ATS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


  Click here to read this article as a CME activity


Ann Thorac Surg 2008;86:1626-1630. doi:10.1016/j.athoracsur.2008.07.076
© 2008 The Society of Thoracic Surgeons

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
Panagiotis Misthos
Evangelos Sepsas
John Kokotsakis
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Misthos, P.
Right arrow Articles by Lioulias, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Misthos, P.
Right arrow Articles by Lioulias, A.
Related Collections
Right arrow Lung - cancer
Right arrowRelated Article


Original Articles: General Thoracic

The Significance of One-Station N2 Disease in the Prognosis of Patients With Nonsmall-Cell Lung Cancer

Panagiotis Misthos, MD, PhDa,*, Evangelos Sepsas, MD, PhDb, John Kokotsakis, MDa, Ion Skottis, MDb, Achilleas Lioulias, MD, PhDa

a Thoracic Surgery Department, Sismanogleio General Hospital, Athens, Greece
b Thoracic Surgery Department, General Hospital for Chest Diseases "Sotiria," Athens, Greece

Accepted for publication July 28, 2008.

* Address correspondence to Dr Misthos, 16-18A Markou Avgeri St, 15343 Agia Paraskevi, Athens, Greece (Email: panmisthos{at}yahoo.gr).


General thoracic surgery: The Annals of Thoracic Surgery CME Program is located online at http://cme.ctsnetjournals.org. To take the CME activity related to this article, you must have either an STS member or an individual non-member subscription to the journal.

 

    Abstract
 Top
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 
Background: A retrospective study was conducted to define the characteristics and the prognosis of N2 disease subgroups according to their patterns of spread.

Methods: From January 1993 to December 2004, 1,329 patients underwent lung resection for bronchogenic carcinoma The records of all patients with positive mediastinal lymph nodes at the surgical specimen (pIIIA/N2) after radical resection were analyzed, and the pattern of mediastinal lymphatic spread was classified according to regional spread, to skip metastasis, and to one or two or more lymph node stations, in relation to primary tumor location. Age, sex, type of resection, right or left lesion, T status, primary tumor location, tumor size, tumor central or peripheral location, histology, and survival were recorded and analyzed. Survival was analyzed according to regional spread or not, number of mediastinal lymph node stations involved, and skip metastasis status.

Results: Among 302 cases (22.7%) with positive mediastinal lymph nodes pIIIA/N2, 66 (22%) were skip metastases, 72 (24%) had a nonregional mode of spread, and 199 (66%) included two or more stations of mediastinal lymph node invasion. Cox regression analysis of all cases disclosed malignant invasion in only one mediastinal lymph node station as the only favorable factor of survival (p < 0.001, odds ratio 0.57, 95% confidence interval: 0.42 to 0.78).

Conclusions: The presence of one-station mediastinal lymph node metastasis in patients with nonsmall-cell lung cancer who underwent major lung resection with complete mediastinal lymph node dissection proved to be a good prognostic factor that should be taken into account in the future.

The presence or absence of lymph node metastasis is the single most important factor for estimating the possibility of disease recurrence and prognosis in surgical treatment of nonsmall-cell lung cancer (NSCLC). The typical pattern of the lung's lymphatic drainage suggests a linear model of dissemination malignancy initiating from the tumor, spreading to intrapleural lymph nodes and then to hilar ones (N1). The next station is the ipsilateral mediastinal lymph nodes in a downstream manner, namely, from the closer nodes to the hilum to the most distant [1]. In extremis, the contralateral mediastinal and the extrathoracic lymph nodes are involved (N3). However, great variability exists concerning the patterns of lymphatic drainage from bronchopulmonary segments to mediastinal lymph nodes. The patterns of spread include nonregional or skip metastasis as well as involvement of one, two, or more mediastinal lymph node stations.

Although several studies have been published during the last few years [2–6], the exact incidence, the clinical significance, and the oncologic interpretation of the different ways of lymphatic spread to the mediastinum remain to be clarified. The authors conducted a retrospective study on a fairly large population to determine the impact on survival of the pattern of NSCLC spread to the mediastinal lymph nodes among patients who underwent major lung resection.


