Department of Internal Medicine, University of Florida, Gainesville, Florida, USA.
College of Medicine, University of Florida, Gainesville, Florida, USA.
Cancer Rep (Hoboken). 2023 Mar;6(3):e1750. doi: 10.1002/cnr2.1750. Epub 2022 Nov 12.
Thymic epithelial tumors are rare and include thymomas and thymic carcinomas. There is scarce literature characterizing prognostic factors and long-term outcomes in these tumors.
This review aims to describe disease features of thymomas and thymic carcinomas and to report clinical differences among thymoma histological subtypes.
A retrospective chart review was performed at the University of Florida Shands Hospital, a tertiary care academic medical center in Gainesville, Florida, USA. The review included clinical data of adults with thymic epithelial tumors diagnosed between 2001 and 2021. Significant associations among demographics, histology, stage, and outcomes were investigated. Thymoma subgroup analysis was performed using histological subtype and sex. Forty patients with thymoma and seven patients with thymic carcinoma were included in the final analysis. Among those with thymomas, patients with subtype B1, B2, or B3 tumors were younger, had larger tumors, and presented with higher stage disease when compared to those with subtypes A or AB. Tumor recurrence was most common in subtype B2 and B3 tumors (50.0% and 16.7% vs. 0%; p < .01). However, there was no significant difference in overall survival between histologic subtypes. Compared to females, males with thymomas had superior overall survival (103.0 vs. 62.9 months; p = .021) despite presenting with larger tumors (9.8 vs. 5.8 cm; p = .041). Concomitant myasthenia gravis was associated with increased recurrence but not worsened mortality. Compared to thymomas, patients with thymic carcinoma presented with higher-stage disease and had poorer 5-year survival (50.0% vs. 93.1%; p < .01).
This study affirmed pathologic stage and resectability as prognostic factors for thymic epithelial tumors. New findings include inferior overall survival in female patients and higher recurrence rates in those with thymomas and concomitant myasthenia gravis.
胸腺上皮肿瘤较为罕见,包括胸腺瘤和胸腺癌。关于这些肿瘤的预后因素和长期结果,文献记载较少。
本综述旨在描述胸腺瘤和胸腺癌的疾病特征,并报告胸腺瘤组织学亚型之间的临床差异。
在美国佛罗里达州盖恩斯维尔市的佛罗里达大学 Shands 医院进行了一项回顾性病历审查,该医院是一家三级保健学术医疗中心。该审查纳入了 2001 年至 2021 年间诊断为胸腺上皮肿瘤的成年患者的临床数据。研究了人口统计学、组织学、分期和结果之间的显著关联。使用组织学亚型和性别对胸腺瘤亚组进行分析。最终分析纳入了 40 例胸腺瘤患者和 7 例胸腺癌患者。在胸腺瘤患者中,B1、B2 或 B3 型肿瘤患者更年轻,肿瘤更大,且分期更高。B2 和 B3 型肿瘤的肿瘤复发最为常见(50.0%和 16.7% vs. 0%;p < .01)。然而,组织学亚型之间的总生存率没有显著差异。与女性相比,胸腺瘤男性的总生存率更高(103.0 与 62.9 个月;p = .021),尽管肿瘤更大(9.8 与 5.8 厘米;p = .041)。同时合并重症肌无力与复发增加相关,但与死亡率恶化无关。与胸腺瘤相比,胸腺癌患者分期更高,5 年生存率更差(50.0% 与 93.1%;p < .01)。
本研究证实了病理分期和可切除性是胸腺上皮肿瘤的预后因素。新发现包括女性患者的总体生存率降低,以及同时合并重症肌无力的胸腺瘤患者的复发率更高。