eISSN: 1897-4252
ISSN: 1731-5530
Kardiochirurgia i Torakochirurgia Polska/Polish Journal of Thoracic and Cardiovascular Surgery
Current issue Archive Manuscripts accepted About the journal Supplements Editorial board Reviewers Abstracting and indexing Contact Instructions for authors Publication charge Ethical standards and procedures
Editorial System
Submit your Manuscript
SCImago Journal & Country Rank
2/2020
vol. 17
 
Share:
Share:
Original paper

Is video-assisted thoracoscopic surgery sufficient for lymph node dissection in pulmonary metastasectomy?

Tayfun Kermenli
1

  1. Department of Thoracic Surgery, Istanbul Aydın University, Istanbul, Turkey
Kardiochir Torakochir Pol 2020; 17 (2): 61-64
Online publish date: 2020/07/20
Article file
- Is video-assisted.pdf  [0.12 MB]
Get citation
 
PlumX metrics:
 

Introduction

Among the primary features of malignant tumors are metastases that form in distant organs. It is reported that approximately 30% of patients receiving oncological treatment develop primary tumor-induced pulmonary metastasis [1]. Pulmonary metastasectomy is considered part of the treatment in these patients and has become recommended in many types of tumors. Thus, it has been shown that there is an increase in overall survival and disease-free survival times [2]. On the other hand, presence of mediastinal or hilar lymph node metastasis is also important in terms of prognosis especially in tumors of epithelial origin [3]. However, controversy continues about the mediastinal and hilar lymph node dissection application with pulmonary metastasectomy. There are publications reporting that mediastinal lymph node sampling is sufficient, as well as studies reporting that lymph node dissection should be performed [4, 5]. Performing lymph node dissection or sampling enables the detection of unexpected lymph node involvement and is useful in the postoperative therapeutic decision making process [6].

Presence of mediastinal and hilar lymph nodes can be detected by preoperative imaging methods such as computed tomography (CT) or positron emission tomography (PET)-CT prior to pulmonary metastasectomy [7]. Especially the findings suggesting the presence of malignant lymph node in preoperative PET-CT are guiding in terms of lymph node dissection [8]. In the preoperative evaluation, lymph node sampling or dissection may not be performed in patients without lymph node presence. However, although there are negative findings in PET-CT, there are publications reporting that unexpected lymph node positivity has been detected [9]. For this reason, mediastinal lymph node sampling or dissection is recommended during pulmonary metastasectomy.

Aim

It is known that microscopic disease in the mediastinal or hilar lymph nodes may be overlooked in imaging methods in patients undergoing pulmonary metastasectomy. In this study, we evaluated the results of patients undergoing pulmonary metastasectomy with video-assisted thoracoscopic surgery (VATS) and aimed to investigate postoperative lymph node positivity after lymph node dissection (PM-LND).

Material and methods

Patients who underwent pulmonary metastasectomy and mediastinal lymph node dissection with VATS between March 2015 and March 2020 in our clinic were included in the study. Presence of mediastinal and hilar lymph node metastases was evaluated in patients with planned pulmonary metastasectomy by CT. The lymph nodes with a short axis over 1 cm and a long axis over 2 cm were considered positive in the mediastinum, and these patients underwent PET-CT staging, thus scanning for distant metastases. Intraabdominal organ metastases were investigated with abdominal CT and pelvic CT. Patients with a suspicious appearance below 1 cm in thorax CT were referred to metastasectomy. Patients with the maximum standard uptake value (SUVmax) of 2.5 and above involvement in lymph node in PET-CT were excluded from the study. These patients were directed to an interventional procedure for mediastinal sampling.

Invasive staging was performed by video-mediastinoscopy or mediastinotomy. In our hospital, these procedures were not used for staging since endobronchial ultrasound and endoscopic ultrasound biopsy could not be performed. Metastasectomy was planned for patients with lymph node involvement in PET-CT with an SUVmax below 2.5 or negative in the lymph node staging biopsy. Inclusion and exclusion criteria are given in Table I.

