Elsevier

Lung Cancer

Volume 42, Issue 3, December 2003, Pages 297-301
Lung Cancer

Clinical value of video-assisted thoracoscopy for preoperative staging of non-small cell lung cancer: A prospective study of 105 patients

https://doi.org/10.1016/j.lungcan.2003.06.001Get rights and content

Abstract

This study prospectively evaluated the usefulness of thoracoscopy for staging non-small cell lung cancer in 105 consecutive patients. A comparison was made of TNM stage grouping classification according to clinical disease, thoracoscopic data, and pathological findings. In 40 (38%) patients, thoracoscopy was unreliable for assessing extent of disease due to pleural symphysis. In 13 T1 clinical lesions, thoracoscopy was unreliable in 5, clinical and thoracoscopic staging concurred in 4, but 4 cases changed to T2. In 62 T2 clinical lesions, thoracoscopy was not feasible due to technical difficulties in 21 (34%); however, in the remaining 41 cases, 6 lesions changed to T3 and 1 to T4. In the group of 23 T3 or T doubtful clinical disease, thoracoscopy was conclusive, whereas in 12 T4 clinical lesions, thoracoscopy contributed for tailoring treatment strategies. With regard to N stage, 72 N0 clinical cases, thoracoscopy revealed false negatives in 25%. N1 clinical lesions were not evaluated due to the small number of patients. In 30 N2 clinical lesions, thoracoscopy was incomplete in 11. In another 11 cases, mediastinal node involvement at nodal groups not accessible by mediastinoscopy was confirmed by thoracoscopy. Clinical and thoracoscopic findings were not concurrent in eight cases, therefore in clinical N2 lesions, the diagnostic accuracy of thoracoscopy was 63%. Only one case of unsuspected pleural metastasis was detected. Thoracoscopy-related complications occurred in nine cases. In summary, video-assisted thoracoscopy was useful for staging T3, T4, and T doubtful clinical disease as well as N2 lesions especially for the surgical exploration of lymph nodes at the lower paratracheal level (region 4), aortopulmonary window (region 5), paraaortic (region 6), posterior subcarinal space (region 7), paraesophageal (region 8), and inferior pulmonary ligament (region 9).

Introduction

Exact preoperative staging is a prerequisite for establishing an adequate treatment plan for patients with bronchial carcinoma [1]. Computed tomographic (CT) scan of the chest is a common diagnostic modality for assessing the primary tumor (T stage) and regional lymph nodes (N stage). However, despite intensive use of CT scanning facilities, the true extent of intrathoracic disease is frequently underestimated [2], [3]. Mediastinal lymph node invasion is associated with a poor prognosis even in patients undergoing curative operative therapy [4], [5]. Although primary surgical resection may be justified for a selected group of patients with mediastinal distal paratracheal involvement, most patients are candidates for induction chemotherapy before evaluating operability [6], [7]. Mediastinoscopy is an important diagnostic tool in patients with mediastinal nodal disease, avoiding unnecessary exploratory thoracotomy or incomplete resections in technically unresectable tumors [8]. On the other hand, cervical mediastinoscopy is associated with difficulties in adequately appraising hilar and interlobar nodes, the aortopulmonary window, lower paratracheal lymph nodes, aortic nodes, and inferior mediastinal nodes [9]. Anterior mediastinoscopy or the Chamberlain procedure and extended cervical mediastinoscopy are useful for the evaluations of subaortic and paraaortic nodes, with advantages and limitations for the assessment of other node chains. In addition, accurate evaluation of the T status preoperatively allows correctly selecting patients for the most appropriate surgical approach.

Video-assisted thoracoscopy possess some unique capabilities as a staging procedure for lung cancer operations [10], [11]. It is the only modality that allows complete visualization of the pleural space, with the added potential of permitting inspection of both the parietal and visceral pleural surfaces, the aortic and mediastinal lymph nodes, and the pulmonary hilum. This study prospectively evaluated the usefulness of video-assisted thoracoscopy for staging non-small cell lung cancer, considering T status, N status, and M status independently.

Section snippets

Patients and methods

Between 1996 and 1998, a total of 17 hospitals constituted the Spanish Video-Assisted Thoracic Surgery Study Group, with the objective of developing a protocol for the study and treatment of lung cancer, in particular, to collect data prospectively from patients with bronchial carcinoma at different stages in order to assess the clinical value of video-assisted thoracoscopy in the study and treatment of the disease. Patients with histologically documented non-small cell lung cancer (previously

Results

A total of 135 protocols from patients with non-small cell lung cancer were reviewed. However, 30 patients were excluded because of lack of histopathologic confirmation of specimens obtained by thoracotomy or biopsy. Therefore, the study population consisted of 105 patients with definite non-small cell lung cancer and who underwent clinical and videothoracoscopic lung cancer staging. Ninety patients (86%) underwent thoracotomy. The tumor was considered unresectable in four patients due to

Discussion

There is an increasing demand for accurate preoperative staging of bronchial carcinoma with respect to determination of tumor stage and nodal status. Video-assisted thoracoscopy provides an opportunity for evaluation and biopsy within the pleural space and at the pulmonary hilum. Most studies have shown that diagnostic accuracy of CT scan for lung cancer staging is lower than 60% [2], [5]. Systemic or selective mediastinoscopy allows visualization of nodes in the pretracheal, paratracheal and

Acknowledgements

This study was supported by Xunta de Galicia, Spanish Foundation of Pneumology and Thoracic Surgery (SEPAR), and Ethicon Endosurgery (Madrid, Spain). We are indebted to Javier Muñiz, MD, and Alfonso Castro, MD, Instituto de Ciencias de la Salud de A Coruña, for their contribution in data collection, and Marta Pulido, MD, for editing the manuscript and editorial assistance.

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Members: J.J. Rivas (general co-ordinator) and M. Deu, Hospital Miguel Servet, Zaragoza, A. Benı́tez, Hospital Carlos Haya, Málaga; A. Blanco, Hospital Virgen del Rocı́o, Sevilla; E. Canalı́s, Hospital Clı́nic, Barcelona; M. Carbajo, Hospital Universitario Marqués de Valdecilla, Santander; J. Freixinet, Hospital Dr. Negrı́n, Las Palmas de Gran Canaria; G. Gómez, Hospital de Sant Pau, Barcelona; F. Heras, Hospital Universitario de Valladolid, Valladolid; M. Jiménez, Hospital Universitario de Salamanca, Salamanca; E. Martı́n, Hospital Virgen de la Candelaria, Santa Cruz de Tenerife; M. Mateu, Hospital Mútua de Terrassa, Terrassa, Barcelona; L. Molins, Hospital del Sagrat Cor, Barcelona; J. Pac, Hospital de Cruces, Barakaldo, Bizkaia; Yat-Wah Pun, Hospital de la Princesa, Madrid; F. Sebastián-Quetglás, Hospital Universitari Josep Trueta, Girona; M. de la Torre, Hospital Juan Canalejo, A Coruña; and A. Torres, Hospital San Carlos, Madrid, Spain.

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