Suppr超能文献

国家恶性胸膜间皮瘤的流行病学趋势:国家癌症数据库研究。

National Trends in the Epidemiology of Malignant Pleural Mesothelioma: A National Cancer Data Base Study.

机构信息

Division of General Thoracic Surgery, Mayo Clinic, Rochester, Minnesota.

Division of General Thoracic Surgery, Mayo Clinic, Rochester, Minnesota.

出版信息

Ann Thorac Surg. 2018 Feb;105(2):432-437. doi: 10.1016/j.athoracsur.2017.09.036. Epub 2017 Dec 7.

Abstract

BACKGROUND

Malignant pleural mesothelioma (MPM) remains an aggressive malignancy that is difficult to cure. However, the treatment paradigm of MPM has evolved, and the national practice patterns are unknown. This study examined the national trends in the epidemiology, national treatment patterns, and survival of patients with this disease.

METHODS

We identified all patients (n = 19,134) with MPM from the National Cancer Data Base from 2004 to 2013. We analyzed patient, tumor characteristics, and treatment patterns using descriptive statistics and used Kaplan-Meier and Cox proportional hazards models to estimate survival stratified by the type of therapy administered.

RESULTS

Four histologic subtypes were represented in the National Cancer Data Base, these included sarcomatoid (n = 2,355 [12.3%]), epithelioid (n = 6,858 [35.8%]), biphasic (n = 13,617 [11%]), and not otherwise specified (n = 8,560 [44.7%]). Across all subtypes, the prevalence of mesothelioma was highest among white men. Sarcomatoid had the worst survival (adjusted hazard ratio, 2.2; p < 0.001). Most patients did not receive any specific modality of treatment (40.2%). Chemotherapy alone was the most common treatment used (31.8%). Trimodality treatment with chemotherapy, surgical resection, and radiation therapy was associated with the best survival (adjusted hazard ratio, 0.43; p < 0.001), followed by combination chemotherapy and resection (adjusted hazard ratio, 0.49; p < 0.001).

CONCLUSIONS

This is the first publication to date to analyze the mesothelioma National Cancer Data Base. Although survival remains poor, multimodality therapy with surgical resection is associated with the best survival for MPM. Further research is needed to improve survival and overall patient outcomes.

摘要

背景

恶性胸膜间皮瘤(MPM)仍然是一种难以治愈的侵袭性恶性肿瘤。然而,MPM 的治疗模式已经发展,国家的治疗模式尚不清楚。本研究检查了这种疾病的流行病学、国家治疗模式和患者生存的全国趋势。

方法

我们从 2004 年至 2013 年从国家癌症数据库中确定了所有 MPM 患者(n=19134)。我们使用描述性统计分析了患者、肿瘤特征和治疗模式,并使用 Kaplan-Meier 和 Cox 比例风险模型估计了按治疗类型分层的生存情况。

结果

国家癌症数据库中包含四种组织学亚型,包括肉瘤样型(n=2355[12.3%])、上皮样型(n=6858[35.8%])、双相型(n=13617[11%])和未特指型(n=8560[44.7%])。在所有亚型中,间皮瘤的患病率在白人男性中最高。肉瘤样型的生存最差(调整后的危险比,2.2;p<0.001)。大多数患者未接受任何特定的治疗方式(40.2%)。单独化疗是最常用的治疗方法(31.8%)。化疗、手术切除和放疗的三联疗法与最佳生存相关(调整后的危险比,0.43;p<0.001),其次是联合化疗和切除术(调整后的危险比,0.49;p<0.001)。

结论

这是迄今为止第一篇分析间皮瘤国家癌症数据库的出版物。尽管生存仍然较差,但手术切除的多模式治疗与 MPM 的最佳生存相关。需要进一步研究以改善生存和整体患者结局。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验