Table I

Inclusion and exclusion criteria

Inclusion criteriaExclusion criteria
1. Resectable single or multiple pulmonary metastasis
2. Patients whose respiratory capacity is suitable for lung resection
3. The presence of lymph node under 1 cm in thorax CT and with benign appearance
4. Lymph node SUVmax uptake value < 2.5 in PET-CT
5. Negative result in invasive staging of the lymph node
6. Cases operated with VATS
1. Unresectable pulmonary metastasis
2. Patients whose respiratory capacity is not suitable for surgery
3. Presence of non-lung distant metastasis in abdomen and pelvic CT
4. Lymph node SUVmax uptake value ≥ 2.5 in PET-CT
5. Tumor positivity in invasive staging of the lymph node
6. Cases operated by thoracotomy

Results

As a result of the preoperative evaluation, the procedure was performed with VATS in all patients who were eligible for VATS. Patients who underwent PM-LND with thoracotomy were not included in the study. The mean age of 58 patients who underwent pulmonary metastasectomy and mediastinal lymph node dissection with VATS was 56.5 ±10.7 (40–74). Thirty-four of the patients were female (58.6%) and 24 were male (41.4%). A total of 61 surgical procedures, 3 of which were bilateral, were performed in 58 patients. The procedure was performed in the same session in 3 patients who underwent bilateral pulmonary metastasectomy and lymph node dissection.

The number of patients who underwent invasive mediastinal lymph node biopsy due to suspicious lymph node positivity in the preoperative period was 13, of which 11 were video-mediastinoscopy and 2 were left anterior mediastinotomy. Anatomical resection (lobectomy: 1, segmentectomy: 3) was performed in 4 (6.6%) of 61 surgical procedures, and wedge resection was performed in 57 (93.4%) patients (Table II).

Table II

Patients’ demographics

ParameterN%
Age56.5 ±10.7
GenderMale2441.4
Female3458.6
Surgery sideRight3051.7
Left2543.1
Bilateral35.2
Resection type
(n = 61)
Anatomic46.6
Non-anatomic
(Wedge resection)
5793.4
Number of resected metastases1.72 ±1.01
Number of dissected lymph nodes3.1 ±0.97

The mean number of resected pulmonary metastases was 1.72 ±1.01 (1–5). The total number of dissected lymph nodes was 191, with an average of 3.1 ±0.97 (2–6) per surgical procedure (Table III). Colon ca (20 patients, 34.4%) and breast ca (16 patients 27.6%) were the most common primary tumor origin. Others were thyroid (n = 9, 15.5%), sarcoma (n = 9, 15.5%), renal cell ca (n = 3, 5.2%) and melanoma (n = 1, 1.8%). Unexpected lymph node positivity was present in 9 of 58 patients (15.5%). Five of these patients were followed by breast ca and 4 were due to colon ca (Table IV). There were no patients who had positive postoperative lymph node after PM-LND in the preoperative period with mediastinotomy or video-mediastinoscopy.

Table III

Number of dissected lymph nodes and pathologic positive lymph nodes

Origin of primary
tumor
Dissected LNPathologic positive LN%
N1N2
Colorectal554211
Breast494518.3
Thyroid35
Sarcoma37
Renal cell11
Melanoma4
Table IV

Origin of pulmonary metastases

Origin of primary
tumor
Number
of patients
%LN positive
patients
%
Colorectal2034.4420
Breast1627.6531.2
Thyroid915.5
Sarcoma915.5
Renal cell35.2
Melanoma11.8

The average length of hospital stay of the patients was 3.1 ±0.83 (2–5) days. No mortality was observed in the patients within the first 30 days in the postoperative period. Postoperatively 6 (10.3%) patients had complications, atelectasis (n = 3, 5.1%), prolonged air leak (n = 2, 3.4%) and arrhythmia (n = 1, 1.8%) (Table V).

