Robotic lung segmentectomy for malignant and benign lesions
Original Article

Robotic lung segmentectomy for malignant and benign lesions

Alper Toker, Kemal Ayalp, Elena Uyumaz, Erkan Kaba, Özkan Demirhan, Suat Erus

Department of Thoracic Surgery, Istanbul Bilim University and Group Florence Nightingale, Istanbul, Turkey

Correspondence to: Suat Erus, MD. Naima sokak No: 4/7 Yeşilköy, 34149 Istanbul, Turkey. Email: suaterus@gmail.com.

Objective: Surgical use of robots has evolved over the last 10 years. However, the academic experience with robotic lung segmentectomy remains limited. We aimed to analyze our lung segmentectomy experience with robot-assisted thoracoscopic surgery.

Methods: Prospectively recorded clinical data of 21 patients who underwent robotic lung anatomic segmentectomy with robot-assisted thoracoscopic surgery were retrospectively reviewed. All cases were done using the da Vinci System. A three incision portal technique with a 3 cm utility incision in the posterior 10th to 11th intercostal space was performed. Individual dissection, ligation and division of the hilar structures were performed. Systematic mediastinal lymph node dissection or sampling was performed in 15 patients either with primary or secondary metastatic cancers.

Results: Fifteen patients (75%) were operated on for malignant lung diseases. Conversion to open surgery was not necessary. Postoperative complications occurred in four patients. Mean console robotic operating time was 84±26 (range, 40-150) minutes. Mean duration of chest tube drainage and mean postoperative hospital stay were 3±2.1 (range, 1-10) and 4±1.4 (range, 2-7) days respectively. The mean number of mediastinal stations and number of dissected lymph nodes were 4.2 and 14.3 (range, 2-21) from mediastinal and 8.1 (range, 2-19) nodes from hilar and interlobar stations respectively.

Conclusions: Robot-assisted thoracoscopic segmentectomy for malignant and benign lesions appears to be practical, safe, and associated with few complications and short postoperative hospitalization. Lymph node removal also appears oncologically acceptable for early lung cancer patients. Benefits in terms of postoperative pain, respiratory function, and quality of life needs a comparative, prospective series particularly with video-assisted thoracoscopic surgery.

Keywords: Lung resection; robotic surgery; segmentectomy; lung cancer


Submitted Feb 26, 2014. Accepted for publication Jun 06, 2014.

doi: 10.3978/j.issn.2072-1439.2014.06.40


Introduction

Anatomic segmentectomy of the lung is the removal of a segment of the lobe. For many decades pulmonary segmentectomy has been used for the treatment of bronchiectasis and tuberculosis via thoracotomy. Recently, with the developments in video instrumentation and refinements in surgical techniques, segmentectomy has been a popular approach with video-assisted thoracic surgery (VATS). It has been preferred for tumors smaller than 2 cm and negative lymph nodes (1,2) and for larger tumors in patients with poor pulmonary function who could not tolerate lobectomy, especially those who do not have visceral pleural invasion (2,3). Although VATS has been used for segmentectomy for the past 5 years, robotic anatomic lung segmentectomy has been reported to be feasible only in two articles in the pubmed search (4,5).

As an academic thoracic surgery center performing minimally invasive anatomical lung resections with VATS for 8 years, we have recently developed a robotic surgery program with the da Vinci Robotic System (Intuitive Surgical, Inc, Mountain View, California, USA) which started on October 2011. In this study we aimed to analyze the segmentectomy operations performed for various etiologies.


Patients and methods

From the prospectively recorded database, anatomical segmentectomy patients’ data was retrieved. The data was analyzed for age, gender, etiology, pulmonary function tests, complications, mortality, duration of chest tube and duration of postoperative hospital stay. The number of mediastinal lymph node stations dissected and the number of dissected lymph nodes in patients with either primary or secondary lung cancer were also analyzed. For metastasectomies only single lesions close to the segmentary bronchus and primary lung cancer smaller than 2 cm were candidates for robotic segmentectomy operations (Figure 1). Patients who had primary lung tumors larger than 2 cm but smaller than 4.5 cm (2 patients) with compromised pulmonary functions were also underwent robotic common basal segmentectomy operations. According to our protocol; all patients who had an indeterminate nodule, or proven lung cancer or a possible metastatic lung cancer, had a PET-CT. Mediastinoscopy was reserved only for the patient who had a possible brain metastases.

Figure 1 (A) The CT shows an 84-year-old male with squamous cell carcinoma who previously had colon carcinoma; (B) the CT shows a 37-year-old male admitted with hemoptysis, after bronchoscopy revealed no pathology. He underwent a left lower lobe common basal segmentectomy with the diagnosis of echinococcus alveolaris; (C) the CT shows a 67-year-old male with a history of undiagnosed cerebral mass of 1 cm. He underwent mediastinoscopy and resection of superior segment of right upper lobe. Pathology revealed adenocarcinoma.

