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Eur J Cardiothorac Surg 2007;32:351-354. doi:10.1016/j.ejcts.2007.04.031
Copyright © 2007, European Association for Cardio-Thoracic Surgery. Published by Elsevier B.V. All rights reserved

The value of video-assisted mediastinoscopy in pulmonary metastasectomy

Ashvini Menon*, Richard Milton, James Andrew Charles Thorpe, Kostas Papagiannopoulos

St James University Hospital, Leeds, United Kingdom

Received 19 September 2006; received in revised form 10 April 2007; accepted 19 April 2007.

* Corresponding author. Address: 51 Tolkien Way, Hartshill, Stoke on Trent ST4 7SJ, Staffordshire, UK. Tel.: +44 7973674826; fax: +44 1706 646734. (Email: ashvinimenon{at}aol.com).


    Abstract
 Top
 Abstract
 1. Introduction
 2. Material and method
 3. Results
 4. Discussion
 Appendix A
 References
 
Objective: To assess the role of video-assisted mediastinoscopy (VAM) in identifying involved mediastinal lymph nodes in patients undergoing pulmonary metastasectomy. Methods: Over a 4-year period (2002–2005) a retrospective study was carried out in 57 patients (44 men, 13 women, mean age 59 years) undergoing isolated, unilateral or bilateral metastasectomy. Following staging CT scan, VAM was performed prior to open thoracotomy, median sternotomy or VATS resection of the metastasis. Follow-up was complete in all patients. Results: Fifty-seven patients underwent 62 operations for metastatic disease. The majority had colorectal cancer (39) followed by renal (11), sarcoma (9), liver (2) and miscellaneous (8). Six patients (10.5%) had positive mediastinal nodes on VAM. There was no perioperative morbidity or mortality. At a median follow-up of 25 months, 63 patients (68.5%) were still alive. Conclusions: Mediastinal lymph node involvement has been reported to occur in up to 14% of patients with pulmonary metastasis. In our study, 10% of patients treated for pulmonary metastasis had positive nodal disease at metastasectomy. We believe our results confirm that VAM can be safely performed and may have a role in more accurate staging of metastatic disease and influence the decision for post-resection adjuvant therapy.

Key Words: Video mediastinoscopy • Pulmonary metastasectomy • Mediastinal lymph nodes


    1. Introduction
 Top
 Abstract
 1. Introduction
 2. Material and method
 3. Results
 4. Discussion
 Appendix A
 References
 
Cervical mediastinoscopy remains an important investigation for nodal staging in lung cancer. Video-assisted mediastinoscopy (VAM) has further enhanced this investigation and is now widely used with a high sensitivity and specificity and low morbidity and mortality [1].

Metastasectomy has now been performed for a wide variety of primary tumours, e.g. renal cell carcinoma and colorectal carcinoma, with encouraging results [10]. Mediastinal lymph node involvement has been reported in up to 14% of patients undergoing thoracotomy for metastasectomy. The presence of lymph node metastases has an adverse effect on prognosis and influences the decision for adjuvant therapy [2,3].

The role of VAM in nodal staging of pulmonary metastases has not been fully evaluated. Therefore, we performed this study to assess the value of VAM in the assessment of mediastinal lymph nodes in patients with pulmonary metastasis.


    2. Material and method
 Top
 Abstract
 1. Introduction
 2. Material and method
 3. Results
 4. Discussion
 Appendix A
 References
 
A retrospective study of 57 patients who underwent 62 pulmonary metastasectomies from January 2002 to December 2005 was undertaken.

There were 44 men and 13 women with a mean age of 59 years. Five patients had sequential pulmonary metastasectomy. Seven patients were re-operated for recurrence of pulmonary metastasis.

Preoperative evaluation included physical examination, cardiopulmonary assessment, chest X-ray and computed tomography (CT) of chest and abdomen. All patients had no radiological evidence of primary disease at the time of pulmonary metastasectomy. Positron emission tomography (PET) scan was not performed at our institution during this time period, as it was not available.

