Skip to main content

Advertisement

Log in

Is tumor diameter a risk factor for occult N1 metastasis in patients with peripheral non-small cell lung cancer which is smaller than 3 cm?

  • Original Article
  • Published:
Updates in Surgery Aims and scope Submit manuscript

Abstract

The optimum treatment option is surgery for clinical early stage non-small cell lung cancer. Despite all non-invasive and invasive staging effort, occult lymph-node metastasis can be detected in pathological staging. Here, we investigated whether there was any correlation between tumor diameter and occult lymph-node metastasis in N1 stations. Data of patient with non-small cell lung cancer clinical stage 1A were reviewed retrospectively. Those with tumor diameter smaller than 3 cm and pN0-pN1 in pathological staging were included in the study. Overall survival (OS) was calculated by Kaplan–Meier and survival differences between pN0 and pN1 groups were investigated by Log-Rank methods. Cut-off value of tumor diameter for lymph-node metastasis was investigated by Receiver-Operating Characteristics test. Significance between pN0-pN1 and other categorical groups was investigated with Pearson Chi-square or Fisher’s exact tests. A total of 257 patients meet to criteria included in the study. Fifty-five (21.4%) of the patients were females. The mean age was 62.7 ± 8.5 and median tumor diameter was 20 mm (Range: 2–30 mm). We detected occult lymph-node metastasis at the N1 stations (pN1) in 33 patients (12.8%) in histopathological examination of resected specimens and lymph-node dissection materials. The cut-off value of tumor diameter was calculated as 21.5 mm for occult lymph-node metastasis by Receiver-Operating Characteristics analysis (Area Under Curved: 70.1%, p = 0.004). There was a significant correlation between pN1 positivity and high tumor diameter (p = 0.02). However, we did not find a correlation between the lymph-node metastasis and age, gender, tumor histopathology, tumor localization, and visceral pleural invasion. Tumor diameter may be an indicator for occult lymph-node metastasis in patients with clinical stage-1A non-small cell lung cancer. This result should be considered in patient with mass which larger than 21.5 mm and planned stereotactic body radiotherapy instead of surgery.

Graphical abstract

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

Data availability

The data that support the findings of this study are available from the corresponding author, upon reasonable request.

References

  1. Detterbeck FC, Jantz MA, Wallace M, Vansteenkiste J, Silvestri GA (2007) American college of chest physicians. Invasive mediastinal staging of lung cancer: ACCP evidence-based clinical practice guidelines (2nd edition). Chest 132(3 Suppl):202S-220S. https://doi.org/10.1378/chest.07-1362

    Article  PubMed  Google Scholar 

  2. De Leyn P, Dooms C, Kuzdzal J, Lardinois D, Passlick B, Rami-Porta R, Turna A, Van Schil P, Venuta F, Waller D, Weder W, Zielinski M (2014) Revised ESTS guidelines for preoperative mediastinal lymph node staging for non-small-cell lung cancer. Eur J Cardiothorac Surg 45(5):787–798. https://doi.org/10.1093/ejcts/ezu028

    Article  PubMed  Google Scholar 

  3. Seok Y, Yang HC, Kim TJ, Lee KW, Kim K, Jheon S, Cho S (2014) Frequency of lymph node metastasis according to the size of tumors in resected pulmonary adenocarcinoma with a size of 30 mm or smaller. J Thorac Oncol 9(6):818–824. https://doi.org/10.1097/JTO.0000000000000169

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Lv X, Wu Z, Cao J, Hu Y, Liu K, Dai X, Yuan X, Wang Y, Zhao K, Lv W, Hu J (2021) A nomogram for predicting the risk of lymph node metastasis in T1–2 non-small-cell lung cancer based on PET/CT and clinical characteristics. Transl Lung Cancer Res 10(1):430–438. https://doi.org/10.21037/tlcr-20-1026

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Prezzano KM, Ma SJ, Hermann GM, Rivers CI, Gomez-Suescun JA, Singh AK (2019) Stereotactic body radiation therapy for non-small cell lung cancer: a review. World J Clin Oncol 10:14–27. https://doi.org/10.5306/wjco.v10.i1.14

    Article  PubMed  PubMed Central  Google Scholar 

  6. Onishi H, Shirato H, Nagata Y, Hiraoka M, Fujino M, Gomi K, Karasawa K, Hayakawa K, Niibe Y, Takai Y, Kimura T, Takeda A, Ouchi A, Hareyama M, Kokubo M, Kozuka T, Arimoto T, Hara R, Itami J, Araki T (2011) Stereotactic body radiotherapy (SBRT) for operable stage I non-small-cell lung cancer: can SBRT be comparable to surgery? Int J Radiat Oncol Biol Phys 81(5):1352–1358. https://doi.org/10.1016/j.ijrobp.2009.07.1751

    Article  PubMed  Google Scholar 

  7. Ward MC, Oh SC, Pham YD, Woody NM, Marwaha G, Videtic GM, Stephans KL (2016) Isolated nodal failure after stereotactic body radiotherapy for lung cancer: The role for salvage mediastinal radiotherapy. J Thorac Oncol 11(9):1558–1564. https://doi.org/10.1016/j.jtho.2016.05.003

    Article  PubMed  Google Scholar 

  8. Moulla Y, Gradistanac T, Wittekind C, Eichfeld U, Gockel I, Dietrich A (2019) Predictive risk factors for lymph node metastasis in patients with resected non-small cell lung cancer: a case control study. J Cardiothorac Surg 14(1):11. https://doi.org/10.1186/s13019-019-0831-0.Erratum.In:JCardiothoracSurg.2019;14(1):31

    Article  PubMed  PubMed Central  Google Scholar 

  9. Jia B, Chen B, Long H, Rong T, Su X (2020) Tumor volume is more reliable to predict nodal metastasis in non-small cell lung cancer of 30 cm or less in the greatest tumor diameter. World J Surg Oncol 18:168. https://doi.org/10.1186/s12957-020-01946-0

    Article  PubMed  PubMed Central  Google Scholar 

  10. Akthar AS, Ferguson MK, Koshy M, Vigneswaran WT, Malik R (2017) Limitations of PET/CT in the detection of occult N1 metastasis in clinical stage I(T1-2aN0) non-small cell lung cancer for staging prior to stereotactic body radiotherapy. Technol Cancer Res Treat 16:15-21. https://doi.org/10.1177/1533034615624045.

