas and evaluate a possible relationship with the risk of recurrence. This retrospective bicentric study analyzed a group of patients who underwent complete thymectomy with curative intent. PD-L1 expression was assessed through immunohistochemistry using the Ventana PD-L1 assay. PD-L1 expression was assessed as low if <50% or high when ≥50%. The Kaplan-Meier method and Cox regression analysis were performed to evaluate a possible relationship between PD-L1 expression and disease-free survival. High PD-L1 expression was observed in 46.2% of patients. Overexpression of this protein was significantly associated with aggressive (B2/B3) thymomas histotypes (p<0.001). During follow-up period, 12/52 patients developed recurrence. High PD-L1 expression correlated with reduced disease-free survival with Kaplan-Meier method (p<0.001). Furthermore, PD-L1 expression more than 50% resulted to be related to a worse prognosis at multivariable Cox regression analysis (hazard ratio 5.4, 95% confidence interval 1.5-16.9, p=0.028) together with histology (p=0.044) and Masaoka-Koga stage (p=0.026). The elevated expression of PD-L1, particularly in aggressive thymoma subtypes, underscores its potential as a prognostic biomarker. These findings support the need for further research to explore the potential of immunotherapy in treating these rare malignancies.
胸腺瘤是前纵隔最常见的肿瘤之一,治疗选择有限,尤其是在晚期。这些肿瘤的分子特征仍未得到充分研究。本研究旨在评估一组经根治性切除的胸腺瘤中程序性死亡配体1(PD-L1)的表达情况,并评估其与复发风险之间的可能关系。这项回顾性双中心研究分析了一组接受根治性胸腺切除术的患者。通过免疫组织化学使用Ventana PD-L1检测法评估PD-L1表达。如果<50%,则PD-L1表达被评估为低表达;如果≥50%,则为高表达。采用Kaplan-Meier法和Cox回归分析来评估PD-L1表达与无病生存期之间的可能关系。46.2%的患者观察到高PD-L1表达。该蛋白的过表达与侵袭性(B2/B3)胸腺瘤组织学类型显著相关(p<0.001)。在随访期间,12/52例患者出现复发。采用Kaplan-Meier法,高PD-L1表达与无病生存期缩短相关(p<0.001)。此外,在多变量Cox回归分析中,PD-L1表达超过50%与预后较差相关(风险比5.4,95%置信区间1.5-16.9,p=0.028),同时与组织学(p=0.044)和Masaoka-Koga分期(p=0.026)有关。PD-L1的高表达,特别是在侵袭性胸腺瘤亚型中,突出了其作为预后生物标志物的潜力。这些发现支持进一步研究以探索免疫疗法治疗这些罕见恶性肿瘤的潜力的必要性。