Table V

Postoperative complications

ComplicationsN%
Atelectasis35.1
Prolonged air leak23.4
Arrhythmia11.8

Discussion

Video-assisted thoracoscopic surgery has been used safely in lung surgery for many years [10]. Many complex lung procedures, including sleeve resections, have been performed with this technique in recent years [11, 12]. There were various drawbacks in the application of adequate lymph node dissection in patients undergoing VATS for lung cancer surgery. However, studies have shown that mediastinal lymph node dissection can be performed as effectively as thoracotomy with VATS [13, 14]. With videothoracoscopy being so usable, its rate in pulmonary metastasectomy has also increased gradually. The most important point in terms of pulmonary metastasectomy is the detection of the localization of the pulmonary nodules during VATS surgery. It was reported that this limitation of VATS was resolved by opening incisions suitable for the localization of metastatic nodules [15]. Khereba et al. [16] showed that it is useful in detecting intrathoracic lung ultrasonography (US) nodule localization during VATS. In these patients, there was a significant improvement in the rate of transition from VATS to thoracotomy with the use of intrathoracic US.

In our study, patients who underwent pulmonary metastasectomy and lymph node dissection with VATS were evaluated. Triportal VATS was used in all patients and incisions were opened in localizations to allow palpation of the nodule with a finger. All patients were evaluated by thorax CT in the preoperative period and metastasectomy was decided accordingly. PET-CT and invasive staging methods were used for staging purposes. Metastasectomy was not performed in patients with mediastinal lymph node positivity.

In our patient series, contrary to the literature, the rate of female patients was 58.6%. We think that, this is due to the fact that the patients with primary diagnosis of breast carcinoma were higher in our study compared to other studies in the literature. In many studies in the literature, male patients are the majority [1719]. As another feature of our study, when the primary origin of patients is examined, we see that the most common cases are colorectal carcinoma (34.4%). This rate is also seen to be compatible with the literature [20]. In second place is breast carcinoma; others were thyroid, sarcoma, renal cell ca and melanoma. In our series, there were no patients with primary gynecological carcinoma and head and neck carcinoma. In our hospital, gynecological oncology and oncological surgery of the head and neck region are not actively performed, so we think that we do not have any patients with these cell types.

It is known that lymph node dissection is a prognostic factor in terms of disease-free survival and overall survival rates in patients undergoing pulmonary metastasectomy. In meta-analyses of 4363 patients, Shiono et al. [21] showed that mediastinal lymph node positivity is a poor prognosis criterion. They reported that mediastinal lymph node sampling or dissection should be performed in their studies in which patients underwent lobectomy for pulmonary metastases. In patients who underwent pulmonary metastasectomy, the unpredictable lymph node positivity in the preoperative period is reported to be around 17% [22]. In our series, the mean number of resected metastases in our patients was 1.72, and the average number of lymph nodes dissected from the same patients was 3.1. Mediastinal or hilar lymph node positivity was detected in 9 of these patients. An unexpected lymph node positivity in 15.5% of 58 patients who underwent pulmonary metastasectomy and mediastinal lymph node dissection with VATS shows the importance of lymph node dissection in these patients. In this way, an effective oncological treatment plan can be made for the patients in the postoperative period. As a limitation of our study, the number of patients could not be evaluated in terms of survival between patients with negative lymph node and patients who were negative. There is also a need for randomized controlled trials to determine if there is any difference between lymph node dissection or sampling.

Conclusions

Video-assisted thoracoscopic surgery is a technique that can be applied in pulmonary metastasectomy with its advantages such as low complication rate and rapid recovery. During VATS, there will be no problem in palpating and detecting the nodule through incisions suitable for pulmonary nodule localization. In these patients, lymph node dissection, which is one of the determining factors of prognosis, can be performed effectively with VATS. Mediastinal and hilar lymph node dissection combined with pulmonary metastasectomy is effective in detecting unexpected lymph node positivity. Therefore, we think that lymph node dissection should be performed.

Disclosure

Author reports no conflict of interest.

References

1 

Rena O, Papalia E, Oliaro A, et al. Pulmonary metastases from epithelial tumours: late results of surgical treatment. Eur J Cardiothorac Surg 2006; 30: 217-222.

2 

Fournel L, Maria S, Seminel M, et al. Prognostic factors after pulmonary metastasectomy of colorectal cancers: a single-center experience. J Thorac Dis 2017; 9 (Suppl 12): S1259-1266.

3 

Sihag S, Muniappan A. Lymph node dissection and pulmonary metastasectomy. Thorac Surg Clin 2016; 26: 315-323.

4 

Pfannschmidt J, Klode J, Muley T, et al. Nodal involvement at the time of pulmonary metastasectomy: experience in 245 patients. Ann Thoracic Surg 2006; 81: 48-54.

