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新加坡的原发性肺淋巴上皮瘤样癌。

Primary pulmonary lymphoepithelioma-like carcinoma in Singapore.

作者信息

Tay Chee Kiang, Chua Yang Chong, Takano Angela, Min Chee Madeline Yen, Lim Wan-Teck, Lim Cindy, Koh Mariko Siyue

机构信息

Department of Respiratory and Critical Care Medicine, Singapore General Hospital, Singapore.

Division of Surgical Oncology, National Cancer Center, Singapore.

出版信息

Ann Thorac Med. 2018 Jan-Mar;13(1):30-35. doi: 10.4103/atm.ATM_304_17.

Abstract

BACKGROUND

Primary pulmonary lymphoepithelioma-like carcinoma (PPLELC) is a rare subtype of nonsmall cell lung cancer (NSCLC) predominantly reported in East Asia. We aimed to evaluate clinical characteristics, diagnosis, treatment, and prognosis of PPLELC in Singapore.

METHODS

Retrospective review of all patients diagnosed with PPLELC at our center between 2000 and 2014.

RESULTS

All 28 patients were Chinese, 67.9% were female, and the median age was 58 years (range37-76 years). Majority (89.3%) were never smokers and 53.6% asymptomatic at diagnosis. About 28.6% presented with Stage I/II disease, 25% had Stage III disease, and 46.4% had Stage IV disease. All patients with Stage I/II disease underwent lobectomy without adjuvant treatment. Four out of 7 patients with Stage III disease underwent surgery with or without adjuvant therapy while the rest received chemoradiation. Twelve out of 13 patients with Stage IV disease received chemotherapy with or without radiotherapy. At the end of 2016, survival data were available for all 28 patients. Two-year survival rates for Stage I/II, Stage III, and Stage IV disease were 100%, 85.7%, and 61.5%, respectively, while survival was 100%, 85.7%, and 9.6%, respectively, at five years.

CONCLUSION

The majority (46.4%) of patients presented with metastatic disease. For those with Stage I-III disease, 5-year survival for PPLELC was better than other NSCLC subtypes. Multimodality treatment including surgery could be considered in locally advanced disease. In Stage IV disease, it tended to approximate that of NSCLC.

摘要

背景

原发性肺淋巴上皮瘤样癌(PPLELC)是一种非小细胞肺癌(NSCLC)的罕见亚型,主要在东亚地区报道。我们旨在评估新加坡PPLELC的临床特征、诊断、治疗及预后。

方法

回顾性分析2000年至2014年在我们中心诊断为PPLELC的所有患者。

结果

28例患者均为华裔,67.9%为女性,中位年龄为58岁(范围37 - 76岁)。大多数(89.3%)为从不吸烟者,53.6%在诊断时无症状。约28.6%为Ⅰ/Ⅱ期疾病,25%为Ⅲ期疾病,46.4%为Ⅳ期疾病。所有Ⅰ/Ⅱ期疾病患者均接受肺叶切除术,未进行辅助治疗。7例Ⅲ期疾病患者中有4例接受了手术,有或无辅助治疗,其余患者接受了放化疗。13例Ⅳ期疾病患者中有12例接受了化疗,有或无放疗。到2016年底,所有28例患者均有生存数据。Ⅰ/Ⅱ期、Ⅲ期和Ⅳ期疾病的两年生存率分别为100%、85.7%和61.5%,而五年生存率分别为100%、85.7%和9.6%。

结论

大多数(46.4%)患者表现为转移性疾病。对于Ⅰ - Ⅲ期疾病患者,PPLELC的5年生存率优于其他NSCLC亚型。局部晚期疾病可考虑包括手术在内的多模式治疗。在Ⅳ期疾病中,其生存率倾向于接近NSCLC。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1f/5772105/293fc3e15da1/ATM-13-30-g001.jpg

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