Robotic resection of stage III lung cancer: an international retrospective study
Editorial

Robotic resection of stage III lung cancer: an international retrospective study

Monica Casiraghi1, Lorenzo Spaggiari1,2

1Division of Thoracic Surgery, European Institute of Oncology, 2Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy

Correspondence to: Dr. Monica Casiraghi. Division of Thoracic Surgery, European Institute of Oncology, Via G. Ripamonti, 435 20141 Milan, Italy. Email: monica.casiraghi@ieo.it.

Provenance: This is an invited Editorial commissioned by the Section Editor Olivia Tilla Maria Lauk (University Hospital Zurich, Zurich, Switzerland).

Comment on: Veronesi G, Park B, Cerfolio R, et al. Robotic resection of Stage III lung cancer: an international retrospective study. Eur J Cardiothorac Surg 2018. [Epub ahead of print].


Submitted May 24, 2018. Accepted for publication Jul 12, 2018.

doi: 10.21037/jtd.2018.07.90


The minimally invasive approach in thoracic surgery has proven advantages in terms of reduced postoperative pain, shorter immune response, quicker resumption of daily activities, and better aesthetic and functional result (1-3). The minimally invasive surgery despite it is recognized by the majority of thoracic surgeons still has a slow diffusion due to the technical difficulty and the long-lasting learning curve (4-7). The result of this situation is that a large part of thoracic surgeons still prefers an open traditional approach to perform a lung anatomical resection. Surgical manipulation also exerts a depressing cell-mediated immunity, which is manifested through the alteration in the cell, activation and function of lymphocytes and monocytes. The magnitude of these effects is proportional to the extent of the surgical procedure.

One of the major criticisms of minimally invasive surgery was due to inadequate mediastinal lymph node dissection compared with thoracotomy procedures, usually related to greater operator discomfort and a partial view due to the position of the camera, in particular to perform radical lymphadenectomy. This concern over inferior oncologic outcomes has so far contributed to the slow adoption of minimally invasive surgery techniques. However, robot-assisted thoracic surgery (RATS) using the da Vinci system represented a technological evolution of the video-assisted thoracic surgery (VATS) procedure leading to a better view of the operative field (3D instead of 2D), a simpler use of the instruments, and more precise movements, even superior to the human hand (8-11). To address the limitations of conventional thoracoscopy, a tele-surgical system was developed to offer the surgeons several benefits, which include three-dimensional, high-definition imaging, and a greater free movement of the surgeon using wristed instruments and the master-slave surgical cart, and computer-assisted scaling down of motion and reduction of hand-related tremors (da Vinci system, Intuitive Surgical, Sunnyvale, CA, USA). This could offer to the surgeon an innovative approach to resect and stage lung cancer with a more precise dissection and with theoretically better oncological results. These improvements become particularly useful in case of advanced disease with lymph nodes involvement allowing an easier and safer N1 and N2 lymph node dissection (12-14). In the literature, different series showed higher number of harvest lymph nodes in RATS compare to VATS and similar to open surgery (13,14,15-18). Also overall pathologic lymph node upstaging for RATS (14.8–24%) was similar to the larger open series (14.3–24.6%) and better than conventional VATS (10.6–11.9%) (13,14,16-18).

However, the most common indication for minimally invasive approach in lung cancers with either VATS or RATS, are early stage non-small cell lung cancer (NSCLC) (stage I and II) (19). Despite some series report the use of robotic surgery in patients with both initial or locally advanced NSCLC (8-13), the results of this approach specifically for stage III disease have been described only in very limited retrospective studies (11,20-24), showing anyhow similar oncological outcomes between open and minimally invasive groups, in term of post-operative outcome and survival even after chemotherapy.