5 

Reinersman JM, Wigle DA. Lymphadenectomy during pulmonary metastasectomy. Thorac Surg Clin 2016; 26: 35-40.

6 

Bölükbas S, Sponholz S, Kudelin N, et al. Risk factors for lymph node metastases and prognosticators of survival in patients undergoing pulmonary metastasectomy for colorectal cancer. Ann Thorac Surg 2014; 97: 1926-1932.

7 

Hamaji M, Cassivi SD, Shen KR, et al. Is lymph node dissection required in pulmonary metastasectomy for colorectal adenocarcinoma? Ann Thorac Surg 2012; 94: 1796-1800.

8 

Guerrera F, Mossetti C, Ceccarelli M, et al. Surgery of colorectal cancer lung metastases: analysis of survival, recurrence and re-surgery. J Thorac Dis 2016; 8: 1764-1771.

9 

Kim HK, Lee K, Han KN, et al. The predictive accuracy of sentinel nodes mapping in the setting of pulmonary metastasectomy. Clin Exp Metastasis 2017; 34: 125-131.

10 

Zhang J, Zhao H, Lv L, et al. Uniportal thoracoscopic pulmonary lobectomy in the treatment of lung cancer. Pak J Med Sci 2020; 36: 182-186.

11 

Sekhniaidze D, Gonzalez-Rivas D. Uniportal video-assisted thoracoscopic sleeve resection. Ann Cardiothorac Surg 2016; 5: 145-146.

12 

Czyżewski D, Wojtacha J, Filipowski M, et al. Videothoracoscopic surgery for primary spontaneous pneumothorax: our experience. Kardiochir Torakochirur Pol 2007; 4: 35-39.

13 

Ma L, Liu C, Mei J, et al. Video-assisted thoracoscopic surgery non-grasping en bloc mediastinal lymph node dissection for the right side. J Thorac Dis 2018; 10: 4502-4504.

14 

Nagashima T. Thoracoscopic left mediastinal lymph node dissection. Ann Transl Med 2016; 4: 10.

15 

Ambrogi V, Sellitri F, Perroni G, et al. Uniportal video-assisted thoracic surgery colorectal lung metastasectomy in non-intubated anesthesia. J Thorac Dis 2017; 9: 254-261.

16 

Khereba M, Ferraro P, Duranceau A, et al. Thoracoscopic localization of intraparenchymal pulmonary nodules using direct intracavitary thoracoscopic ultrasonography prevents conversion of VATS procedures to thoracotomy in selected patients. J Thorac Cardiovasc Surg 2012; 144: 1160-1165.

17 

Raza A, Takabe K, Wolfe LG, et al. Outcomes of hybrid video assisted thoracoscopic surgery for pulmonary metastasectomy. J Surg Sci 2014; 2: 18-24.

18 

Predina JD, Newton AD, Corbett C, et al. Near-infrared intraoperative imaging for minimally invasive pulmonary metastasectomy for sarcomas. J Thorac Cardiovasc Surg 2019; 157: 2061-2069.

19 

Hanna TP, Chauvin C, Miao Q, et al. Clinical outcomes after pulmonary metastasectomy for melanoma: a population-based study. Ann Thorac Surg 2018; 106: 1675-1681.

20 

Abdelnour-Berchtold E, Perentes JY, Ris HB, et al. Survival and local recurrence after video-assisted thoracoscopic lung metastasectomy. World J Surg 2016; 40: 373-379.

21 

Shiono S, Matsutani N, Okumura S, et al. The prognostic impact of lymph-node dissection on lobectomy for pulmonary metastasis. Eur J Cardiothorac Surg 2015; 48: 616-621.

22 

Seebacher G, Decker S, Fischer JR, et al. Unexpected lymph node disease in resections for pulmonary metastases. Ann Thorac Surg 2015; 99: 231-236.

Copyright: © 2020 Polish Society of Cardiothoracic Surgeons (Polskie Towarzystwo KardioTorakochirurgów) and the editors of the Polish Journal of Cardio-Thoracic Surgery (Kardiochirurgia i Torakochirurgia Polska). This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
 
Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.