Robotic operations for indeterminate nodules were performed after localization of the nodule either with operative view (retraction of visceral pleura), after palpation with finger prior to the docking without access thoracotomy, or from 3 dimensional (3D) images of chest tomography.

All operations were performed by a single console surgeon (AT). All patients had anatomical segment resections as described below. Chest tubes were removed during the hospital stay if the length of stay was shorter than 5 days. If the drainage lasted longer and patients did not have any other problems (one patient), then the patients were discharged with chest tubes attached to the Heimlich valve.

Surgical technique

The patient was positioned on lateral decubitus position. The table was tilted either anteriorly or posteriorly depending on the type of segmentectomy operation to be performed. For superior segments of both lower lobes and posterior segment of the right upper lobe anterior tilt was preferred. For the resection of other segments a posterior tilt was preferred. Three ports were opened while trying to keep 10 cm between each port and 10 to 15 cm from the target which was hilum of the lobe containing the segment to be resected. The camera was placed in the middle port. The robot was docked from the posterior of the patient with 30 to 45 degrees between the vertebral column of the patient and transverse axis of the cart (Figure 2).

Figure 2 Docking of da Vinci. Arm numbers should be seen by the surgeon 1 at the table (arrows). The transverse axis of the da Vinci approaches from posterior of the patient with 30 to 45 degrees to vertebral column of the patient. 1, surgeon responsible from docking (may shift to console); 2, assistant surgeon is responsible for service, retraction, clipping and stapling; 3, nurse position.

With the robotic camera in up position, ports and instruments were placed and pleural symphyses were divided. Service port was performed at 10th-11th intercostal space at the posterior part of the thoracic wall. The rest of the operation was done with the camera in down position. Maryland or curved bipolar forceps for right arm and prograsper for left arm were used as needed. Segmentectomies were performed by dissecting the fissure and removing the nodes around the segmentary artery and bronchus. Arteries and veins were clipped with Hem-o-Lok (Teleflex Medical, Research Triangle Park, NC) or stapled with a vascular stapler. Bronchus was always stapled (Figures 3-5). Imaginary intersegmental plane was stapled after ventilating and deflating the remnant lung. In none of the patients, glues or sealants were used. Chest was closed by placing a single 28 F chest tube from the camera port.

Figure 3 Resection for a lingual sparing left upper lobectomy needs division of the superior segmentary vein, and proximal arteries to the left upper lobe and apicoposterior segment of the upper lobe bronchus.
Figure 4 Robotic right lower lobe superior segmentectomy (6).
Figure 5 Robotic mediastinal lymph node dissection (7).

Pain management

Routine pain management was with intercostal blocks to two intercostal spaces upper and two intercostal spaces lower around the ports (not more than 20 mL Marcaine) (Astra Zeneca, Istanbul) and 1 gram perfalgan (Bristol-Myers Squibb, New York City) intravenous infusion every 6 hours, and voltaren SR 75 mg (Novartis, Basel) are given through intramuscular route twice a day until chest tube is removed. After the removal of the chest tube or discharge of the patient oral medication with paracetamol and non-steroid anti-inflammatory drugs were given. Visual Analog Scale (VAS) was recorded by the anesthesiologists at 48 hours after the operation and by surgical team on postoperative day 15 as a part of data collection for possible evaluation of our pain management approach.


Results

The mean age was 59 (range, 28-84) years. Twenty-one segmentectomies, 10 from the right lung and 11 from the left lung were performed. Eight patients had a segmentectomy from the upper lobes and 13 patients from the lower lobes. Common basal segmentectomy (eight patients) and superior segmentectomy of the lower lobes (five patients) were the most commonly employed segmentectomies. Mean duration of console time was 84±26 (range, 40-150) minutes. Mean force expiratory volume (FEV1) in the first second was 2,278±662 (range, 1,274-4,870) mL. The mean duration of chest tube drainage and postoperative hospital stay were 3±2.1 (range, 1-10) and 4±1.4 (range, 2-7) days respectively. Conversion to open surgery was not necessary. Postoperative complications occurred in four patients (19%). The prolonged air leak (>5 days) was the cause of morbidity in all patients. None of the patients experienced a major cardiopulmonary complication. The mean number of mediastinal stations and number of dissected lymph nodes were 4.2 and 14.3 (range, 2-21) lymph nodes from mediastinal stations and 8.1 (range, 2-19) lymph nodes from hilar and interlobar stations, respectively. VAS was 3.4 and 1.4 on postoperative day 2 and day 15 (Table 1). The mean diameters of the malignant lesions were 1.9 (range, 1-4.3) cm. There were eight (72.7%) adenocarcinoma histology including five patients with lepidic pattern as the most common primary lung cancer. Eight patients (72.7%) out of 11 primary lung cancer were recorded to be in stage 1A. Six patients were operated on for benign diseases (bronchiectasis one patient, granuloma four patients and echinococcus alveolaris one patient). Four patients had segmentectomy operation for single pulmonary metastases (three patients for colon carcinoma and one patient for uterus leiomyoma).

