Clinical and histological analysis of malignant mesothelioma - a comprehensive state-wide study

Nicola Pferdmenges, V. Krieg, A. Schulze, H. Kajueter, G. Evers, M. Mohr, L. Schmidt, H. Hense, O. Heidinger, R. Wiewrodt
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Abstract

Background: The cancer registry Northrhine-Westphalia (CR NRW) is state-law based, prospective cancer registry, including all state residents with the diagnosis of cancer (NRW counts approx. 18 million residents). Methods: All MM cases diagnosed and collected between 2010 and 2012 in CR NRW were included (n=1199). 232 cases contained incomplete datasets. In 755 of 967 valid cases (78.1%) the original pathology report was visible, in 468 cases (48.4%) including immunohistochemistry. Results: Of 967 patients with MM 796 were male (82.3%) and 171 female (17.7%), 81.8% were already diseased upon last validation date. Based on ICD-codes 885 patients (91.5%) suffered from pleural MM (C45.0), 72 (7.4%) had peritoneal MM, 2 (0.2%) pericardial MM and 8 (0.8%) had various MM locations. Histology showed predominantly epithelioid growing pattern (60.4%), followed by biphasic growth (13.4%) and sarcomatoid growth (9.4%); in 16.8% the growing pattern was not defined. Median overall survival (OS) of pleural MM was 12.4 months (95%KI 11.3-13.4; all histologies), OS of peritoneal MM was 15.1 months (95%KI 4.5-25.7; all histologies). Multivariate analysis revealed gender, age, histological subtype, cell specific growing features (spindle cell type; papillary type), necrosis, hyaline plaques and proliferation marker Ki67 as independent prognostic factors (p Conclusion: The comprehensive, state-law embedded cancer registry NRW ensures the complete area-wide identification and collection of cancer patients’ course out of 18 million residents. In this very large study MM cell specific growing features and proliferation index could be identified as new independent markers of MM outcome.
恶性间皮瘤的临床和组织学分析——一项全面的全国性研究
背景:北威斯特伐利亚州(CR NRW)癌症登记处是一个以州法律为基础的前瞻性癌症登记处,包括所有诊断为癌症的州居民(NRW计数约为1。1800万居民)。方法:选取2010 ~ 2012年在北威州诊断并收集的所有MM病例(n=1199例)。232例包含不完整的数据集。在967例有效病例中,755例(78.1%)可见原始病理报告,468例(48.4%)包括免疫组织化学。结果:967例MM 796患者中,男性占82.3%,女性占171例(17.7%),其中81.8%在最后验证日已经患病。根据icd编码,885例(91.5%)患者为胸膜MM (C45.0), 72例(7.4%)为腹膜MM, 2例(0.2%)为心包MM, 8例(0.8%)为不同部位MM。组织学以上皮样生长为主(60.4%),其次为双相生长(13.4%)和肉瘤样生长(9.4%);16.8%的人生长模式不明确。胸膜MM的中位总生存期(OS)为12.4个月(95%KI为11.3-13.4;所有组织学),腹膜MM的OS为15.1个月(95%KI 4.5-25.7;所有组织学)。多变量分析显示性别、年龄、组织学亚型、细胞特异性生长特征(梭形细胞类型;结论:全面的、嵌入国家法律的癌症登记处NRW确保了1800万居民中完整的全区域癌症患者病程的识别和收集。在这项非常大规模的研究中,MM细胞特异性生长特征和增殖指数可以被确定为MM预后的新的独立标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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