VAM was performed in all patients regardless of radiological evidence of mediastinal lymphadenopathy. All samples were sent for routine histological evaluation.

All patients were followed up at 6 weeks and at 3 monthly intervals. Those with positive lymph nodes were offered adjuvant treatment.

2.1 Procedure
VAM was performed via a 3–4 cm transverse incision in the suprasternal notch and followed by blunt dissection down to the pretracheal space. A Karl–Storz video mediastinoscope was utilised. Blunt dissection was performed and any lymph nodes identified were biopsied and sent for histology labelled with the appropriate station level. The patient was then placed in the thoracotomy position and an open or VATS pulmonary metastasectomy was performed depending on the anatomical location of the lesion. Bilateral lesions were resected via median sternotomy or sequential thoracotomies depending on the surgeon's preference. The mediastinal lymph nodes were assessed for tumour spread to N2 lymph node station according to the International System for Staging of Lung Cancer.


    3. Results
 Top
 Abstract
 1. Introduction
 2. Material and method
 3. Results
 4. Discussion
 Appendix A
 References
 
VAM was performed in 57 patients. Six patients (10.5%) had metastatic mediastinal lymph node spread. Mediastinal lymph node metastasis was found in two patients with renal cell carcinoma and in one patient with colorectal cancer, bladder, breast and adrenal cancer respectively. One patient was found to have subcapsular deposit of metastatic cells from a primary adrenal tumour (paraganglioma). Subcarinal (7) and right paratracheal stations (R4) were the commonest sites of nodal involvement.

The primary site was predominantly colorectal in 39 patients (Table 1 ). One patient (2.6%) had positive mediastinal lymph node. This patient survived for 30 months following adjuvant chemotherapy. The disease-free interval for colorectal patients (from primary to lung) is 39.7 months.


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Table 1 Types of primary tumour site
 
There was no involvement of mediastinal lymph nodes in 49 patients (86%) and no obvious lymph nodes on biopsy in 2 patients.

The survival without adjuvant therapy in two patients with positive lymph nodes, one from renal cell carcinoma and the other bladder carcinoma, was 8 and 4 months respectively.

The surgical approach was mainly thoracotomy or VATS. Median sternotomy was performed for bilateral metastasectomy (Table 2 ).


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Table 2 Surgical approach to pulmonary metastasectomy
 
There was no mortality or morbidity for VAM in pulmonary metastasectomy.

Thirty-four patients (59.6%) are still alive. This is a heterogeneous group of patients with various pathologies, and, therefore, it would not be appropriate to apply any statistical analysis to this group. It is too early to produce an accurate Kaplan–Meier survival curve in this heterogeneous group of patients.


    4. Discussion
 Top
 Abstract
 1. Introduction
 2. Material and method
 3. Results
 4. Discussion
 Appendix A
 References
 
The surgical management of pulmonary metastases is a well-established modality with an overall survival of 36% and 26% at 5 and 10 years, respectively [4].

However, better survival figures are seen in renal cell carcinoma. Isolated pulmonary metastases from renal cell carcinoma can have up to 50% 5-year survival [5]. In recent years, increasing number of patients are presenting with colorectal carcinoma and lung metastases. Although there are emerging techniques like thoracoscopic photodynamic therapy (PDT) or radio frequency ablation (RFA), surgery remains the treatment of choice in most thoracic units.

The importance and frequency of nodal involvement in pulmonary metastasectomy has been an intriguing subject since 1950s. An autopsy series demonstrated a 33% incidence of mediastinal lymph node involvement in the presence of pulmonary metastases [6]. In recent years, several centres have demonstrated the presence of positive mediastinal lymph nodes via systematic mediastinal lymph node dissection at thoracotomy. The incidence of positive nodes ranged from 14 to 28% of patients [2,3], but no study has been performed to assess the role of mediastinoscopy. Therefore, since 2002, we elected to assess the role of VAM in our institution in pulmonary metastasectomy. At this time, routine PET scanning was not available.

