Primary signet ring cell histology does not portend worse survival for early stage lung cancer following lobectomy

被引:1
|
作者
Peng, Terrance [1 ]
Yau, Anita [2 ]
Ding, Li [2 ]
David, Elizabeth A. [1 ]
Wightman, Sean C. [1 ]
Atay, Scott M. [1 ]
Kim, Anthony W. [1 ]
机构
[1] Keck Sch Med USC, Dept Surg, Div Thorac Surg, Los Angeles, CA USA
[2] Keck Sch Med USC, Dept Prevent Med, Los Angeles, CA USA
来源
关键词
lung adenocarcinoma; signet ring cell carcinoma; thoracic surgery; thoracic neoplasms; ADENOCARCINOMA;
D O I
10.1177/02184923211045910
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Signet ring cell (SRC) histology is considered a poor prognostic factor in various cancers. However, primary SRC lung adenocarcinoma is rare and poorly understood. Methods The National Cancer Database was queried to identify treatment-naive patients who received lobectomy for primary SRC or non-SRC pT1-2N0 lung adenocarcinoma <4 cm within four months of diagnosis. SRC lung adenocarcinoma was defined by ICD-O-3 code 8490, while non-SRC lung adenocarcinoma was defined by ICD-O-3 codes 8140, 8141, 8143, 8147, 8255, 8260, 8310, 8481, 8560, and 8570-8574. The Kaplan-Meier curve and log-rank test was used to compare five-year OS between SRC versus non-SRC lung adenocarcinoma cohorts. The impact of SRC histology on risk of death was assessed using the Cox proportional hazards regression model. Results 48,399 patients were included in this study: 62 with primary SRC lung adenocarcinoma and 48,337 with non-SRC lung adenocarcinoma. The mean age of the overall cohort was 67.0 +/- 9.6 years. Five-year OS following lobectomy did not differ significantly between SRC lung adenocarcinoma and non-SRC lung adenocarcinoma cohorts (SRC 73.9% vs. non-SRC 69.3%, p = 0.64). SRC histology did not significantly impact risk of death within five years after lobectomy (HR 0.89, p = 0.66). Conclusions Following lobectomy for pT1-2N0 tumors <4 cm, patients with primary SRC lung adenocarcinoma do not experience worse five-year OS or increased risk of death within five years relative to those with non-SRC lung adenocarcinoma. Additional study, including exploration of emerging molecular profiling data, may serve to better define optimal treatment for this histopathologic group of lung adenocarcinomas.
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收藏
页码:185 / 189
页数:5
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