Pulmonary segmentectomy for early stage non-small cell lung cancer: when, for which cases and how
Editorial

Pulmonary segmentectomy for early stage non-small cell lung cancer: when, for which cases and how

Natsumi Matsuura, Toshiki Yajima

Department of General Thoracic, Breast and Endocrinological Surgery, Kagawa University, Kagawa, Japan

Correspondence to: Natsumi Matsuura, MD, PhD. 1750-1 Ikenobe, Miki-cho, Kita-Gun, Kagawa 761-0793, Japan. Email: nmori1130@gmail.com.

Comment on: Wang G, Yu Z, Li J, et al. Anatomical segmentectomy under uniportal video-assisted thoracoscopic surgery for early staged non-small cell lung cancer: a case report. J Thorac Dis 2022;14:3613-23.


Keywords: Lung cancer; early stage lung cancer; segmentectomy


Submitted Jan 13, 2023. Accepted for publication Feb 03, 2023. Published online Feb 20, 2023.

doi: 10.21037/jtd-23-66


Times have changed since lobectomy was considered a curative surgery for lung cancer (1), and segmentectomy is now beginning to be recognized as an alternative surgical procedure for early stage lung cancer. Detailed qualitative diagnosis with thin section helical computed tomography (CT) and improved imaging techniques, such as positron emission tomography (PET), have made it possible to detect smaller lung cancers and at an earlier stage. Attempts at limited surgery and preservation of pulmonary function for these lung cancers are a natural progression. Segmentectomy has been reported to be equivalent in radicality and less invasive compared with lobectomy (2-4). Moreover, the results of a Japanese randomized controlled trial comparing lobectomy with segmentectomy for patients with clinical stage IA non-small cell lung cancer (NSCLC) [tumor diameter ≤2 cm; consolidation-to-tumor (C/T) ratio >0.5] (JCOG0802/WJOG4607L) showed the benefits of segmentectomy versus lobectomy in terms of overall survival (5). Although the indications for segmentectomy are expected to expand, there are still differences between institutions regarding the indications for segmentectomy, including ground-glass opacity (GGO) dominant lesions, and the detailed surgical modalities (intersegmental identification and dissection methods, with or without lymph node dissection, etc.). Wang et al. reported the right apical segmentectomy under uniportal video-assisted thoracoscopic surgery for bilateral synchronous pure GGO lesions, and also raised some important questions about segmentectomy for early stage lung cancer (6), including when, for which cases and how to perform a segmentectomy.

With improvements in imaging technology, thin-section CT is now commonly available, and several attempts to identify early stage lung cancer with less invasiveness have been reported. The JCOG0201 trial investigated the association between pathological invasiveness and radiological findings in patients with clinical T1N0M0 peripheral (in the outer half of the lung field) lung cancer to determine the indications for limited surgery, and revealed that pathologically non-invasive cancer can be predicted by a cut-off value of a C/T ratio of 0.25 with a specificity of 98.7% [95% confidence interval (CI): 93.2–100.0%] for lung cancer ≤2.0 cm in size (7). Based on these results, a trial was conducted to evaluate the efficacy and safety of sublobar resection for GGO dominant peripheral lung cancers with ≤2.0 cm in size and with a C/T ratio ≤0.25 (JCOG0804/WJOG4507L trial) (8). In this trial, intraoperative confirmation of a macroscopic surgical margin of ≥5 mm and the histology of the primary tumor by frozen-section were mandatory, and conversion to segmentectomy or lobectomy from wedge resection was at the surgeon’s discretion. Wedge resection was performed in 79.3% of the cases, resulting in a 5-year relapse free rate of 99.7% (90% CI: 98.3–99.9%), with no local relapse. These results suggest that wedge resection might be sufficient when the radiologically non-invasive lung cancer is located in the outer third of the lung field, while a segmentectomy is required when sufficient margins are not secured.

There is also the question of when to operate on radiologically non-invasive tumors. Multiple GGO lesions in multiple different lobes on both sides, as in the case presented by Wang et al. (6), are frequently experienced and are commonly resected from tumors of larger diameter or those with a solid component. In a multicenter study that observed the natural history of pulmonary subsolid nodules, the frequency of pure GGO lesions developing into part-solid nodules during a 5-year follow-up period was low, at 5.6%, although 24% of part-solid GGO tumors with a solid component of 3 mm or less at the time of first detection showed a trend towards increase in the solid component at 2.4±1.3 years (9). This suggest that pure GGO and part-solid GGO tumors differ in terms of the optimal surgical timing and surgical procedure. A follow-up observation study is currently underway in Japan for radiologically non-invasive tumors with a maximum tumor diameter of ≤2 cm and C/T ratio of ≤0.25 on thin-section CT (JCOG1906 trial), and the results of this trial will be an important indicator in the future regarding optimal surgical timing. Actually, the indications and the surgical procedure are likely to be determined by taking into account the location of the tumor and radiologic findings, as well as the patient’s age, request, and cardiopulmonary function in general.

