Controversies of the optimal surgical management for the lymph nodes in non-small cell lung cancer
Editorial

Controversies of the optimal surgical management for the lymph nodes in non-small cell lung cancer

Aritoshi Hattori, Kenji Suzuki

Department of General Thoracic Surgery, Juntendo University School of Medicine, Tokyo, Japan

Correspondence to: Kenji Suzuki, MD. Department of General Thoracic Surgery, Juntendo University School of Medicine, 1-3, Hongo 3-chome, Bunkyo-ku, Tokyo, 113-8431, Japan. Email: kjsuzuki@juntendo.ac.jp.

Comment on: Liang W, He J, Shen Y, et al. Impact of Examined Lymph Node Count on Precise Staging and Long-Term Survival of Resected Non-Small-Cell Lung Cancer: A Population Study of the US SEER Database and a Chinese Multi-Institutional Registry. J Clin Oncol 2017;35:1162-70.


Received: 28 August 2017; Accepted: 15 September 2017; Published: 18 September 2017.

doi: 10.21037/shc.2017.09.02


Lobectomy with lymph nodal dissection is currently the standard surgical strategy for resectable non-small cell lung cancer (NSCLC). This is largely dependent on the only randomized prospective trial comparing lobectomy with sublobar resections reported by Lung Cancer Study Group in 1995 (1). With regard to the appropriate lymph nodal dissection for surgically resected NSCLC, complete hilar and mediastinal lymphadenectomy, i.e., radical systematic mediastinal lymph nodal dissection, is widely recognized as an essential local management strategy ever since reported by Cahan in 1960 (2). In general, complete hilar and mediastinal lymphadenectomy requires “en bloc” resection of the lymph nodes based on the established anatomical boundaries. It is considered that patients with positive lymph nodal metastases could have a potential risk for the locoregional and/or distant recurrence of lung cancer. Hence, complete lymphadenectomy for NSCLCs plays a pivotal role in that it provides the most reliable information regarding cancer staging and prognosis. In addition, radical lymphadenectomy could reduce the risk of undetected positive lymph nodes which may result in a thorough retrieve of the remnants, and proper delivery of optimal postoperative treatment which may contribute to the survival outcomes (3,4). However, it is still controversial with regard to the actual oncological benefit which the radical lymphadenectomy would provide for.

In this context, how to remove the lymph nodes properly in patients with resectable NSCLC have been widely discussed in the general thoracic surgical community. Several controversies exist with regard to the optimal surgical management of the lymph node for resectable NSCLC. The first is about the concept to decide how to harvest the lymph nodes. Recently, some randomized controlled trials that compared systematic lymph nodal dissection with systematic lymph nodal sampling have been performed (5,6). Although these prospective trials have not demonstrated the definitive survival benefit of systematic lymph node dissection, the current guidelines still recommends systematic lymph nodal dissection for all resectable NSCLC despite the tumor stage or location of the tumor from the point of preventing locoregional recurrence as much as possible after lung cancer surgery (7,8). The second is about the extent of lymph node dissection. Several institutional retrospective studies have recently demonstrated detailed nodal spread patterns in surgically resected early-stage NSCLC (9,10), and lobe-specific lymph nodal dissection has been widely recognized on the basis of these results. Furthermore, previous retrospective studies have suggested that survival and recurrence may be identical between systematic and lobe-specific lymph nodal dissection in early-stage NSCLC (11-13). To elucidate the survival benefit or inferiority regarding the extent of lymph nodal dissection, further study is needed and prospective clinical trial has been conducted for radiologic invasive NSCLC in Japan.

And the third controversy, the topic on this issue, is about a prognostic importance of the number of resected lymph node or positive lymph node number/ratio in patients with NSCLC (14). It is considered that the greater number of examined lymph nodes can reduce the risk of undetected positive lymph nodes, which may contribute to the accurate tumor staging and definite retrieve of remnants, and subsequent administration of adjuvant chemotherapy to improve survival outcomes. Generally, the number of examined lymph nodes is considered to be a significantly associated with improved survival as shown in breast or several gastrointestinal cancers. Unlike other organ cancers, however, distribution of the lymph nodes is recognized as “station” surrounded by anatomical boundaries in patients with NSCLC based on the IASLC staging rule (15). Hence, the concept of optimal lymph node count prevailed in several organ cancers may somewhat different from that of lung cancer to date. However, the topic on this issue may provide new information for determining the refined N category in the future TNM classification of lung cancer.