Table 1
Table 1 Data of patients who underwent pulmonary segmentectomy operation
Full table

Discussion

VATS segmentectomy has been proved to be a safe procedure with fewer complications and a reduced hospital stay when compared with an open segmentectomy (8). The peri-operative outcome, including operative time, blood loss, duration of chest tube drainage and length of hospital stay, have been shown to be similar in another comparative study (9). This study also demonstrated that thoracoscopic segmentectomy is feasible with regard to peri-operative and oncological outcomes for Stage IA non-small cell lung cancer (NSCLC), especially T1a and carefully selected T1b descriptor (9). Thoracoscopic segmentectomy has been compared to thoracoscopic lobectomy when analyzing oncologic results in small (≤2 cm) peripheral stage IA NSCLC (10). Local recurrence rates with thoracoscopic segmentectomy (5.1%) have been reported to be similar to the thoracoscopic lobectomy (4.9%). No significant difference has been observed in 5-year overall or disease-free survival (10). Recent literature also demonstrated support for less invasive video thoracoscopic surgical techniques in pulmonary segmentectomy operations like uniportal and total thoracoscopic segmentectomies (11,12).

It is clear that, as lung screening programs increase around the world, the need for minimally invasive segmentectomies is also increasing. Certainly, robotic lung segmentectomies might be another minimally invasive lung segment resection technical option.

Growing knowledge of robotic lobectomies for lung cancer would provide additional experience for performing segmentectomy operations for lung cancer. Yet, there are only two articles published to assess the feasibility of robotic segmentectomy operation (4,5). In one of them Dylewski et al. (5) reported 35 segmentectomy patients and in the other Pardolesi et al. (4) reported 17 segmentectomy patients. Mean duration of surgery was reported to be 189 minutes with no major intraoperative complications and conversion to open procedure was reported as unnecessary (4). In this study postoperative morbidity rate was 17.6% with a median postoperative stay of 5 (range, 2-14) days, and postoperative mortality was 0% (4). The final pathology was reported to be NSCLC in eight patient, typical carcinoids in two, and lung metastases in seven. Because the other study (5) described a robotic series of almost 200 patients with mainly lobectomies, we do not have a detailed data regarding to segmentectomy operations.

Our indications and perioperative and postoperative outcomes are quite similar to those of Pardolesi and colleagues (4). In our experience, 15 out of 21 patients (75%) were operated on for malignant lung diseases. Conversion to open surgery was not necessary. Postoperative complications occurred in four patients (19%). Mean console robotic operating time was 84±26 (range, 40-150) minutes which was quite similar to that of Dylewski’s experience (5). The duration of our console time was shorter than the reported experiences even with VATS. Mean duration of chest tube drainage and postoperative hospital stay were 3±2.1 (range, 1-10) and 4±1.4 (range, 2-7) days respectively, which was also quite similar to the above mentioned study (4). The mean number of mediastinal stations and number of dissected lymph nodes were 4.2 and 14.3 (range, 2-21) lymph nodes. From hilar and interlobar stations, a mean of 8.1 (range, 2-19) lymph nodes were dissected in patients primary or secondary lung cancer. We need to stress that, five of our patients were not good candidates for lung resection due to compromised pulmonary, renal and cardiac problems. But we did not experience any adverse event in those patients. Our surgical technique demonstrated similarities with those of Pardolesi’s (4). However, our access port, similar in size to their experience (4), was located at posterior thoracic cavity at 10th-11th intercostal space. This port may not only have allowed the greater movement of the equipment within the cavity but also may have avoided the disturbance of the mammary gland in female patients. In our experience, we used only one Maryland forceps or curved bipolar forceps and one Prograsper forceps for each patient. Expenditures for these including the drapes cost a total of 600 USD, excluding the maintenance and initial costs of the robot.

The major difficulty in robotic segmentectomy operation is the resection without palpation. This could be overcome by palpating and tattooing the lesion prior to the implementation of the robotic arms. If this was not possible, 3D images could be used to identify the lesion, the vessels and the bronchus. Segmentectomy operation with robotic surgery requires a good knowledge of the anatomy of pulmonary vessels and bronchi in each patient (13). The foreknowledge of the anatomy of each patient would contribute to the safety and accuracy of the operation (13). It has been reported that presurgical planning based on patient’s actual 3D pulmonary model was useful for patients with stage IA NSCLC ≤2 cm in diameter and for selecting an appropriate VATS lung resection for an individual (14). Apparently, this may be a required preoperative technique in robotic segmentectomy as well. Although we only had three patients with this preoperative investigation, we discussed with experienced radiologists before each operation to delineate the borders of resection from axial, coronal and sagittal tomographies. Especially for metastasectomies, we believe that CT image evaluation on monitor with a qualified radiologist is essential to ensure that the lesion is solitary.