In our study, the incidence of mediastinal lymph node metastases was 10%. This correlates with similar results from previous studies where systematic mediastinal lymph node dissection at operation was practised [2].

VAM is widely used by surgeons and trainees. It has high sensitivity and specificity, making it a reliable method for identifying diseased mediastinal lymph nodes. In our study, we had no morbidity or mortality. However, Ercan and colleagues have shown complications in 10% of their 70 patients who underwent complete mediastinal lymph node dissection at thoracotomy [3].

Several studies have suggested the use of mediastinoscopy in identifying metastatic lymph nodes in pulmonary metastasis [5]. Some centres have performed mediastinoscopy only in patients with CT evidence of mediastinal lymph node involvement [7]. However, the sensitivity of CT scan to correctly predict lymph node involvement is only 73% [8,9]. Loehe and colleagues have shown that the frequency of misdiagnosed mediastinal lymph node metastases in patients with pulmonary metastases is 17%, similar to non-small cell bronchial carcinomas [2]. PET scanning in the UK has now become a recommended preoperative investigation for patients with non-small cell bronchial carcinoma [9]. The role of PET scan in pulmonary metastasectomy remains unclear and requires further investigation. The current benefit of PET is restricted in identifying active primary site and extrathoracic metastases or positive mediastinal lymph nodes. This is where the role of VAM is essential in providing histological diagnosis. A suggestive flowchart for the management of pulmonary metastasectomy is recommended (Fig. 1 ).


Figure 1
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Fig. 1. Flowchart for the management of pulmonary metastasectomy.

 
Pulmonary metastasectomy is the subject of an ESTS working group which has not yet reported. Several studies have shown that the presence of lymph node metastases in pulmonary metastasectomy has an adverse effect on long-term survival [2,3]. However, there are no randomised trials to clearly define the role of surgery and adjuvant therapy in pulmonary metastasectomy. VAM may help in accurate staging of mediastinal lymph nodes in pulmonary metastasis.


    Appendix A
 Top
 Abstract
 1. Introduction
 2. Material and method
 3. Results
 4. Discussion
 Appendix A
 References
 
Conference discussion

Dr S. Mattioli (Bologna, Italy): Just a comment. I wonder if for soft tissue metastases VATS is truly a good indication, because those who have been doing this kind of surgery know that soft tissue tumors give the lung very little metastases, not even appreciable with a CAT scan, and palpation is a crucial maneuver in these tumors. Everybody knows about the Memorial randomized trial which was closed by Pat McCormack because of this reason. So this is my concern.

Dr P. Van Schil (Antwerp, Belgium): I think there is a bit of confusion. This paper mainly discusses mediastinal staging which was performed by video-mediastinoscopy and not by a VATS approach. In that respect, could you comment on which nodes were positive? Were they all on the ipsilateral side? Were there some contralateral positive nodes?

Dr Menon: They were ipsilateral nodes and they were R4 and subcarinal nodes that were positive.

Dr Van Schil: Did you also look at survival in those patients? Your conclusion is that those patients should not be operated upon, but is that a valid conclusion from the study you performed?

Dr Menon: As I say, we still should proceed to operate on these patients. That's why I said that if these nodes come back as positive, they should undergo metastasectomy as well as chemoradiation, because it has been shown in previous studies that metastasectomy improves survival in positive or negative nodes, but these patients should be subjected to chemoradiation as well.

Dr Van Schil: And regarding those patients who did not have a mediastinoscopy before the operation, were there any cases of N2 or N3 involvement that you detected during thoracotomy?

Dr Menon: No, we didn’t actually look at that.

Dr B. Witte (Koblenz, Germany): In the patients who were node-negative at videomediastinoscopy, you obviously did proceed to an open operation. Did you reassess the mediastinum by lymphadenectomy and did you find any overlooked positive nodes in them? To put it short, what was the false-negative rate of video-mediastinoscopy?

Dr Menon: No, we did the video-mediastinoscopy before we proceeded to the pulmonary metastasectomy, and we didn’t assess the other nodes at that time, so we didn’t do a mediastinal lymph node sampling during the time of thoracotomy.