In the issue of the Journal of Clinical Oncology (JCO), Liang and colleagues analyzed the impact of examined lymph node count on precise staging and long-term survival of resected NSCLC using the currently largest data sets from a Chinese multi-institutional registry and the US SEER database on stage I to IIIA resected NSCLC (14). They concluded that a greater number of examined lymph nodes are associated with more accurate node staging and better long-term survival of resected NSCLC. Furthermore, the paper recommended to retrieve at least 16 or more lymph nodes for evaluating the quality of nodal examination or proper stratification postoperatively not only for patients with node positive patient but node negative one. So far, recommendation on the examined lymph node count have not been made in the NCCN guidelines for lung cancer (7), but several retrospective studies have attempted to determine a benchmark of the resected lymph node count (14,16,17). Furthermore, the TNM rules suggest that at least six lymph nodes need to be removed, three from N1 and three from N2 stations. This is the minimum requirement for a diagnosis of N0 when lymph nodes are negative (18). Rigorous examination of the lymph node by the thoracic surgeons would results in more accurate cancer staging and possible survival benefit due to the detection and retrieve of the involved lymph node in patients with NSCLC. Hence, study as for the prognostic importance of examined lymph nodal count will be a new challenge in the thoracic oncology to establish the accurate stage of lung cancer patient, administrate the optimal therapeutic modality and improve the prognosis.

In the field of lung cancer surgery, however, previous analyses on this topic have found somewhat contradictory results (14,16,17,19,20). Several problems exist that should be resolved to discuss this important topic. First, the number of resected lymph nodes would be highly variable from one patient to another, which is relied on the malignant potential of the main tumor and the expected clinical N status (19). Also, extent of the lymph node resection or examined lymph node count would be highly affected by the patient comorbid status (21).

Second, the method used to evaluate harvested lymph nodes needs to be standardized. Usually, when systematic lymph node dissection is performed, the lymph nodes should be dissected en bloc together with surrounding adipose tissue as a lump (15). Ideally, pathologists or surgeons should remove these nodes out as distinct nodes, not as fragments. Otherwise, some of the nodes can be missed without undergoing a pathological assessment (20). It is also reported that missed intrapulmonary lymph node metastasis affect the nodal staging quality gap, which contribute to the poor prognosis (20). More rigorous gross dissection of the resected lung cancer specimens may provide prognostically useful information.

Third, as noted by Liang and colleague, it is interesting to investigate the correlation between the examined lymph node count and the N1/N2 stations based on the 8th N staging. The 8th TNM staging suggests that the combination of location of metastatic nodes, number of involved node (single station versus multiple stations), and absence versus presence of skip metastasis as pN0, pN1a, pN1b, pN2a1, pN2a2, and pN2b may give a more accurate prognosis (15). These classifications require prospective evaluation before being considered for future revisions of the TNM staging system for lung cancer.

The fourth is about the problem of the potential risk in this study; overestimation of unsatisfactory harvesting in patients with a greater number of lymph nodes and underestimation of satisfied lymphadenectomy in patients with a smaller number of resected lymph node (19). This may be a potential bias in this study. To date, systematic lymphadenectomy is accepted as a principle procedure in lung cancer surgery, because the lymph node location can be easily determined on computed tomography (CT) or positron emission tomography (PET). Categorization based on the “station” used in the IASLC staging system is anatomically reasonable from the perspective of a lymphatic pathway from the lung parenchyma through the hilum, mediastinum, and supraclavicular fossa (15). Therefore, in the future, it is necessary to uniform the lymph node counting method to adopt the concept as a new N descriptor.

