He Jiaxi, Xu Songhui, Pan Hui, Li Shuben, He Jianxing
Department of Pathology, University of Maryland Baltimore, School of Medicine, Baltimore, MD, USA.
Department of Thoracic Surgery, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Transl Lung Cancer Res. 2020 Aug;9(4):1041-1052. doi: 10.21037/tlcr-19-488.
The 8 edition staging system for malignant pleural mesothelioma (MPM) has been proposed. The size of tumor is not taken into consideration. We intend to elucidate the prognostic value of the size of MPM and evaluate the current staging system via the data of SEER database.
All cases of primary MPM were identified and extracted from the SEER database during the period of 2004-2016. The endpoints were overall survival (OS) and cancer-specific survival (CSS) which were analyzed using Kaplan-Meier method. Log-rank test and Cox regression were utilized to identify the prognostic factors.
A total of 2,138 patients were included in the primary cohort. The 1-, 3- and 5-year survival rates of MPM were 39.4%, 11.8% and 3.8%. Older, male and advanced stage patients accounted for larger proportion of the cohort. Besides tumor extension, lymph node involvement and metastatic status, tumor size, pathological type and differentiation grade were significant prognostic factors. In the stratified analysis of tumor extension, size is a significant prognostic factor in T2 patients and indicates inferior survival outcomes. Surgery, chemotherapy and radiation can increase both OS and CSS in MPM patients. Triple combination treatments showed a superiority to other treatments.
Tumor size matters in the prognosis of MPM especially in the early stage of MPM patients. The adjusted TNM staging system incorporating tumor size has better accuracy than the 8 edition IMIG system. However, some stages had not been fully identified. More cases of early stages are warranted for essential revision.
恶性胸膜间皮瘤(MPM)的第8版分期系统已被提出。肿瘤大小未被纳入考虑。我们打算通过监测、流行病学和最终结果(SEER)数据库的数据阐明MPM大小的预后价值,并评估当前的分期系统。
2004年至2016年期间,从SEER数据库中识别并提取所有原发性MPM病例。终点指标为总生存期(OS)和癌症特异性生存期(CSS),采用Kaplan-Meier法进行分析。利用对数秩检验和Cox回归确定预后因素。
原发性队列共纳入2138例患者。MPM的1年、3年和5年生存率分别为39.4%、11.8%和3.8%。年龄较大、男性和晚期患者在队列中占比更大。除肿瘤侵犯范围、淋巴结受累情况和转移状态外,肿瘤大小、病理类型和分化程度也是重要的预后因素。在肿瘤侵犯范围的分层分析中,大小是T2期患者的重要预后因素,提示生存结局较差。手术、化疗和放疗可提高MPM患者的OS和CSS。三联联合治疗显示出优于其他治疗的效果。
肿瘤大小对MPM的预后很重要,尤其是在MPM患者的早期。纳入肿瘤大小的调整后TNM分期系统比第8版国际间皮瘤研究组(IMIG)系统具有更高的准确性。然而,一些分期尚未得到充分界定。需要更多早期病例进行必要的修订。