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首页> 外文期刊>Oncology letters >Myasthenia gravis in patients with thymoma affects survival rate following extended thymectomy
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Myasthenia gravis in patients with thymoma affects survival rate following extended thymectomy

机译:胸腺瘤患者重症肌无力会影响延长胸腺切除术后的存活率

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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.
机译:胸腺瘤是纵隔前房最常见的成人肿瘤,大量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,用于完全切除可能的异位胸腺以避免复发。关于ET对胸腺瘤患者MG疗效的研究非常有限。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。本研究包括104例行ET的胸腺瘤患者。男性61位(58.7%)和女性43位(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B2型胸腺瘤中最常见。在5年的随访期内,有11名患者死于胸腺瘤复发或MG导致的呼吸衰竭。没有MG或有MG的患者的5年总生存率分别为89.1%和76.0%。 Masaoka I + II和III + IV期患者的总生存率分别为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%。与没有这些特征的患者相比,MG(P = 0.026),Masaoka III + IV期(P = 0.008)和WHO WHO B2 + B3(P = 0.032)患者的预后较差。此外,通过Cox回归进行的多变量分析显示,年龄[P = 0.032;相对风险(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)显着影响OS率。总之,ET是治疗胸腺瘤的可靠方法。 Masaoka早期阶段和无MG的患者均有望长期存活。与没有MG的患者相比,患有MG的胸腺瘤患者的预后较差。本研究结果为胸腺瘤患者的未来治疗提供了有用的信息。

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