Methods: A total of 687 patients (636 males, 51 females; mean age 60.8±9.1 years; range 29 to 82 years) who were performed anatomical resection with the diagnosis of non-small cell lung cancer between January 2005 and December 2011 were analyzed retrospectively. Patients with or without bronchoscopically detected endobronchial lesion were divided into two groups. The two groups were compared in terms of having or not having hilar or ipsilateral mediastinal lymph node metastasis.
Results: As a result of an evaluation with chi-square analysis performed on patient groups with (n=174) or without (n=513) endobronchial lesion, we detected a significant correlation between the presence of endobronchial lesion and hilar lymph node metastasis status (p=0.014), while we did not detect a significant correlation between the presence of endobronchial lesion and ipsilateral mediastinal lymph node metastasis status (p=0.383). Five-year survival in patients with or without endobronchial lesion was 58.6% and 40.2%, respectively, with a statistically significant correlation (p<0.001).
Conclusion: Hilar lymph node metastasis is significantly more frequently observed in non-small lung cancer cases with endobronchial lesion. This fact raises the suspicion that metastasis may develop via the peribronchial lymphatics.
Lung cancer is diagnosed in metastatic phases or locally late stages due to its natural course, thus surgical treatment is not an option in 70% of the patients.[4] The stage of the disease is the most important factor of the prognosis and treatment.[5] The tumor, node and metastasis staging system puts forth the spreading of the cancer by evaluating factors such as tumor size and invasion, lymphatic invasion and presence of metastatic disease.[6] Mediastinal lymph node metastasis is one of the most important criteria in determining the prognosis of lung cancer. Therefore, in this study, we aimed to evaluate whether or not there is a relationship between endobronchial lesion (EBL) and hilar and/or mediastinal lymph node metastasis in NSCLC.
Statistical analysis
Statistical Package for the Social Sciences (SPSS)
version 16.0 (SPSS Inc., Chicago, IL, USA) software
program was used in the analysis of the data. Suitability of the quantitative data for normal distribution was
analyzed with Kolmogorov-Smirnov test and parametric
methods were used in the analysis of the variables with
normal distribution and homogenous variance and nonparametric
methods were used for the other variables.
Independent t and Mann-Whitney U tests were used to
compare independent groups. Partial correlation test was
used to analyze the correlations of the variables after the
quantitative data were controlled with the main factor.
Pearson and chi-square tests were used to compare
the categorical data and logistic regression analysis
was used to identify the cause and effect relationship
between the explanatory variables in dual (diotom)
and multiple (multinominal) categories. Kaplan-Meier
(product limit method) analysis was used to analyze
the effects of factors on mortality and life time and
Cox regression analysis was used to measure the effects
of the prognostic variables on life time compared to
the main factor. The quantitative data were expressed
as mean±standard deviation and median±interquartile
range values and the categorical data were expressed
as number (n) and percentages (%) in the tables. The
data were analyzed in a 95% confidence interval and a
p value less than 0.05 was accepted as significant.
Table 1: Characteristics of patients with or without endobronchial lesions
Our series included 380 (55.32%) squamous cell carcinomas (SCCs), 238 (34.65%) adenocarcinomas, 50 (7.27%) large cell carcinomas and 19 (2.76%) other non-small cell lung carcinomas. The presence of EBLs in SCC was significantly more frequent (p<0.001) compared to adenocarcinoma (p<0.001). In the general group, the median survival was 52.1 months in SCC, 51.5 months in adenocarcinoma, and 54.72 months in large cell carcinoma, without a statistically significant difference (p=0.592).
Pathological stage distribution of patients revealed that 155 (22.56%) were stage 1A, 134 (19.5%) were stage 1B, 127 (18.49%) were stage 2A, 146 (21.25%) were stage 2B, and 125 (18.2%) were stage 3A. The frequency of EBLs was statistically significantly increased in stage 3A (p=0.006).
According to the distribution of lymph node status (N), 491 patients (71.47%) were in N0, 100 (14.55%) were in N1, and 96 (13.97%) were in N2 groups. There was a significant increase in the frequency of pathological N1 in the presence of EBL (p=0.014), whereas no such correlation was detected for N2 (p=0.383). W hen t he survival in general group of patients was evaluated by taking the N factor into account, median survival time was 58.8 months in N0, 49.2 months in N1, and 39.7 months in N2 groups (Table 2). The survival time was statistically significantly better in the presence of EBLs in N0 and N1 groups (p=0.007). The survival median was better in the presence of EBLs in N2 group, without any statistical significance.
