Prognostic Effect of Lymphovascular Invasion on TNM Staging in Stage I Non-Small-cell Lung Cancer

被引:28
|
作者
Noma, Daisuke [1 ,2 ]
Inamura, Kentaro [3 ]
Matsuura, Yosuke [1 ]
Hirata, Yoshifumi [1 ]
Nakajima, Takuya [1 ]
Yamazaki, Hirotsugu [1 ]
Hirai, Yoshimitsu [1 ]
Ichinose, Junji [1 ]
Nakao, Masayuki [1 ]
Ninomiya, Hironori [3 ]
Mun, Mingyon [1 ]
Nakagawa, Ken [1 ]
Masuda, Munetaka [2 ]
Ishikawa, Yuichi [3 ]
Okumura, Sakae [1 ]
机构
[1] Japanese Fdn Canc Res, Canc Inst Hosp, Dept Thorac Surg Oncol, Tokyo, Japan
[2] Yokohama City Univ, Sch Med, Dept Surg, Yokohama, Kanagawa, Japan
[3] Japanese Fdn Canc Res, Canc Inst Hosp, Canc Inst, Div Pathol,Dept Pathol, Tokyo, Japan
基金
日本学术振兴会;
关键词
Adjuvant chemotherapy; Lung cancer; LVI; Outcome; TNM stage; BLOOD-VESSEL INVASION; FORTHCOMING 8TH EDITION; PATHOLOGICAL STAGE; LYMPHATIC VESSEL; ADJUVANT CHEMOTHERAPY; VASCULAR INVASION; CM; PROJECT PROPOSALS; URACIL-TEGAFUR; CARCINOMA;
D O I
10.1016/j.cllc.2017.06.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Using 660 consecutive patients with stage I nonesmall-cell lung cancer (NSCLC) and a Cox proportional hazards model, we examined the prognostic association of lymphovascular invasion in TNM staging of stage I NSCLC. We found that stage IA with vascular invasion and stage IB disease have equivalent prognostic outcomes, suggesting that stage IA with vascular invasion should be upstaged to stage IB in the TNM classification of NSCLC. Introduction: Lymphovascular invasion (LVI) is a known adverse prognostic factor for early-stage nonesmall-cell lung cancer (NSCLC). Nonetheless, the prognostic effect of LVI on TNM staging of stage I NSCLC remains inconclusive. We thus hypothesized that it might be better to upstage pathologic stage IA NSCLC with LVI to pathologic stage IB NSCLC. Patients and Methods: Using a Cox proportional hazards model, we examined the effect of LVI on disease-specific survival (DSS) in stage IA versus stage IB disease in 660 consecutive patients with stage I NSCLC (598 with adenocarcinoma, 62 with squamous cell carcinoma) who had undergone complete resection. Results: On univariable analysis of stage IA cases, vascular invasion (VI) was significantly associated with inferior DSS (univariable hazard ratio [HR], 3.39; 95% confidence interval [CI], 1.46-7.89; P = .005). In contrast, lymphatic invasion exhibited a tendency toward inferior DSS (univariable HR, 2.90; 95% CI, 0.97-8.66; P = .056). Multivariable analysis of DSS in stage IA cases identified VI as an independent significant prognostic factor (multivariable HR, 2.86; 95% CI, 1.58-5.18; P = .007). With VI, DSS was significantly poorer for stage IB than for stage IA patients without VI (univariable HR, 3.44; 95% CI, 1.67-7.09; P < .001). In contrast, no difference was observed between patients with stage IA and VI and stage IB patients (P = .97). Conclusion: The presence of VI independently and significantly affects DSS in patients with stage IA NSCLC. We found that stage IA with VI and stage IB disease had equivalent prognostic outcomes. Our results suggest that stage IA with VI should be upstaged to IB in the TNM classification of NSCLC.
引用
收藏
页码:E109 / E122
页数:14
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