    Material and Methods
 Top
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 
From January 1993 to December 2004, 1,329 patients underwent lung resection for bronchogenic carcinoma pathologically staged as pI–IIIA. The Scientific and Ethics Committee of Sismanogleio General Hospital has approved the conduction of the study. Individual consent for the study was waived.

This group included 1,077 men (81%) and 252 women (19%), aged 44 tp 78 years (median, 62). The types of resection included 372 pneumonectomies (27.9%), 219 right (59%) and 153 left (41%), and 957 lobectomies (72.1%). The patients were staged preoperatively by different means of chest imaging (radiography, computed tomography, magnetic resonance imaging) and invasive procedures (medistinoscopy, anterior mediastinotomy, and so forth). Positron emission tomography scan was not available. The findings of pathologic staging consisted of 90 cases (6.7%) with pIA/B, 213 (16%) with pIIA, 699 (52.7%) with pIIB, and 327 (24.6%) with pIIIA. All pIIIA/N2 cases were due to unsuspected N2 disease. Thus, no patient had induction therapy. All patients with N2 disease received platinum-based adjuvant therapy.

The records of all patients with NSCLC with positive mediastinal lymph nodes at the surgical specimen (pIIIA/N2) after radical resection were analyzed. Complete resection was defined as removal of the primary tumor and all accessible hilar and mediastinal lymph nodes, with no residual tumor left behind (resection of all macroscopic tumor and resection margins free of tumor at microscopic analysis). All patients underwent standard resections (lobectomy, bilobectomy, or pneumonectomy). Patients who underwent minor resections were excluded from the study. A complete mediastinal lymphadenectomy was routinely performed. The following lymph nodes compartments were routinely dissected: superior mediastinal and paratracheal on the right side; aortopulmonary window and preaortic on the left side, subcarinal and lower mediastinal on both sides. Left paratracheal nodes were not routinely included in the dissection. Only palpable lymph nodes in this region were surgically removed when encountered.

Age, sex, type of resection, right or left lesion, T status, primary tumor location, tumor size, tumor central or peripheral location, histology, and survival were recorded and analyzed. Mediastinal lymph node involvement was classified as upper or lower level and was grouped according to primary tumor location. All patients were postsurgically staged according to the 1997 TNM classification [7]. Lymph node levels were classified according to the American Thoracic Society system [8].

Hence, upper mediastinal lymph nodes were 1, 2, 3, 4, 5, and 6; and lower mediastinal lymph nodes were 7, 8, and 9.

Furthermore, the pattern of mediastinal lymphatic spread was classified according to regional spread, to skip metastasis, and to one, two, or more lymph node stations, in relation to primary tumor location.

Several studies [5, 6, 9, 10] have showed that the location of the primary tumor corresponds to the mediastinal areas where lymph nodes are likely to be diseased. The corresponding areas were the upper mediastinum for right upper lobe lesions, lower mediastinum for right lower lobe lesions, and subaortic component (levels 4 through 6) and lower mediastinum for left lower lobe lesions. If a tumor was located in more than one lobe, the main location of where the tumor appeared to start (where it was predominantly located) was considered its lobe of origin. In this way, every tumor was assigned as originating from only one lobe. Therefore, regional spread was defined for upper lobe tumors as invasion to levels 1 through 6, and for lower lobe tumors to levels 7 through 9.

Skip metastasis was defined as the presence of mediastinal lymph node metastasis without intralobar, scissural, or hilar lymph node involvement (N2 without N1).

Survival analysis referred to the 3-year survival rate, because the study has not matured for 5-year survival estimation. Survival was studied according to right or left lesion and primary tumor location. Moreover, survival was analyzed according to regional spread or not, number of mediastinal lymph node stations involved, and skip metastasis status.

