Ruffini Enrico, Detterbeck Frank, Van Raemdonck Dirk, Rocco Gaetano, Thomas Pascal, Weder Walter, Brunelli Alessandro, Evangelista Andrea, Venuta Federico
Department of Surgery, Section of Thoracic Surgery, University of Torino, Torino, Italy
Department of Surgery, Section of Thoracic Surgery, Yale University, New Haven, CT, USA.
Eur J Cardiothorac Surg. 2014 Sep;46(3):361-8. doi: 10.1093/ejcts/ezt649. Epub 2014 Jan 30.
A retrospective database was developed by the European Society of Thoracic Surgeons, collecting patients submitted to surgery for thymic tumours to analyse clinico-pathological prognostic predictors.
A total of 2151 incident cases from 35 institutions were collected from 1990 to 2010. Clinical-pathological characteristics were analysed, including age, gender, associated myasthenia gravis stage (Masaoka), World Health Organization histology, type of thymic tumour [thymoma, thymic carcinoma (TC), neuroendocrine thymic tumour (NETT)], type of resection (complete/incomplete), tumour size, adjuvant therapy and recurrence. Primary outcome was overall survival (OS); secondary outcomes were the proportion of incomplete resections, disease-free survival and the cumulative incidence of recurrence (CIR).
A total of 2030 patients were analysed for OS (1798 thymomas, 191 TCs and 41 NETTs). Ten-year OS was 0.73 (95% confidence interval 0.69-0.75). Complete resection (R0) was achieved in 88% of the patients. Ten-year CIR was 0.12 (0.10-0.15). Predictors of shorter OS were increased age (P < 0-001), stage [III vs I HR 2.66, 1.80-3.92; IV vs I hazard ratio (HR) 4.41, 2.67-7.26], TC (HR 2.39, 1.68-3.40) and NETT (HR 2.59, 1.35-4.99) vs thymomas and incomplete resection (HR 1.74, 1.18-2.57). Risk of recurrence increased with tumour size (P = 0.003), stage (III vs I HR 5.67, 2.80-11.45; IV vs I HR 13.08, 5.70-30.03) and NETT (HR 7.18, 3.48-14.82). Analysis using a propensity score indicates that the administration of adjuvant therapy was beneficial in increasing OS (HR 0.69, 0.49-0.97) in R0 resections.
Masaoka stages III-IV, incomplete resection and non-thymoma histology showed a significant impact in increasing recurrence and in worsening survival. The administration of adjuvant therapy after complete resection is associated with improved survival.
欧洲胸外科医师协会建立了一个回顾性数据库,收集接受胸腺肿瘤手术的患者资料,以分析临床病理预后预测因素。
1990年至2010年共收集了来自35个机构的2151例新发病例。分析临床病理特征,包括年龄、性别、相关重症肌无力分期(马萨oka)、世界卫生组织组织学类型、胸腺肿瘤类型[胸腺瘤、胸腺癌(TC)、神经内分泌胸腺肿瘤(NETT)]、切除类型(完全/不完全)、肿瘤大小、辅助治疗和复发情况。主要结局是总生存期(OS);次要结局是不完全切除的比例、无病生存期和复发累积发生率(CIR)。
共对2030例患者进行了OS分析(1798例胸腺瘤、191例TC和41例NETT)。10年OS为0.73(95%置信区间0.69 - 0.75)。88%的患者实现了完全切除(R0)。10年CIR为0.12(0.10 - 0.15)。OS较短的预测因素包括年龄增加(P < 0.001)、分期[III期与I期HR 2.66,1.80 - 3.92;IV期与I期风险比(HR)4.41,2.67 - 7.26]、TC(HR 2.39,1.68 - 3.40)和NETT(HR 2.59,1.35 - 4.99)与胸腺瘤相比以及不完全切除(HR 1.74,1.18 - 2.57)。复发风险随肿瘤大小增加(P = 0.003)、分期增加(III期与I期HR 5.67,2.80 - 11.45;IV期与I期HR 13.08,5.70 - 30.0)和NETT(HR 7.18,3.48 - 14.82)而增加。使用倾向评分分析表明,辅助治疗在R0切除中对提高OS有益(HR 0.69,0.49 - 0.97)。
马萨oka III - IV期、不完全切除和非胸腺瘤组织学对增加复发和恶化生存有显著影响。完全切除后给予辅助治疗与生存率提高相关。