Robotic segmentectomy may provide better dissection capabilities around smaller vessels and the lymph nodes around lobar and segmentary bronchi. However, developing these techniques may require preparation and patience to overcome the difficulties of a correct docking, developing dissection techniques.

Yet, the provided data and results about performing robotic segmentectomies may not fully satisfy the thoracic surgical community. However, we have demonstrated that the robotic anatomic lung segmentectomy is a feasible and safe procedure with an acceptable operating time, adequate lymph node dissection, less pain and few complications.


Acknowledgements

Authors’ Contribution: A.T. designed the overall study with contributions from K.A. K.A. designed and carried out experiments, collected data. E.U. designed and carried out experiments and collected and analyzed data with E.K. and Ö.D. S.E. carried out experiments, and analyzed data with A.T.

Disclosure: The authors declare no conflict of interest.


References

  1. Keenan RJ, Landreneau RJ, Maley RH Jr, et al. Segmental resection spares pulmonary function in patients with stage I lung cancer. Ann Thorac Surg 2004;78:228-33; discussion 228-33. [PubMed]
  2. Koike T, Yamato Y, Yoshiya K, et al. Intentional limited pulmonary resection for peripheral T1 N0 M0 small-sized lung cancer. J Thorac Cardiovasc Surg 2003;125:924-8. [PubMed]
  3. Wolf AS, Richards WG, Jaklitsch MT, et al. Lobectomy versus sublobar resection for small (2 cm or less) non-small cell lung cancers. Ann Thorac Surg 2011;92:1819-23; discussion 1824-5.
  4. Pardolesi A, Park B, Petrella F, et al. Robotic anatomic segmentectomy of the lung: technical aspects and initial results. Ann Thorac Surg 2012;94:929-34. [PubMed]
  5. Dylewski MR, Ohaeto AC, Pereira JF. Pulmonary resection using a total endoscopic robotic video-assisted approach. Semin Thorac Cardiovasc Surg 2011;23:36-42. [PubMed]
  6. Toker A, Ayalp K, Uyumaz E, et al. Robotic right lower lobe superior segmentectomy. Asvide 2014;1:245. Available online: http://www.asvide.com/articles/257
  7. Toker A, Ayalp K, Uyumaz E, et al. Robotic mediastinal lymph node dissection. Asvide 2014;1:246. Available online: http://www.asvide.com/articles/258
  8. Leshnower BG, Miller DL, Fernandez FG, et al. Video-assisted thoracoscopic surgery segmentectomy: a safe and effective procedure. Ann Thorac Surg 2010;89:1571-6. [PubMed]
  9. Yamashita S, Tokuishi K, Anami K, et al. Thoracoscopic segmentectomy for T1 classification of non-small cell lung cancer: a single center experience. Eur J Cardiothorac Surg 2012;42:83-8. [PubMed]
  10. Zhong C, Fang W, Mao T, et al. Comparison of thoracoscopic segmentectomy and thoracoscopic lobectomy for small-sized stage IA lung cancer. Ann Thorac Surg 2012;94:362-7. [PubMed]
  11. Gonzalez-Rivas D, Fieira E, Mendez L, et al. Single-port video-assisted thoracoscopic anatomic segmentectomy and right upper lobectomy. Eur J Cardiothorac Surg 2012;42:e169-71. [PubMed]
  12. Ramos R, Girard P, Masuet C, et al. Mediastinal lymph node dissection in early-stage non-small cell lung cancer: totally thoracoscopic vs thoracotomy. Eur J Cardiothorac Surg 2012;41:1342-8; discussion 1348. [PubMed]
  13. Ikeda N, Yoshimura A, Hagiwara M, et al. Three dimensional computed tomography lung modeling is useful in simulation and navigation of lung cancer surgery. Ann Thorac Cardiovasc Surg 2013;19:1-5. [PubMed]
  14. Kanzaki M, Kikkawa T, Shimizu T, et al. Presurgical planning using a three-dimensional pulmonary model of the actual anatomy of patient with primary lung cancer. Thorac Cardiovasc Surg 2013;61:144-50. [PubMed]
Cite this article as: Toker A, Ayalp K, Uyumaz E, Kaba E, Demirhan Ö, Erus S. Robotic lung segmentectomy for malignant and benign lesions. J Thorac Dis 2014;6(7):937-942. doi: 10.3978/j.issn.2072-1439.2014.06.40

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