Another important issue is the extent of lymph node dissection. Katsumata et al. compared the result of preoperative CT imaging with the pathological results in completely resected early stage lung cancer, and reported that lung cancer that is clinically T1a or less or with a C/T ratio of 0.5 or less is usually pathologically noni-invasive, with no nodal involvement and no vessel invasion (10). Zhang et al. analyzed the data on 2,749 patients with invasive NSCLC who underwent pulmonary resection with systemic lymph node dissection, and reported that tumors with a C/T ratio of ≤0.5 had no lymph node involvement (11). In the aforementioned JCOG0804/WJOG4507L trial (8), lymph node dissection was not mandatory for hilar and mediastinal nodes, and in more than 70% of cases no lymph nodes were removed. Based on these results, it can be said that lymph node dissection is not necessary for radiologically non-invasive tumors (≤2.0 cm in size and C/T ratio of ≤0.25). However, for tumors with C/T ratio >0.5 covered by the JCOG0802/WJOG4607L trial, intraoperative confirmation of the absence of metastases in the hilar lymph nodes is essential. If metastases are found in the hilar lymph nodes, a change of surgical procedure should be considered. The results of trials of segmentectomy for tumors with C/T ratio >0.25 to ≤0.5 are currently awaited (JCOG1211 trial).

Now that thoracoscopic surgery is more common, it is important to ensure an adequate surgical margin in addition to the correct intersegmental dissection when performing segmentectomy for lesions that cannot be palpated intraoperatively. As far as limited surgery is concerned, preventing local recurrence is of paramount importance. Various methods for intersegmental identification have been reported (12-16), such as intravenous indocyanine green (ICG) injection and near infrared thoracoscopy, which are now widely used to identify the intersegmental plane (12,13,17). Intravenous ICG administration is simple and rapid, and identification with ICG does not require the lung to be inflated and does not obstruct the surgeon’s view during thoracoscopic surgery. The ICG method identifies the intersegmental planes along the course of blood flow, but methods for identifying the planes along the airways, such as inflation-deflation and jet ventilation, are also commonly used, and a combination of both might be even more useful. Moreover, it has been reported that more than one-third of p-T1N0M0 NSCLCs extend beyond one segment regardless of size (18), suggesting that attempts should be made to resect two segments or combine subsegmentectomy to ensure sufficient margins.

Currently, there is a transition in surgical approaches from thoracotomy to multiportal video-assisted thoracoscopic surgery (VATS), with further uniportal and robot-assisted thoracoscopic surgery (RATS). Uniportal VATS segmentectomy is now widely performed and satisfactory perioperative results have been reported (19-21). Uniportal VATS requires unique surgical techniques, and Wang et al. described the surgical procedure for uniportal thoracoscopic segmentectomy in detail, with excellent results (6). Whatever the approach, it is important that surgical margins around the tumor are ensured, correct intersegmental (and sometimes subsegmental) dissection is achieved, and residual lung function is preserved as much as possible by preserving the intersegmental veins. With regard to lung function, there is still room for debate on the effect of segmentectomy on preservation of lung function. In a randomized controlled trial confirming the noninferiority of segmentectomy to lobectomy (JCOG0802/WJOG4607L) (5), the median reduction in forced expiratory volume in 1 second (FEV1) at 1 year postoperatively was 12.0% in the segmentectomy group and 8.5% in the lobectomy group (between-group difference: 3.5%, P<0.0001), although the difference did not reach the predefined threshold for clinical significance of 10% at 1-year follow-up. However, various factors that cannot be determined by lung function data alone might also contribute to long-term survival, such as improved subjective symptoms due to less residual lung and mediastinal excursion, better general condition, and easier access to treatment for a second cancer. The relationship between preservation of lung parenchyma and long-term survival will require further investigation.


Acknowledgments

Funding: None.


Footnote

Provenance and Peer Review: This article was commissioned by the editorial office, Journal of Thoracic Disease. This article did not undergo external peer review.

