Lymphangiosis carcinomatosa independently affects long-term survival of Non-Small Cell Lung Cancer patients

被引:3
作者
Heldwein, Matthias B. [1 ]
Doerr, Fabian [1 ]
Schlachtenberger, Georg [1 ]
Menghesha, Hruy [1 ]
Kuhn, Elmar W. [1 ]
Scheel, Andreas H. [2 ]
Michel, Maximilian [3 ]
Wahlers, Thorsten [1 ]
Hekmat, Khosro [1 ]
机构
[1] Univ Hosp Cologne, Dept Cardiothorac Surg, Cologne, Germany
[2] Univ Hosp Cologne, Inst Pathol, Cologne, Germany
[3] Univ Cologne, Fac Math & Nat Sci, Inst Zool, Cologne, Germany
来源
SURGICAL ONCOLOGY-OXFORD | 2021年 / 37卷
关键词
Lung cancer; NSCLC; Lymphangiosis carcinomatosa; Survival; Prognosis; Risk factor; LYMPH-NODE METASTASIS; TNM CLASSIFICATION; PROGNOSTIC-FACTORS; AMERICAN-COLLEGE; STAGING PROJECT; 8TH EDITION; INVASION; METAANALYSIS; RESECTION; COLON;
D O I
10.1016/j.suronc.2021.101611
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The significance of postoperatively diagnosed Lymphangiosis Carcinomatosa (L1) as an independent risk factor for long-term survival in Non-Small Cell Lung Cancer (NSCLC) remains controversial. We analyzed the effect of L1 on postoperative survival in stage I, II and III NSCLC-patients. Methods: We investigated all consecutive patients with NSCLC between January 2012 and December 2019 who underwent an anatomical resection and radical lymphadenectomy at our institute. L1-were compared to L0patients. All patients received adjuvant chemotherapy in accordance with European guidelines. 3- and 5- year survival rates and median-survival were assessed. To investigate whether L1 is an independent risk factor, we carried out a multivariate cox regression and a pair-match analysis looking at different properties such as TNM. Results: A total of 641 patients (L0: 74%; L1: 26%) were analyzed. Baseline characteristics were comparable between groups. The mean age was 65.3 +/- 10.2 years and 64.9 +/- 9.4 years in the L0 and L1-groups respectively (p-value = 0.703). 58.5% of L0-patients were male (L1: 62.7%; p-value = 0.351). Overall survival in the L1group was significantly shorter compared to the L0-group (L1: 42.3 +/- 2.8; L0: 67.6 +/- 2.1 months; p-value<0.0001). We confirmed this finding in a pair-matched analysis (L0: 73.9 +/- 4.7 months; L1: 42.2 +/- 4.2; pvalue = 0.009). 3- and 5-year survival were significantly shorter for L1-patients (3-year: L0: 65.9%; L1: 35.9%; pvalue<0.0001) (5-year: L0: 34.9%; L1: 7.5%; p-value<0.0001). Conclusion: L1 is an independent risk factor for long-term survival of patients with NSCLC. This cohort supports that the L0/L1 status should be included in pathological reports. We suggest to further include L0/L1-status in guideline recommendations for NSCLC patients.
引用
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页数:6
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