Veronesi et al. recently published a retrospective multicentre study describing one of the largest series of patients (n=223) with pN2 NSCLC and carcinoid undergoing RATS (25). In this study the author showed acceptable perioperative outcomes with only 2.7% of converted cases to open surgery due to bleeding demonstrating the safety and feasibility of the procedure, even in patients underwent induction chemotherapy. One of the major difficulty related to RATS is the lack of perception that can make surgery particularly challenging especially in the case of chemotherapy or radiotherapy, with higher risk of intra operative complications. However, in this series they highlighted that large tumor size and >2 positive lymph nodes were associated with higher risk of conversion to open surgery despite unexpected mediastinal nodal invasion as well as pre-operative treatments were not the major cause of thoracotomy conversion. In this important series, the estimated 3-year survival in NSCLC patients was 61.2%, showing an excellent oncological result even if it could be related by the fact that most of the patients (n=142/223; 63.7%) had occult N2 disease and only 34 (15%) patients underwent induction therapy.

Also in our recent series of 339 patients who underwent RATS for clinical stages I–II NSCLC, we showed an excellent overall lymph node upstaging (17.6%) and 58% of 5-year stage specific survival for occult pN2 patients (n=28) confirming that mediastinal lymph node dissection during RATS adequately assesses lymph node stations leading to excellent oncologic results (19).

In conclusion, RATS lung resection for advanced NSCLC is safe and feasible both in terms of post-operative outcome and oncological results. However, these results require prospective studies (ongoing our multicenter prospective study for stage IIIApN2 NSCLC) and further testing on a larger population to be validated.


Acknowledgements

None.


Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.