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at https://jtd.amegroups.com/article/view/10.21037/jtd-23-66/coif). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work and 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;60:615-23. [Crossref] [PubMed]
  2. Okada M, Koike T, Higashiyama M, et al. Radical sublobar resection for small-sized non-small cell lung cancer: a multicenter study. J Thorac Cardiovasc Surg 2006;132:769-75. [Crossref] [PubMed]
  3. Tosi D, Nosotti M, Bonitta G, et al. Anatomical segmentectomy versus pulmonary lobectomy for stage I non-small-cell lung cancer: patients selection and outcomes from the European Society of Thoracic Surgeons database analysis. Interact Cardiovasc Thorac Surg 2021;32:546-51. [Crossref] [PubMed]
  4. Nomori H, Yamazaki I, Machida Y, et al. Lobectomy versus segmentectomy: a propensity score-matched comparison of postoperative complications, pulmonary function and prognosis. Interact Cardiovasc Thorac Surg 2022;34:57-65. [Crossref] [PubMed]
  5. Saji H, Okada M, Tsuboi M, et al. Segmentectomy versus lobectomy in small-sized peripheral non-small-cell lung cancer (JCOG0802/WJOG4607L): a multicentre, open-label, phase 3, randomised, controlled, non-inferiority trial. Lancet 2022;399:1607-17. [Crossref] [PubMed]
  6. Wang G, Yu Z, Li J, et al. Anatomical segmentectomy under uniportal video-assisted thoracoscopic surgery for early staged non-small cell lung cancer: a case report. J Thorac Dis 2022;14:3613-23. [Crossref] [PubMed]
  7. 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]
  8. Suzuki K, Watanabe SI, Wakabayashi M, et al. A single-arm study of sublobar resection for ground-glass opacity dominant peripheral lung cancer. J Thorac Cardiovasc Surg 2022;163:289-301.e2. [Crossref] [PubMed]
  9. Kakinuma R, Noguchi M, Ashizawa K, et al. Natural History of Pulmonary Subsolid Nodules: A Prospective Multicenter Study. J Thorac Oncol 2016;11:1012-28. [Crossref] [PubMed]
  10. Katsumata S, Aokage K, Nakasone S, et al. Radiologic Criteria in Predicting Pathologic Less Invasive Lung Cancer According to TNM 8th Edition. Clin Lung Cancer 2019;20:e163-70.
  11. Zhang Y, Fu F, Wen Z, et al. Segment Location and Ground Glass Opacity Ratio Reliably Predict Node-Negative Status in Lung Cancer. Ann Thorac Surg 2020;109:1061-8. [Crossref] [PubMed]
  12. Misaki N, Chang SS, Igai H, et al. New clinically applicable method for visualizing adjacent lung segments using an infrared thoracoscopy system. J Thorac Cardiovasc Surg 2010;140:752-6. [Crossref] [PubMed]
  13. Tarumi S, Misaki N, Kasai Y, et al. Clinical trial of video-assisted thoracoscopic segmentectomy using infrared thoracoscopy with indocyanine green. Eur J Cardiothorac Surg 2014;46:112-5. [Crossref] [PubMed]
  14. Okada M, Mimura T, Ikegaki J, et al. A novel video-assisted anatomic segmentectomy technique: selective segmental inflation via bronchofiberoptic jet followed by cautery cutting. J Thorac Cardiovasc Surg 2007;133:753-8. [Crossref] [PubMed]
  15. Sato M, Omasa M, Chen F, et al. Use of virtual assisted lung mapping (VAL-MAP), a bronchoscopic multispot dye-marking technique using virtual images, for precise navigation of thoracoscopic sublobar lung resection. J Thorac Cardiovasc Surg 2014;147:1813-9. [Crossref] [PubMed]
  16. Sekine Y, Koh E, Hoshino H. The efficacy of transbronchial indocyanine green instillation for fluorescent-guided wedge resection. Interact Cardiovasc Thorac Surg 2021;33:51-9. [Crossref] [PubMed]
  17. Kim Y, Rho J, Quan YH, et al. Simultaneous visualization of pulmonary nodules and intersegmental planes on fluorescent images in pulmonary segmentectomy. Eur J Cardiothorac Surg 2020;58:i77-84. [Crossref] [PubMed]
  18. Horinouchi H, Nomori H, Nakayama T, et al. How many pathological T1N0M0 non-small cell lung cancers can be completely resected in one segment? Special reference to high-resolution computed tomography findings. Surg Today 2011;41:1062-6. [Crossref] [PubMed]
  19. Xie D, Wu J, Hu X, et al. Uniportal versus multiportal video-assisted thoracoscopic surgery does not compromise the outcome of segmentectomy. Eur J Cardiothorac Surg 2021;59:650-7. [Crossref] [PubMed]
  20. Chen YY, Huang WL, Chang CC, et al. Uniportal versus Multiportal Thoracoscopic Complex Segmentectomy: Propensity Matching Analysis. Ann Thorac Cardiovasc Surg 2021;27:237-43. [Crossref] [PubMed]
  21. Numajiri K, Matsuura N, Igai H, et al. Uniportal thoracoscopic pulmonary segmentectomy provides good perioperative results and early postoperative recovery. J Thorac Dis 2022;14:2908-16. [Crossref] [PubMed]
Cite this article as: Matsuura N, Yajima T. Pulmonary segmentectomy for early stage non-small cell lung cancer: when, for which cases and how. J Thorac Dis 2023;15(3):956-959. doi: 10.21037/jtd-23-66

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