Finally, we should consider the expected frequencies of pathological nodal involvement in patients with clinically node negative one based on the radiological findings of the main tumor, which would greatly contribute to the appropriate surgical resection of the lymph node. Because of the refined resolution of thin-section CT scan or the advent of the 18F-fluorodeoxyglucose PET, small-sized or early-stage lung cancer have been detected frequently. Based on the studies of radiological and pathological correlation of lung cancer in Japan (22), we can predict tumor invasiveness and probability of lymph nodal metastasis more precisely on the basis of the preoperative radiologic characteristics. Among them, the presence of a ground-grass opacity (GGO) component, which would represent adenocarcinoma of the lung almost for all, is considered to denote a good prognosis, and in most cases the pathologic features are minimally invasive because of a significant correlation with histologic lepidic growths (23,24). The estimated rate of lymph node metastasis in part-solid lung adenocarcinoma is considered to be about 5% (23,24). Recent studies demonstrated that GGO-dominant tumors are truly localized disease and their pathological features are likely to be indolent, which would be enough with lobe-specific nodal dissection, or may not require nodal dissection in selected cases (11,12). Traditionally, however, a radiologic pure-solid lung adenocarcinoma without any GGO component is assumed to show a highly malignant nature, and postoperative nodal involvement is found in approximately 15% to 20% of clinically node negative cases, even in those with small-sized lesions (23-25). This may be a detection limit in the present day. Therefore, accurate decision for the extent of lymph nodal dissection/resection would be needed in accordance with the tumor invasiveness in reference to the findings on thin-section CT scan or FDG-PET in the future.

At all events, the impact of examined lymph node count on the prognosis would be an important theme that should be addressed intensively in general thoracic surgery. It is still controversial with regard to the prognostic significance of lymph nodal dissection, however, what we have to perform is definite local control by the strict nodal resection. The diagnosis of malignant potential for lung cancers has been refined based on the numerous studies to evaluate the radiological and pathological correlation in thoracic oncology. According to this, further research will be needed to confirm the prognostic impact of lymph nodal resection, considering the several concepts regarding nodal management in patients with NSCLC, such as optimal method to harvest of lymph node, appropriate extent of lymph node, involved lymph node ratio, and importance of examined lymph node count.


Acknowledgments

Funding: None.


Footnote

Provenance and Peer Review: This article was commissioned by the editorial office, Shanghai Chest. The article did not undergo external peer review.

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/shc.2017.09.02). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