    Article  CAS  Google Scholar 

  11. Kukhon FR, Lan X, Helgeson SA, Arunthari V, Fernandez-Bussy S, Patel NM (2021) Occult lymph node metastasis in radiologic stage I non-small cell lung cancer: the role of endobronchial ultrasound. Clin Respir J 15:676–682. https://doi.org/10.1111/crj.13344

    Article  CAS  PubMed  Google Scholar 

  12. Robinson EM, Ilonen IK, Tan KS, Plodkowski AJ, Bott M, Bains MS, Adusumilli PS, Park BJ, Rusch VW, Jones DR, Huang J (2020) Prevalence of occult peribronchial N1 nodal metastasis in peripheral clinical N0 small (≤2 cm) non-small cell lung cancer. Ann Thorac Surg 109:270–276. https://doi.org/10.1016/j.athoracsur.2019.07.037

    Article  PubMed  Google Scholar 

  13. Kawamoto N, Tsutani Y, Kamigaichi A, Ohsawa M, Mimae T, Miyata Y, Okada M (2023) Tumour location predicts occult N1 nodal metastasis in clinical stage I non-small-cell lung cancer. Eur J Cardiothorac Surg 63(2):ezac575. https://doi.org/10.1093/ejcts/ezac575.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Cho JY, Leem CS, Kim Y, Kim ES, Lee SH, Lee YJ, Park JS, Cho YJ, Lee JH, Lee CT, Yoon HI (2018) Solid part size is an important predictor of nodal metastasis in lung cancer with a subsolid tumor. BMC Pulm Med 18(1):151. https://doi.org/10.1186/s12890-018-0709-2

    Article  PubMed  PubMed Central  Google Scholar 

  15. Liu J, Li J, Lin G, Long Z, Li Q, Liu B (2020) Risk factors of lobar lymph node metastases in non-primary tumor-bearing lobes among the patients of non-small-cell lung cancer. PLoS One 15(9):e0239281. https://doi.org/10.1371/journal.pone.0239281

    Article  PubMed  Google Scholar 

  16. Song CY, Kimura D, Sakai T, Tsushima T, Fukuda I (2019). Novel approach for predicting occult lymph node metastasis in peripheral clinical stage I lung adenocarcinoma. J Thorac Dis 11(4):1410-1420. https://doi.org/10.21037/jtd.2019.03.57.

    Article  PubMed  Google Scholar 

  17. Moon Y, Choi SY, Park JK, Lee KY (2020) Risk factors for occult lymph node metastasis in peripheral non-small cell lung cancer with invasive component size 3 cm or less. World J Surg 44(5):1658-1665. https://doi.org/10.1007/s00268-019-05365-5.

    Article  PubMed  Google Scholar 

  18. Kaseda K, Asakura K, Kazama A, Ozawa Y (2016) Risk factors for predicting occult lymph node metastasis in patients with clinical stage I non-small cell lung cancer staged by integrated fluorodeoxyglucose positron emission tomography/computed tomography. World J Surg 40:2976-2983. https://doi.org/10.1007/s00268-016-3652-5.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Batıhan G, Ceylan KC, Üçvet A, Kaya ŞÖ, Yazgan S (2023). Analysis of prognostic factors in pT1-2 N1 lung cancer patients in the light surgical results. Updates Surg https://doi.org/10.1007/s13304-023-01473-z.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Ito R, Tsukioka T, Izumi N, Komatsu H, Inoue H, Kimura T, Kishimoto K, Nishiyama N (2022) Lymph node metastasis location and postoperative adjuvant chemotherapy in patients with pN1 stage IIb nonsmall cell lung cancer. In Vivo 36(1):355-60. https://doi.org/10.21873/invivo.12710.

    Article  PubMed  Google Scholar 

  21. Hu F, Lin C, Chu H, Ren P, Wang J, Ma S (2021). Prognostic value of different N1 lymph node zones in pN1M0 non-small cell lung cancer: a systematic review and meta-analysis. Sci Rep 11(1):21606. https://doi.org/10.1038/s41598-021-01136-2.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

The authors would like to thank Dr. Ismail Cuneyt Kurul, MD, Professor, Head of our Department, for his endless supports for the study and revision.

Funding

Nil.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Muhammet Sayan.

Ethics declarations

Conflict of interest

Authors declare that there is no conflict of interest.

Human and animal rights

The study including human participants has been performed in accordance with the ethical standards of the Declaration of Helsinki and its later amendments.

Informed consent

For this retrospective study, informed consent is not required.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sayan, M., Celik, A., Kankoc, A. et al. Is tumor diameter a risk factor for occult N1 metastasis in patients with peripheral non-small cell lung cancer which is smaller than 3 cm?. Updates Surg 75, 2335–2342 (2023). https://doi.org/10.1007/s13304-023-01575-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13304-023-01575-8

Keywords

Navigation