References

  1. Hoksch B, Ablassmaier B, Walter M, et al. Complication rate after thoracoscopic and conventional lobectomy. Zentralblatt fur Chirurgie 2003;128:106-10. [Crossref] [PubMed]
  2. Nomori H, Ohtsuka T, Horio H, et al. Difference in the impairment of vital capacity and 6-minute walking after a lobectomy performed by thoracoscopic surgery, an anterior limited thoracotomy, an antero-axillary thoracotomy, and a posterolateral thoracotomy. Surg Today 2003;33:7-12. [Crossref] [PubMed]
  3. Li WW, Lee RL, Lee TW, et al. The impact of thoracic surgical access on early shoulder function video-assisted thoracic surgery versus posterolateral thoracotomy. Eur J Cardiothorac Surg 2003;23:390-6. [Crossref] [PubMed]
  4. Daniels LJ, Balderson SS, Onaitis MW, et al. Thoracoscopic lobectomy a safe and effective strategy for patients with stage I lung cancer. Ann Thorac Surg 2002;74:860-4. [Crossref] [PubMed]
  5. McKenna RJ Jr, Houck W, Fuller CB. Video-assisted Thoracic Surgery Lobectomy: Experience with 1,100 cases. Ann Thorac Surg 2006;81:421-5; discussion 425-6. [Crossref] [PubMed]
  6. Whitson BA, D'Cunha J, Andre RS, et al. Thoracoscopic versus thoracotomy approaches to lobectomy: differential impairment of cellular immunity. Ann Thorac Surg 2008;86:1735-44. [Crossref] [PubMed]
  7. Park BJ, Flores RM, Rusch VW. Robotic assistance for video-assisted thoracic surgical lobectomy: technique and initial results. J Thorac Cardiovasc Surg 2006;131:54-9. [Crossref] [PubMed]
  8. Veronesi G, Galetta D, Maisonneuve P, et al. Four-arm robotic lobectomy for the treatment of early-stage lung cancer. J Thorac Cardiovasc Surg 2010;140:19-25. [Crossref] [PubMed]
  9. Zhao X, Qian L, Lin H, et al. Robot-assisted lobectomy for non-small cell lung cancer in china: initial experience and techniques. J Thorac Dis 2010;2:26-8. [PubMed]
  10. Melfi FM, Mussi A. Robotically assisted lobectomy: learning curve and complications. Thorac Surg Clin 2008;18:289-95. [Crossref] [PubMed]
  11. Dylewski MR, Ohaeto AC, Pereira JF. Pulmonary resection using a total endoscopic robotic video-assisted approach. Semin Thorac Cardiovasc Surg 2011;23:36-42. [Crossref] [PubMed]
  12. Cerfolio RJ, Bryant AS, Skylizard L, et al. Initial consecutive experience of completely portal robotic pulmonary resection with 4 arms. J Thorac Cardiovasc Surg 2011;142:740-6. [Crossref] [PubMed]
  13. Yang HX, Woo KM, Sima CS, et al. Long-term Survival Based on the Surgical Approach to Lobectomy For Clinical Stage I Nonsmall Cell Lung Cancer: Comparison of Robotic, Video-assisted Thoracic Surgery, and Thoracotomy Lobectomy. Ann Surg 2017;265:431-7. [Crossref] [PubMed]
  14. Park BJ, Melfi F, Mussi A, et al. Robotic lobectomy for non-small cell lung cancer (NSCLC): long-term oncologic results. J Thorac Cardiovasc Surg 2012;143:383-9. [Crossref] [PubMed]
  15. Toosi K, Velez-Cubian FO, Glover G, et al. Upstaging and survival after robotic-assisted thoracoscopic lobectomy for non-small cell lung cancer. Surgery 2016;160:1211-8. [Crossref] [PubMed]
  16. Lee BE, Korst RJ, Kletsman E, et al. Transitioning from video-assisted thoracic surgical lobectomy to robotics for lung cancer: are there outcomes advantages? J Thorac Cardiovasc Surg 2014;147:724-9. [Crossref] [PubMed]
  17. Merritt RE, Hoang CD, Shrager JB. Lymph node evaluation achieved by open lobectomy compared with thoracoscopic lobectomy for N0 lung cancer. Ann Thorac Surg 2013;96:1171-7. [Crossref] [PubMed]
  18. Licht PB, Jorgensen OD, Ladegaard L, et al. A national study of nodal upstaging after thoracoscopic versus open lobectomy for clinical stage I lung cancer. Ann Thorac Surg 2013;96:943-9. [Crossref] [PubMed]
  19. Casiraghi M, Galetta D, Borri A, et al. Ten Years' Experience in Robotic-Assisted Thoracic Surgery for Early Stage Lung Cancer. Thorac Cardiovasc Surg 2018. [Epub ahead of print]. [PubMed]
  20. Yan TD, Cao C, D'Amico TA, et al. Video-assisted thoracoscopic surgery lobectomy at 20 years: a consensus statement. Eur J Cardiothorac Surg 2014;45:633-9. [Crossref] [PubMed]
  21. Petersen RP, Pham D, Toloza EM, et al. Thoracoscopic lobectomy: a safe and effective strategy for patients receiving induction therapy for non-small cell lung cancer. Ann Thorac Surg 2006;82:214-8. [Crossref] [PubMed]
  22. Nakanishi R, Fujino Y, Yamashita T, et al. Thoracoscopic anatomic pulmonary resection for locally advanced nonsmall cell lung cancer. Ann Thorac Surg 2014;97:980-5. [Crossref] [PubMed]
  23. Hennon MW, Demmy TL. Video-assisted thoracoscopic surgery (VATS) for locally advanced lung cancer. Ann Cardiothorac Surg 2012;1:37-42. [PubMed]
  24. Park BJ, Yang HX, Woo KM, et al. Minimally invasive (robotic assisted thoracic surgery and video-assisted thoracic surgery) lobectomy for the treatment of locally advanced non-small cell lung cancer. J Thorac Dis 2016;8:S406-13. [Crossref] [PubMed]
  25. Veronesi G, Park B, Cerfolio R, et al. Robotic resection of Stage III lung cancer: an international retrospective study. Eur J Cardiothorac Surg 2018. [Epub ahead of print]. [Crossref] [PubMed]
Cite this article as: Casiraghi M, Spaggiari L. Robotic resection of stage III lung cancer: an international retrospective study. J Thorac Dis 2018;10(Suppl 26):S3081-S3083. doi: 10.21037/jtd.2018.07.90

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