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胸腺瘤患者的重症肌无力会影响扩大胸腺切除术后的生存率。

Myasthenia gravis in patients with thymoma affects survival rate following extended thymectomy.

作者信息

Zhang Zhefeng, Cui Youbin, Jia Rui, Xue Lei, Liang Huagang

机构信息

Department of Thoracic Surgery, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei 066000, P.R. China.

Department of Thoracic Surgery, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.

出版信息

Oncol Lett. 2016 Jun;11(6):4177-4182. doi: 10.3892/ol.2016.4528. Epub 2016 May 5.

Abstract

Thymomas are the most common adult tumors in the anterior mediastinal compartment, and a significant amount of thymomas are complicated by myasthenia gravis (MG). Extended thymectomy (ET) is the primary treatment method for thymomas and is used to completely resect possible ectopic thymus to avoid recurrence. Studies on the effect of MG in thymoma patients following ET are limited. The aim of the present study was to determine whether the presence of MG affects the prognosis of patients with thymoma. The present study consisted of 104 patients with thymoma that underwent ET; 61 men (58.7%) and 43 women (41.3%) (mean age, 54.6 years). In total, 38 patients had MG (36.5%). MG was most frequently observed in World Health Organization (WHO) classification type B2 thymoma compared with other types of thymoma. During the 5-year follow-up period, 11 patients succumbed to a recurrence of thymoma or respiratory failure due to MG. The overall 5-year survival rate in patients without MG or with MG was 89.1 and 76.0%, respectively. The overall survival (OS) rate in patients with Masaoka stages I + II and III + IV was 90.0 and 68.0%, respectively. The OS rate in patients with WHO type A + AB + B1 and type B2 + B3 was 96.9 and 76.8%, respectively. The patients with MG (P=0.026), Masaoka stages III + IV (P=0.008) and WHO type B2 + B3 (P=0.032) had a poorer prognosis compared with patients without these characteristics. Furthermore, multivariate analysis by Cox regression revealed that age [P=0.032; relative risk (RR)=1.097; 95% confidence interval (CI)=1.097-1.192] and MG (P=0.042; RR=0.167; 95% CI=0.037-0.940) significantly affected OS rate. In summary, ET is a reliable method for the treatment of thymoma. Long-term survival is expected for patients at early Masaoka stages, and for patients without MG. The prognosis of patients with thymomas with MG is poorer compared with patients without MG. The present findings provide useful information for the future management of patients with thymomas.

摘要

胸腺瘤是前纵隔最常见的成人肿瘤,相当数量的胸腺瘤合并重症肌无力(MG)。扩大胸腺切除术(ET)是胸腺瘤的主要治疗方法,用于完全切除可能存在的异位胸腺以避免复发。关于ET后MG对胸腺瘤患者影响的研究有限。本研究的目的是确定MG的存在是否会影响胸腺瘤患者的预后。本研究纳入了104例行ET的胸腺瘤患者;其中男性61例(58.7%),女性43例(41.3%)(平均年龄54.6岁)。共有38例患者患有MG(36.5%)。与其他类型的胸腺瘤相比,MG在世界卫生组织(WHO)分类的B2型胸腺瘤中最为常见。在5年的随访期内,11例患者因胸腺瘤复发或MG导致呼吸衰竭死亡。无MG或有MG患者的5年总生存率分别为89.1%和76.0%。Masaoka分期I + II期和III + IV期患者的总生存(OS)率分别为90.0%和68.0%。WHO A + AB + B1型和B2 + B3型患者的OS率分别为96.9%和76.8%。与无这些特征的患者相比,患有MG(P = 0.026)、Masaoka分期III + IV期(P = 0.008)和WHO B2 + B3型(P = 0.032)的患者预后较差。此外,Cox回归多因素分析显示年龄[P = 0.032;相对危险度(RR)= 1.097;95%置信区间(CI)= 1.097 - 1.192]和MG(P = 0.042;RR = 0.167;95% CI = 0.037 - 0.940)显著影响OS率。总之,ET是治疗胸腺瘤的可靠方法。Masaoka早期阶段且无MG的患者有望获得长期生存。与无MG的胸腺瘤患者相比,有MG的患者预后较差。本研究结果为胸腺瘤患者的未来管理提供了有用信息。

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