Frequencies were compared with the {chi}2 test for categorical variables; Fisher's exact test was used for small samples. Survival was calculated by the Kaplan-Meier method; it included all cancer-related deaths and excluded all postoperative ones. The deaths for causes other than the tumor and postoperative deaths were considered as withdrawals, the date of death representing the endpoint of follow-up. Multivariate Cox regression was used to test the relationship of survival to mode of spread to the mediastinal lymph nodes. Age, sex, type of resection, right or left lesion, histology, nonregional spread, skip metastasis, and spread to two or more lymph node stations were matched in a multivariate analysis. A p value less than 0.05 was treated as significant.


    Results
 Top
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 
Patients at stage pIIIA/N2 were the target group to be studied. This group consisted of 302 patients (22.7%). The demographic and clinicopathologic characteristics of this group are fully described in Table 1.


View this table:
[in this window]
[in a new window]

 
Table 1 Demographic Data and Oncologic Characteristics
 
The incidence of mediastinal lymph node involvement according to primary tumor location was studied (Table 2). In 59% of the cases, the upper mediastinal lymph nodes were invaded, 22.5% of the lower ones and 18.5% of both the upper and lower lymph node stations. Positive lymph nodes belonged to the upper mediastinal group when the primary tumor was located at right or left upper lobes, whereas tumors of right middle, right lower, and left lower lobe metastasize more often to the lower one. Apart from the right upper lobe (12.6%), all other lobar locations of the primary tumor disclosed almost the same tendency (18% to 26%) to mestasize to both upper and lower mediastinal lymph nodes.


View this table:
[in this window]
[in a new window]

 
Table 2 Lymph Node Involvement According to Primary Tumor Location
 
Among 302 cases with positive mediastinal lymph nodes, 66 were skip metastases (22%), 72 had a nonregional mode of spread (24%), and 199 (66%) cases included two or more stations of mediastinal lymph node invasion (Table 3). Skip metastases were more frequently found in tumors of the right upper lobe. Nonregional mode of spread was more common among the tumors of the left lower lobe. Tumors of the right middle and lower lobe metastasize more easily to more than two mediastinal lymph node stations. One-station involvement cases included 16 cases of skip metastasis (15.5%) and 21 cases of nonregional spread (20%).


View this table:
[in this window]
[in a new window]

 
Table 3 Mode of Spread in Mediastinal Lymph Nodes
 
Univariate analysis of 3-year survival rates (Table 4) disclosed better survival after skip metastasis (p = 0.027), regional lymph node spread (p = 0.047), and one-station invasion (p < 0.001) (Fig 1). Skip metastasis and regional lymph node spread had improved survival rates for patients with right-sided tumors (p = 0.003 and p = 0.046, respectively). The number of stations of mediastinal lymph node metastasis seemed to influence survival of both right- and left-sided tumors (p = 0.004 and p = 0.002, respectively). Lobe-specific survival analysis revealed that skip metastasis, regional lymph node invasion, and one-station metastasis were statistically significant favorable factors for survival only for right upper lobe tumors (p = 0.001, p = 0.024, p < 0.001, respectively).


View this table:
[in this window]
[in a new window]

 
Table 4 Three-Year Survival Rates According to Mode of Spread in Mediastinal Lymph Nodes
 

Figure 1
View larger version (17K):
[in this window]
[in a new window]

 
Fig 1. Kaplan-Meier plots and life tables of regional (squares), skip (diamonds), and one-station (triangles) mode of spread (3-year survival).

 
Cox regression analysis (Table 5) of all cases disclosed malignant invasion in only one mediastinal lymph node station as the only independent favorable factor of survival (p < 0.001, odds ratio 0.57, 95% confidence interval: 0.42 to 0.78).


View this table:
[in this window]
[in a new window]

 
Table 5 Cox Regression Analysis Results
 

    Comment
 Top
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 
One should not take for granted that cancer lymphatic spread follows a linear model from intraparenchymal nodes to hilar, mediastinal, and extrathoracic ones. The lymphatic network draining the lung is extensive and variability is probably the rule. Riquet and colleagues [11] have reported direct lymph passages from each lobe to the mediastinum. More commonly, these communications were observed in the upper lobes. This provides multiple pathways for dissemination, creating a complicated model to be used for clinical assessment. It is wise not to underestimate the genetic profile of the primary tumor, which might keep a central role to the mode of tumor's lymphatic spread [12].