References

  1. Ginsberg RJ, Rubinstein LV. Randomized trial of lobectomy versus limited resection for T1 N0 non-small cell lung cancer. Lung Cancer Study Group. Ann Thorac Surg 1995;60:615-22; discussion 622-3. [Crossref] [PubMed]
  2. Cahan WG. Radical lobectomy. J Thorac Cardiovasc Surg 1960;39:555-72. [PubMed]
  3. Arriagada R, Bergman B, Dunant A, et al. Cisplatin-based adjuvant chemotherapy in patients with completely resected non-small-cell lung cancer. N Engl J Med 2004;350:351-60. [Crossref] [PubMed]
  4. Winton T, Livingston R, Johnson D, et al. Vinorelbine plus cisplatin vs. observation in resected non-small-cell lung cancer. N Engl J Med 2005;352:2589-97. [Crossref] [PubMed]
  5. Darling GE, Allen MS, Decker PA, et al. Randomized trial of mediastinal lymph node sampling versus complete lymphadenectomy during pulmonary resection in the patient with N0 or N1 (less than hilar) non-small cell carcinoma: results of the American College of Surgery Oncology Group Z0030 Trial. J Thorac Cardiovasc Surg 2011;141:662-70. [Crossref] [PubMed]
  6. Izbicki JR, Passlick B, Pantel K, et al. Effectiveness of radical systematic mediastinal lymphadenectomy in patients with resectable non-small cell lung cancer: results of a prospective randomized trial. Ann Surg 1998;227:138-44. [Crossref] [PubMed]
  7. National Comprehensive Cancer Network. Non-small cell lung cancer (version 3. 2014). Available online: http://www.nccn.org/professionals/physician_gls/pdf/nscl.pdf
  8. Lardinois D, De Leyn P, Van Schil P, et al. ESTS guidelines for intraoperative lymph node staging in non-small cell lung cancer. Eur J Cardiothorac Surg 2006;30:787-92. [Crossref] [PubMed]
  9. Asamura H, Nakayama H, Kondo H, et al. Lobe-specific extent of systematic lymph node dissection for non-small cell lung carcinomas according to a retrospective study of metastasis and prognosis. J Thorac Cardiovasc Surg 1999;117:1102-11. [Crossref] [PubMed]
  10. Okada M, Tsubota N, Yoshimura M, et al. Proposal for reasonable mediastinal lymphadenectomy in bronchogenic carcinomas: role of subcarinal nodes in selective dissection. J Thorac Cardiovasc Surg 1998;116:949-53. [Crossref] [PubMed]
  11. Haruki T, Aokage K, Miyoshi T, et al. Mediastinal nodal involvement in patients with clinical stage I non-small-cell lung cancer: possibility of rational lymph node dissection. J Thorac Oncol 2015;10:930-6. [Crossref] [PubMed]
  12. Hishida T, Miyaoka E, Yokoi K, et al. Lobe-Specific Nodal Dissection for Clinical Stage I and II NSCLC: Japanese Multi-Institutional Retrospective Study Using a Propensity Score Analysis. J Thorac Oncol 2016;11:1529-37. [Crossref] [PubMed]
  13. Okada M, Sakamoto T, Yuki T, et al. Selective mediastinal lymphadenectomy for clinico-surgical stage I non-small cell lung cancer. Ann Thorac Surg 2006;81:1028-32. [Crossref] [PubMed]
  14. Liang W, He J, Shen Y, et al. Impact of Examined Lymph Node Count on Precise Staging and Long-Term Survival of Resected Non-Small-Cell Lung Cancer: A Population Study of the US SEER Database and a Chinese Multi-Institutional Registry. J Clin Oncol 2017;35:1162-70. [Crossref] [PubMed]
  15. Asamura H, Chansky K, Crowley J, et al. The International Association for the Study of Lung Cancer Lung Cancer Staging Project: Proposals for the Revision of the N Descriptors in the Forthcoming 8th Edition of the TNM Classification for Lung Cancer. J Thorac Oncol 2015;10:1675-84.
  16. David EA, Cooke DT, Chen Y, et al. Does Lymph Node Count Influence Survival in Surgically Resected Non-Small Cell Lung Cancer? Ann Thorac Surg 2017;103:226-35. [Crossref] [PubMed]
  17. Saji H, Tsuboi M, Yoshida K, et al. Prognostic impact of number of resected and involved lymph nodes at complete resection on survival in non-small cell lung cancer. J Thorac Oncol 2011;6:1865-71. [Crossref] [PubMed]
  18. UICC International Union Against Cancer. TNM Classification of Malignant Tumours. 7th edition. New York: Wiley-Blackwell, 2009.
  19. Riquet M, Legras A, Mordant P, et al. Number of mediastinal lymph nodes in non-small cell lung cancer: a Gaussian curve, not a prognostic factor. Ann Thorac Surg 2014;98:224-31. [Crossref] [PubMed]
  20. Smeltzer MP, Faris N, Yu X, et al. Missed Intrapulmonary Lymph Node Metastasis and Survival After Resection of Non-Small Cell Lung Cancer. Ann Thorac Surg 2016;102:448-53. [Crossref] [PubMed]
  21. Altorki NK, Kamel MK, Narula N, et al. Anatomical Segmentectomy and Wedge Resections Are Associated with Comparable Outcomes for Patients with Small cT1N0 Non-Small Cell Lung Cancer. J Thorac Oncol 2016;11:1984-92. [Crossref] [PubMed]
  22. Suzuki K, Koike T, Asakawa T, et al. A prospective radiological study of thin-section computed tomography to predict pathological noninvasiveness in peripheral clinical IA lung cancer (Japan Clinical Oncology Group 0201). J Thorac Oncol 2011;6:751-6. [Crossref] [PubMed]
  23. Hattori A, Matsunaga T, Takamochi K, et al. Neither Maximum Tumor Size nor Solid Component Size Is Prognostic in Part-Solid Lung Cancer: Impact of Tumor Size Should Be Applied Exclusively to Solid Lung Cancer. Ann Thorac Surg 2016;102:407-15. [Crossref] [PubMed]
  24. Hattori A, Matsunaga T, Takamochi K, et al. Importance of Ground Glass Opacity Component in Clinical Stage IA Radiologic Invasive Lung Cancer. Ann Thorac Surg 2017;104:313-20. [Crossref] [PubMed]
  25. Hattori A, Matsunaga T, Hayashi T, et al. Prognostic Impact of the Findings on Thin-Section Computed Tomography in Patients with Subcentimeter Non-Small Cell Lung Cancer. J Thorac Oncol 2017;12:954-62. [Crossref] [PubMed]
doi: 10.21037/shc.2017.09.02
Cite this article as: Hattori A, Suzuki K. Controversies of the optimal surgical management for the lymph nodes in non-small cell lung cancer. Shanghai Chest 2017;1:38.

Download Citation