The anatomical resections performed on the patients were divided into two groups as lobectomy and pneumonectomy. There were 117 patients (17.03%) in the pneumonectomy group and 570 patients (82.97%) in the lobectomy group. The frequency of pneumonectomy was significantly increased in patients with EBLs (p<0.001).
Table 2: Five-year survival analyses of lymph node status
Five-year survival rate in the general group was 45.6%. Median life time was 55.5 months in general; 50.4 months in patients without EBL and 65.4 months in patients with EBL. The five-year survival was 40.2% in patients without EBL and 58.6% in patients with EBL. The difference in survival rates between both groups was statistically significant (p<0.001).
In previous studies, other controversial issues included tumor localizations that metastasized to the lymph nodes more, and whether or not these metastases were more hilar or mediastinally located. Ito et al.[10] reported that even though lymph node metastasis was seen more in peripheral tumors, there was no statistically significant difference from the central tumors (p=0.124). On the other hand, Krdzalic et al.[8] stated that N1 metastasis was significantly more frequent in central tumors. Furthermore, Marra et al.[11] analyzed 535 patients with N1 metastasis and observed that N1 metastasis was more frequent in central tumors (p<0.001). These findings support our study. Moreover, Graham et al.[9] showed that lymph node metastasis rate increased as the tumors moved from peripheral to central areas. As the localization of the tumor distanced from peripheral, segmental, bronchial, or lobar bronchial to main bronchial, the rate of lymph node metastasis was found to be 27%, 42%, 68% and 73%, respectively, and statistically significant.[9] In this study, it was demonstrated that in central tumors, both N1 a nd N 2 metastases were significantly more frequent.[9] In our study, we determined that both N1 and N2 metastases were increased in tumors with EBLs. The increase in N1 metastasis was statistically significant, whereas the increase in N2 metastasis was not. These results support our hypothesis that the tumor may metastasize more frequently to the hilar regional lymph nodes via the peribronchial lymphatics in the presence of EBL.
Another important aim of our study was to analyze the difference between prognosis and survival in peripherally and centrally located tumors. Ketchedjian et al.[7] showed that the median survival in central and peripheral tumors was 18 and 39 months, respectively, with a statistically significant difference. In another study, five-year survival rate in central and peripheral tumors was 38% and 45%, respectively, with no statistically significant difference.[11] In addition, Ito et al.[10] found that the five-year survival rates were better in central tumors compared to peripheral tumors. In this study, five-year survival in central and peripheral tumors was 51.5% and 21.2%, respectively, with a statistically significant difference in favor of central tumors (p=0.034). Our findings support the results of this study. When general survival and N were compared in our study, survival was better in the presence of EBLs.
As known, adenocarcinomas tend to be more peripherally whereas SCCs tend to be more centrally located.[12] A study performed by Uslu et al.[13] supported this. Squamous cell carcinoma is seen more in the bronchoscopically detected vegetating lesions or tumoral infiltrations.[13] In their study, Watanabe et al.[14] showed that the majority of the histological types of peripheral tumors were adenocarcinomas. In a study by Brooks et al.,[15] the frequency of SCCs was found to be increasing in central tumors. In our study, SCC was seen more than adenocarcinoma in endobronchial tumors (85.6% vs. 9.8%) and the difference in between was statistically significant. In peripheral tumors, adenocarcinoma incidence was 37.4% and SCC incidence was 45%, and although not statistically significant, there was a dominance of SCC.[16] According to the literature, adenocarcinoma incidence is higher in females.[17] We detected that the incidence of EBL was significantly lower in females.
Another condition that may affect survival is tumor type. A great number of studies have demonstrated that the survival of patients with SCCs is better than those with adenocarcinomas. Similarly, Carbone et al.[16] detected that five-year survival probability in SCCs was better than adenocarcinomas (48.8% and 40.9%, respectively). Also, in another study, five-year survival in SCC was better than adenocarcinoma.[19] However, a review of the literature revealed that the effect of histological type on survival is still controversial.[18] Considering our overall patient population, the fiveyear survival of patients with SCCs was 38.6%, whereas it was 33.6% in those with adenocarcinomas, with no statistically significant difference. In our study, there was a significant difference between the presence and absence of EBL in terms of survival. For this reason, even though SCC was seen more in patients with EBLs, we think that the difference between the survivals does not depend on it.
To our knowledge, our study is the largest series about the relationship between endobronchial lesions and lymph node metastasis in Turkey. However, it has several limitations including being a retrospective and single-center study, thus providing a limited contribution to other staging studies.