Surgical resection remains the cornerstone of management for NSCLC. Among other factors, the prognosis of these patients depends on metastasis to the lymph nodes, especially the ipsilateral (N2) or contralateral (N3) mediastinal lymph nodes [13–15]. Nonsmall-cell lung cancer with N2 lymph nodes positive for metastases (approximately 20% to 40% of all patients with NSCLC) shows extremely low survival rates. Preoperative staging detecting positive N2 lymph nodes renders surgical resection not useful, and these patients should be given neoadjuvant therapy and reconsidered for surgical treatment [16, 17]. Most clinicians dealing with thoracic oncology agree that patients who have NSCLC with ipsilateral mediastinal lymph node (N2) involvement are a heterogeneous group [18–21]. This heterogeneity involves factors such as preoperative detection, susceptibility to neoadjuvant treatment, clinically unsuspected N2 disease, and level/site and number, or both, of involved mediastinal lymph nodes [1, 22, 23].

Therefore, stage IIIA/N2 is characterized by several subgroups with variable survival rates. For example level 5, 6 N2 nodes have better prognosis, cN2 worse than respective unsuspected pN2, single versus multiple N2 stations, the number of involved lymph nodes, the extracapsular spread, the presence of subcarinal node metastasis, skip metastasis, and so forth [24, 25]. Each of these subclassifications should be considered as a completely different subpopulation of positive mediastinal lymph nodes, and highly selected patients with N2 disease achieve better 5-year results in this group [13–15]. The patterns of mediastinal lymph node metastasis reported in other reports are relatively similar to our results [2–4, 6, 26].

In our study, skip metastasis, regional spread, and one-station metastasis to mediastinal lymph nodes disclosed a clear advantage in survival rates. However, multivariate analysis established mediastinal lymph node spread at one station as the only independent favorable prognostic factor. One station favorable results are in agreement with previous reports [27–32]. Although skip metastasis and regional spread are considered significantly favorable factors in the current literature, our study reliably proves that only one-station metastasis has a positive impact on 3-year survival and nothing else. The latter challenges the results of previous studies.

One-station involvement cases did not include more cases of skip metastasis (15.5%) or cases of nonregional spread (20%) in comparison to overall incidence of these favorable factors. Thus, this particular pattern of mediastinal spread may be considered as a condition with the lower possibility for systematic extension of the malignancy. One-station metastasis should be evaluated as a solitary intrathoracic metastasis with good prognosis if it is removed along with the primary tumor.

Extraregional spread was significant as in other studies [33]. Therefore, we challenge the recommendation of a more targeted approach based on, at least partly, the lobar location of the primary tumor or with sentinel node. Complete nodal dissection or meticulous sampling of all stations in the mediastinal stations is imperative, even though for tumors small in size.

Limitations of the present study include the retrospective nature of the analysis and that the total number of nodes removed at the time of surgery is not available. Further prospective studies should be conducted using immunohistochemical node examination to detect micrometastases and to define the exact incidence of one-station N2 disease. Finally, in a future revision of the current TNM system, N2 disease should be classified into more subgroups.

In conclusion, the presence of one-station mediastinal lymph node metastasis in patients with NSCLC, who underwent major lung resection with complete mediastinal lymph node dissection, proved to be a good prognostic factor that should be taken into account in the future. This means that, to accurately determine the patient's N status, the largest possible number of the mediastinal lymph nodes should be available to the pathologist.