Dr Witte: Oh, so it's not about accuracy data. I see.

Dr M. Zielinski (Zakopane, Poland): I have some concerns about your algorithm. I think that we should treat these patients in a very individual way. For example, if there is a single metastasis in the lung, in one lung, and during mediastinoscopy you find only one metastasis in one node, why not proceed to thoracotomy? Maybe you should perform metastasectomy, exploration of the lung, and lymphadenectomy and it might be a better solution than to refer the patient to chemoradiation in that case. So I think I would advise you to be more flexible in your qualifications.


    Footnotes
 
\#9734; Presented at the joint 20th Annual Meeting of the European Association for Cardio-thoracic Surgery and the 14th Annual Meeting of the European Society of Thoracic Surgeons, Stockholm, Sweden, September 10–13, 2006.


    References
 Top
 Abstract
 1. Introduction
 2. Material and method
 3. Results
 4. Discussion
 Appendix A
 References
 

  1. Van Schil PE, Van Hee RH, Schoofs EL. The value of mediastinoscopy in preoperative staging of bronchogenic carcinoma. J Thorac Cardiovasc Surg 1989;97(2):240-244.[Abstract]
  2. Loehe F, Kobinger S, Hatz RA, Helmberger T, Loehrs U, Fuerst H. Value of systematic mediastinal lymph node dissection during pulmonary metastasectomy. Ann Thorac Surg 2001;72:225-229.[Abstract/Free Full Text]
  3. Ercan S, Nichols III FC, Trastek VF, Deschamps C, Aleen MS, Miller DL, Schleck CD, Pairolero PC. Prognostic significance of lymph node metastasis found during pulmonary metastasectomy for extrapulmonary carcinoma. Ann Thorac Surg 2004;77:1786-1791.[Abstract/Free Full Text]
  4. The International Registry of Lung Metastases, Writing CommitteePastorino U, Buyse M, Friedel G, Ginsberg RJ, Girard P, Goldstraw P, Johnston M, McCormack P, Pass H, Putnam Jr. JB. Long-term results of lung metastasectomy: prognostic analyses based on 5206 cases. J Thorac Cardiovasc Surg 1997;113:37-49.[Abstract/Free Full Text]
  5. Murthy SC, Kim K, Rice TW, Rajeswaran J, Bukowski R, DeCamp MM, Blackstone EH. Can we predict long-term survival after pulmonary metastasectomy for renal cell carcinoma?. Ann Thorac Surg 2005;79:996-1003.[Abstract/Free Full Text]
  6. Abrams HL, Spiro R, Goldstein N. Metastases in carcinoma: analysis of 1000 autopsied cases. Cancer 1950;3:75-85.
  7. Pfannschmidt J, Klode J, Muley T, Dienemann H, Hoffmann H. Nodal involvement at the time of pulmonary metastasectomy: experiences in 245 patients. Ann Thorac Surg 2006;81:448-454.[Abstract/Free Full Text]
  8. Graham AN, Chan KJ, Pastorino U, Goldstraw P. Systematic nodal dissection in the intrathoracic staging of patients with non-small cell lung cancer. J Thorac Cardiovasc Surg 1999;117:246-251.[Abstract/Free Full Text]
  9. Weng E, Tran L, Rege S, Safa A, Sadeghi A, Juilard G, Mark R, Santiago S, Brown C, Mandelkern M. Accuracy and clinical impact of mediastinal lymph node staging with FDG-PET imaging in potentially respectable lung cancer. Am J Clin Oncol 2000;23:47-52.[CrossRef][Medline]
  10. Reddy RHV, Kumar B, Shah R, Mirsadraee S, Papagiannopoulos K, Lodge P, Thorpe JAC. Staged pulmonary and hepatic metastasectomy in colorectal cancer—is it worth it?. Eur J Cardiothorac Surg 2004;25:151-154.[Abstract/Free Full Text]



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