In conclusion, N1 positivity was significantly more frequent in non-small cell lung cancer cases with endobronchial lesions, which raises the suspicion that metastasis may develop via the peribronchial lymphatics. Also, since we showed that the survival of patients with endobronchial lesions was much better than those with peripheral tumors, the presence of endobronchial component may be shown in good prognostic factors. However, further clinical studies are needed to clarify this issue.
Declaration of conflicting interests
The authors declared no conflicts of interest with respect to
the authorship and/or publication of this article.
Funding
The authors received no financial support for the research
and/or authorship of this article.
1) Wilkins EW, Urschel HC. General Thoracic Surgery: History
and Development. In: Pearson FG, Cooper JD, editors. Thoracic
Surgery. Philadelphia: Churchill Livingstone; 2002. p. 1-8.
2) Shields TW. The significance of ipsilateral mediastinal lymph
node metastasis (N2 disease) in non-small cell carcinoma of the
lung. A commentary. J Thorac Cardiovasc Surg 1990;99:48-53.
3) Casali C, Stefani A, Morandi U. N1 non-small-cell lung
cancer. A 20-year surgical experience. Asian Cardiovasc
Thorac Ann 2011;19:217-24.
4) Scagliotti G. Symptoms, signs and staging of lung cancer.
Eur Respir Mon 2001;17:86-119.
5) Yılmaz HÖ, Saygı A, Sarıman N, Maraşlı D, Düzgün Y,
Köksal H. Relationship of T-stage and nodal metastases
according to the up-to-date clinical TNM staging in lung
cancer. Turk Gogus Kalp Dama 2012;20:101-6.
6) Sihoe AD, Yim AP. Lung cancer staging. J Surg Res
2004;117:92-106.
7) Ketchedjian A, Daly BD, Fernando HC, Florin L, Hunter
CJ, Morelli DM, et al. Location as an important predictor of
lymph node involvement for pulmonary adenocarcinoma. J
Thorac Cardiovasc Surg 2006;132:544-8.
8) Krdzalic G, Mesic D, Iljazovic E, Brkic S, Krdzalic A,
Ramic N, et al. Mediastinal lymph node metastasis pattern
in clinically N0 non-small-cell lung cancer patients who
underwent surgical resection. Med Arh 2010;64:332-4.
9) Graham AN, Chan KJ, Pastorino U, Goldstraw P. Systematic
nodal dissection in the intrathoracic staging of patients
with non-small cell lung cancer. J Thorac Cardiovasc Surg
1999;117:246-51.
10) Ito M, Yamashita Y, Miyata Y, Ohara M, Tsutani Y, Ikeda
T, et al. Prognostic impact of the primary tumor location
based on the hilar structures in non-small cell lung cancer
with mediastinal lymph node metastasis. Lung Cancer
2012;76:93-7.
11) Marra A, Hillejan L, Zaboura G, Fujimoto T, Greschuchna
D, Stamatis G. Pathologic N1 non-small cell lung cancer:
correlation between pattern of lymphatic spread and
prognosis. J Thorac Cardiovasc Surg 2003;125:543-53.
12) Tateishi M, Fukuyama Y, Hamatake M, Kohdono S, Ishida
T, Sugimachi K. Skip mediastinal lymph node metastasis in
non-small cell lung cancer. J Surg Oncol 1994;57:139-42.
13) Uslu Ö, Günaçtı E, Tuksavul F, Gülpek M, Vatansever T,
Güçlü S. The relationship of endobronchial appearance with
histopathological sub-type in lung cancer. İzmir Göğüs
Hastanesi Dergisi 2005;19:1-5.
14) Watanabe Y, Murakami S, Oda M, Ohta Y, Watanabe S,
Nozaki Z, et al. Surgical management of early stage central (hilar) and peripheral nonsmall cell lung carcinoma. Cancer
2000;89:2438-44.
15) Brooks DR, Austin JH, Heelan RT, Ginsberg MS, Shin V,
Olson SH, et al. Influence of type of cigarette on peripheral
versus central lung cancer. Cancer Epidemiol Biomarkers
Prev 2005;14:576-81.
16) Carbone E, Asamura H, Takei H, Kondo H, Suzuki K,
Miyaoka E, et al. T2 tumors larger than five centimeters
in diameter can be upgraded to T3 in non-small cell lung
cancer. J Thorac Cardiovasc Surg 2001;122:907-12.
17) Okamoto T, Maruyama R, Suemitsu R, Aoki Y, Wataya H,
Kojo M, et al. Prognostic value of the histological subtype
in completely resected non-small cell lung cancer. Interact
Cardiovasc Thorac Surg 2006;5:362-6.