    References
 Top
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 References
 

  1. Hata E, Hayakawa K, Miyamoto H, Hayashida R. Rationale for extended lymphadenectomy for lung cancer Theor Surg 1990;5:19-25.
  2. Watanabe Y, Shimizu J, Tsubota M, Iwa T. Mediastinal spread of metastatic lymph nodes in bronchogenic carcinoma Chest 1990;97:1059-1065.[Medline]
  3. Libshitz HI, Mckenna RJ, Mountain CF. Patterns of mediastinal metastases in bronchogenic carcinoma Chest 1986;90:229-232.[Medline]
  4. Nohl HC. The spread of carcinoma of the bronchusLondon: Lloyd-Luke; 1962. pp. 17-44.
  5. Cerfolio RJ, Bryant AS. Distribution and likelihood of lymph node metastasis based on the lobar location of non-small cell lung cancer Ann Thorac Surg 2006;81:1969-1973.[Abstract/Free Full Text]
  6. Kotoulas CS, Foroulis CN, Kostikas K, et al. Involvement of lymphatic metastatic spread in non-small cell lung cancer accordingly to the primary cancer location Lung Cancer 2004;44:183-191.[Medline]
  7. Mountain CF. Revision of the international system for staging lung cancer Chest 1997;111:1710-1717.[Medline]
  8. Mountain CF, Dresler CM. Regional lymph node classification for lung cancer staging Chest 1997;111:1718-1723.[Medline]
  9. Takizawa T, Terashima M, Koike T, Akamatsu H, Kurita Y, Yokoyama A. Mediastinal lymph node metastasis in patients with clinical stage I peripheral non-small cell lung cancer J Thorac Cardiovasc Surg 1997;113:248-252.[Abstract/Free Full Text]
  10. Inoue M, Sawabata N, Takeda S, et al. Results of surgical intervention for p-stage III(N2) non-small cell lung cancer: acceptable prognosis predicted by complete resection in patients with single N2 disease with primary tumor in upper lobe J Thorac Cardiovasc Surg 2004;127:1100-1106.[Abstract/Free Full Text]
  11. Riquet M, Hidden G, Debesse B. Direct lymphatic drainage of lung segments to the mediastinal nodes J Thorac Cardiovasc Surg 1989;97:623-632.[Abstract]
  12. Yoshino I, Yokohama H, Yano T, et al. Skip metastasis to the mediastinal lymph nodes in non-small cell lung cancer Ann Thorac Surg 1996;62:1021-1025.[Abstract/Free Full Text]
  13. Pearson FG, De Larue NC, Ilves R, Todd TR, Cooper JD. Significance of positive superior mediastinal nodes identified at mediastinoscopy in patients with resectable cancer of the lung J Thorac Cardiovasc Surg 1982;83:1-11.[Medline]
  14. Naruke T, Goya T, Tsuchiya R, Suemasu K. The importance of surgery to non-small cell carcinoma of lung with mediastinal lymph node metastasis Ann Thorac Surg 1988;46:603-610.[Abstract]
  15. Goldstraw P, Mannam GC, Kaplan DK, Michail P. Surgical management of non-small cell lung cancer with ipsilateral mediastinal node metastasis (N2 disease) J Thorac Cardiovasc Surg 1994;107:19-28.[Abstract/Free Full Text]
  16. Roth JA, Fossella F, Komaki R, et al. A randomized trial comparing perioperative chemotherapy and surgery with surgery alone in resectable stage IIIA non-small-cell lung cancer J Natl Cancer Inst 1994;86:673-680.[Abstract/Free Full Text]
  17. Rossell R, Gomez-Codina J, Camps C, et al. A randomized trial comparing preoperative chemotherapy plus surgery with surgery alone in patients with non-small cell lung cancer N Engl J Med 1994;330:153-158.[Abstract/Free Full Text]
  18. Daly BD, Mueller JD, Faling LJ, et al. N2 lung cancer: outcome in patients with false negative computed tomographic scans of the chest J Thorac Cardiovasc Surg 1993;105904–1.
  19. Cybulsky IJ, Lanza LA, Ryan MB, et al. Prognostic significance of computed tomography in resected N2 lung cancer Ann Thorac Surg 1992;54:533-537.[Abstract]
