Li Yuanyuan, Zhang Lili, Jiang Juan, Yang Huaping, Cao Liming, Gu Qihua, Li Min, Hu Chengping
Department of Respiratory Medicine, Xiangya Hospital of Central South University, Changsha 410008, China.
Zhongguo Fei Ai Za Zhi. 2015 Sep 20;18(9):537-42. doi: 10.3779/j.issn.1009-3419.2015.09.02.
Pulmonary sarcomatoid carcinoma is a rare histologic subtype of non-small cell lung cancer. The effective treatment for this disease has not well defined due to its extremely low morbidity. This study explores the clinicopathological characteristics and prognosis of 38 patients with PSC, so as to provide some clues for its diagnosis and treatment.
The study enrolled 38 patients with PSC that were diagnosed with histology or cytology in our hospital between January 2000 and December 2013. We retrospectively analyzed general clinical characteristics, smoking history, tumor size, TNM staging, pathology, immunohistochemistry, diagnostic method, treatment and prognosis. We used SPSS 19.0 statistical software and Kaplan-Meier method to analyze our data.
Patients in this study were aged from 26 to 76 years old (the median age was 57.5 years old). Among all of them, the male to female ratio was 4:1, and 81.6% of patients had smoking history. Cough and hemoptysis were the most common primary symptoms. The median survival was 21 months, while one-year survival rate, three-year survival rate and five-year survival rate were 68.4%, 31.6% and 18.4% respectively. Tumor size, TNM staging, distant metastasis and surgery therapy were associated with the prognosis of patients.
CONCLUSIONS: Patients with PSC present with no special symptoms generally. According to our study, factors that affect patients' prognosis include tumor size, TNM staging, distant metastasis and surgery. Complete resection is the key treatment for PSC patients, but comprehensive chemoradiotherapy needs further exploration in evidence-based medicine. Biological target therapy may give new insight into treatment for PSC. .
肺肉瘤样癌是一种罕见的非小细胞肺癌组织学亚型。由于其发病率极低,该疾病的有效治疗方法尚未明确界定。本研究探讨38例肺肉瘤样癌患者的临床病理特征及预后,以便为其诊断和治疗提供一些线索。
本研究纳入2000年1月至2013年12月期间在我院经组织学或细胞学诊断为肺肉瘤样癌的38例患者。我们回顾性分析了患者的一般临床特征、吸烟史、肿瘤大小、TNM分期、病理、免疫组化、诊断方法、治疗及预后。我们使用SPSS 19.0统计软件和Kaplan-Meier方法分析数据。
本研究中的患者年龄在26岁至76岁之间(中位年龄为57.5岁)。其中,男女比例为4:1,81.6%的患者有吸烟史。咳嗽和咯血是最常见的主要症状。中位生存期为21个月,而1年生存率、3年生存率和5年生存率分别为68.4%、31.6%和18.4%。肿瘤大小、TNM分期、远处转移和手术治疗与患者的预后相关。
肺肉瘤样癌患者一般无特殊症状。根据我们的研究,影响患者预后的因素包括肿瘤大小、TNM分期