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肺癌肉瘤:监测、流行病学和最终结果(SEER)分析。

Pulmonary Carcinosarcoma: A Surveillance, Epidemiology, and End Results (SEER) Analysis.

机构信息

Department of Solid Tumor Oncology and Investigational Therapeutics, Levine Cancer Institute, Atrium Health, Charlotte, NC.

Department of Cancer Biostatistics, Levine Cancer Institute, Atrium Health, Charlotte, NC.

出版信息

Clin Lung Cancer. 2020 Mar;21(2):160-170. doi: 10.1016/j.cllc.2019.07.001. Epub 2019 Jul 10.

DOI:10.1016/j.cllc.2019.07.001
PMID:31455596
Abstract

INTRODUCTION

Pulmonary carcinosarcoma (PC) is a rare malignant neoplasm composed of epithelial and mesenchymal components. It accounts for < 1% of thoracic cancers and is not fully understood. This study examined Surveillance, Epidemiology, and End Results (SEER) data to describe demographic and clinical characteristics of patients with PC and assessed survival outcomes by treatment modality and stage.

PATIENTS AND METHODS

SEER data were reviewed to identify patients diagnosed with primary PC (1973-2012). Overall survival (OS) and disease-specific survival (DSS) were analyzed by univariate/multivariable Cox proportional hazards models and Kaplan-Meier methods.

RESULTS

A total of 411 patients were included. Median age was 67 (range, 24-96) years. Disease stage at the time of initial diagnosis was known for 74.7% of the identified patients (307/411). Of these patients, 23.1% had localized disease. Survival was significantly better for patients with localized disease (OS: 31 vs. 6 months, P < .001; DSS: 54 vs. 8 months, P < .001). Additionally, patients who received surgery alone had significantly improved OS (20 months; P < .001) and DSS (32 months; P < .001) compared to patients who received combined surgery and radiotherapy (OS: 7 months; DSS: 8 months) or radiotherapy alone (OS: 4 months; DSS: 4 months).

CONCLUSION

Treatment with surgery alone resulted in superior survival outcomes compared to other treatment modality combinations, regardless of patient age and disease stage. Within the limitations of this study, providers may wish to consider these findings when devising patient treatment plans.

摘要

简介

肺肉瘤(PC)是一种罕见的恶性肿瘤,由上皮和间叶成分组成。它占胸部癌症的<1%,尚未完全了解。本研究通过监测、流行病学和最终结果(SEER)数据来描述 PC 患者的人口统计学和临床特征,并按治疗方式和分期评估生存结果。

患者和方法

回顾 SEER 数据,以确定 1973-2012 年间诊断为原发性 PC 的患者。通过单变量/多变量 Cox 比例风险模型和 Kaplan-Meier 方法分析总生存率(OS)和疾病特异性生存率(DSS)。

结果

共纳入 411 例患者。中位年龄为 67 岁(范围:24-96 岁)。74.7%(307/411)的患者在初始诊断时已知疾病分期。这些患者中,23.1%为局限性疾病。局限性疾病患者的生存明显更好(OS:31 个月 vs. 6 个月,P<.001;DSS:54 个月 vs. 8 个月,P<.001)。此外,与接受联合手术和放疗(OS:7 个月;DSS:8 个月)或单纯放疗(OS:4 个月;DSS:4 个月)的患者相比,仅接受手术治疗的患者的 OS(20 个月;P<.001)和 DSS(32 个月;P<.001)均显著改善。

结论

与其他治疗方式组合相比,单独手术治疗的生存结果更好,无论患者年龄和疾病分期如何。在本研究的限制范围内,医生在制定患者治疗计划时可能会考虑这些发现。

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