  20. Vansteenkiste JF, De Leyn PR, Deneffe GJ, et al. Survival and prognostic factors in resected N2 non-small cell lung cancer: a study of 140 cases. Leuven Lung Cancer Group. Ann Thorac Surg 1997;63:1441-1450.[Abstract/Free Full Text]
  21. Nakanishi R, Osaki T, Nakanishi K, et al. Treatment strategy for patients with surgically discovered N2 stage IIIA nonsmall-cell lung cancer Ann Thorac Surg 1997;64:342-348.[Abstract/Free Full Text]
  22. Andre F, Grunenwald D, Pignon JP, Dujon A, Pujol JL, Brichon PY. Survival of patients with resected N2 non-small cell lung cancer: evidence of subclassification and implications J Clin Oncol 2000;18:2981-2989.[Abstract/Free Full Text]
  23. Suzuki K, Nagai K, Yoshida J, Nishimura M, Takahashi K, Nishiwaki Y. The prognosis of surgically resected N2 non-small cell lung cancer: the importance of clinical N status J Thorac Cardiovasc Surg 1999;118:145-153.[Abstract/Free Full Text]
  24. Misthos P, Sepsas E, Athanassiadi K, Kakaris S, Skottis I. Skip metastases: analysis of their clinical significance and prognosis in the IIIA/N2 NSCLC group Eur J Cardiothorac Surg 2004;25:502-508.[Abstract/Free Full Text]
  25. Detterbeck F. What to do with "surprise" N2?. Intraoperative management of patients with non-small cell lung cancer. J Thorac Oncol 2008;3:289-302.[Medline]
  26. Yoshimasu T, Miyoshi S, Oura S, Hirai I, Kokawa Y, Okamura Y. Limited mediastinal lymph node dissection for non–small cell lung cancer according to intraoperative histologic examinations J Thorac Cardiovasc Surg 2005;130:433-437.[Abstract/Free Full Text]
  27. Sakao Y, Miyamoto H, Oh S, Takahashi N, Sakuraba M. Clinicopathological factors associated with unexpected N3 in patients with mediastinal lymph node involvement J Thorac Oncol 2007;2:1107-1111.[Medline]
  28. Gawrychowski J, Gabriel A, Lackowska B. Heterogeneity of stage IIIA non-small cell lung cancers (NSCLC) and evaluation of late results of surgical treatment Eur J Surg Oncol 2003;29:178-184.[Medline]
  29. Martini N, Fleshinger BJ. The role of surgery in N2 lung cancer Surg Clin North Am 1987;67:1037-1049.[Medline]
  30. Regnard JF, Magdeleinat P, Azoulay D, et al. Results of resection for bronchogenic carcinoma with mediastinal lymph node metastases in selected patients Eur J Cardiothorac Surg 1991;5:583-587.[Abstract]
  31. Watanabe Y, Shimizu J, Oda M, et al. Aggressive surgical intervention in N2 nonsmall-cell cancer of the lung Ann Thorac Surg 1991;51:253-261.[Abstract]
  32. Sagawa M, Sakurada A, Fujimura S, et al. Five-year survivals with resected pN2 non-small cell lung carcinoma Cancer 1999;85:864-868.[Medline]
  33. Watanabe S, Suzuki K, Asamura H. Superior and basal segment lung cancers in the lower lobe have different lymph node metastatic pathways and prognosis Ann Thorac Surg 2008;85:1026-1031.[Abstract/Free Full Text]

Related Article

Invited Commentary
Frank Detterbeck
Ann. Thorac. Surg. 2008 86: 1631. [Extract] [Full Text] [PDF]



This article has been cited by other articles:


Home page
Ann. Thorac. Surg.Home page
F. Detterbeck
Invited Commentary
Ann. Thorac. Surg., November 1, 2008; 86(5): 1631 - 1631.
[Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
Panagiotis Misthos
Evangelos Sepsas
John Kokotsakis
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Misthos, P.
Right arrow Articles by Lioulias, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Misthos, P.
Right arrow Articles by Lioulias, A.
Related Collections
Right arrow Lung - cancer
Right arrowRelated Article


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ANN THORAC SURG ASIAN CARDIOVASC THORAC ANN EUR J CARDIOTHORAC SURG
J THORAC CARDIOVASC SURG ICVTS ALL CTSNet JOURNALS