Methods: Between January 2004 and October 2005, 92 patients with non-small cell lung cancer (NSCLC) who underwent cervical video mediastinoscopy were included in this prospective study. Tissue biopsy samples and FNAs were obtained from the same lymph node and were sent for a pathologic examination. Tissue samples and FNAs were stained with Hematoxilene-Eosine. All specimens were evaluated by two histopathologists.
Results: Using tissue biopsy samples, no metastasis was found in 54 patients, while 38 patients were metastatic. Forty-eight patients had no metastasis, while 44 patients were metastatic using FNA samples. The difference was statistically non-significant (p>0.05). The false negativity of the FNA and tissue biopsy were 5.4% and 12%, respectively. Subsequently, 43 patients with negative FNA and tissue biopsy underwent lung resection with thoracotomy and sistematic lymph node dissection. Following lymph node dissection, lymph node metastases were found in two cases (4.6%). As a result, false negativity of mediastinoscopy was reduced to 4.6% when two techniques were combined. There was no complication related to the technique.
Conclusion: The FNA of mediastinal lymph nodes is a safe and effective method, compared to tissue biopsy and reduces the false negativity of mediastinoscopy when combined with tissue biopsy.
We have designed a prospective study in order to compare the results of FNA and tissue biopsy of lymph nodes during mediastinoscopy performed for lung cancer staging and combined them with the results for decreasing the number of false negative results of mediastinoscopy.
The statistical analysis was done by using the Statistical Package for the Social Sciences (SPSS Inc., Chicago, Illinois, USA) version 11.5 software. Differences between groups were calculated using McNemar’s test. The concordance of biopsy and cytology methods for the whole study group and cell type was assessed with “kappa” statistics. A p value (p<0.05) was considered significant in all statistical analysis.
Table 1: The numbers of lymph node cytology and biopsy
The difference was not statistically significant (McNemar’s test p=0.332). The combined results of FNA and tissue biopsy are shown in Table 2. It was also found that the results were highly comparable (k=0.705 and p<0.05). There was no morbidity or mortality related to either procedure.
Table 2: Histopathological results of lymph nodes (k=0.705; p<0.05)
Non-invasive methods, such as CT and PET, do not provide sufficient information on N2-N3 disease.[1] Suzuki et al.[9] showed that in patients with NSCLC and N0-N1 disease on the CT scan, mediastinoscopy revealed 17.9% N2 disease despite a negative CT scan. The mediastinal lymph nodes can be surgically staged by using mediastinoscopy, mediastinotomy, or thoracoscopy, or even by performing a thoracotomy. Mediastinoscopy, which allows direct visualization and localization of most superior, anterior subcarinal, and hilar nodes, has been regarded as the “gold standard” for staging of the mediastinum and has excellent access to stations 2R, 4R, 4L, 2L, and 7 along with the anterior subcarinal stations. The diagnostic value of the technique has been reported as between 83-89% in lung cancer patients whereas access to the main or lower aspect of the subcarinal lymph nodes is limited.[2,10-12] As an alternative to mediastinoscopy, endoscopic US-guided FNAs[7,10,13] or CT-fluoroscopy-guided[14] FNAs have been developed which have had an impact on lung cancer staging by facilitating access to virtually all mediastinal lymph node stations. Diagnostic yields of up to 90% have been seen. Wieserma et al.[15] demonstrated that endoscopic US-guided FNAs are safe and accurate for evaluating mediastinal lymph nodes arising in the lower paratracheal, subcarinal, aortopulmonary, and posterior regions. Endoscopic US-guided FNAs had a sensitivity of 96% and a specificity of 100%. However, these procedures require expensive and specific tools and devices.
In 1927, Dudgeon and Patric[16] described the use of cytology procedures for the rapid diagnosis of tumors in the operating room. It has also been shown in several studies that FNAs performed through the tracheobronchial wall, esophagus, or chest wall are safe and reliable and also provide high accuracy and similar false negative rates compared to mediastinoscopies.[10-12,15,17] Cytological or histological confirmation of malignancy and accurate tumor, node, and metastasis staging is critical for the delivery of effective lung cancer management.[18] Cytodiagnosis is useful for small specimens but not suitable for tissue block and has the advantage of easy preparation. Cytopathological methods are quicker, simpler, and more efficient and should be the option of choice when multiple samples are submitted for analysis within a short period of time. Thus, intraoperative cytology using FNAs has been preferred for many years in the histopathologic diagnosis of lesions from different organs.[4] In cytological examinations, the quality of results depends on the skill of the surgeon and the level of cytopathologic expertise.[17] Therefore, we have added FNAs of mediastinal lymph nodes during mediastinoscopy in order to obtain aspiration material from the whole lymph node and to reach the posterior subcarinal lymph nodes. Although tissue biopsies yielded metastases in 38 (41%) patients, FNAs diagnosed metastases in 44 (48%) patients. The false negative rate was 12% for the tissue biopsy group and 6% for the FNA group. The reduced false negative rate may be explained by having at least two samples aspirated from each lymph node and by the evaluation of posterior subcarinal lymph nodes. In FNAs, the needle also travels from the top to the bottom of the lymph node (a needle can be pushed up to the distal end of the lymph nodes). In open biopsies, it is very difficult and sometimes impossible to sample the distal side of the lymph node. When the process was repeated in different directions, we could take biopsies from different parts of the lymph node. Therefore, needle aspiration scans the lymph nodes in a broad spectrum. Fine needle aspiration failed to diagnose only two 4R lymph nodes that were found to be positive during thoracotomy. The combination of two techniques resulted in reduced N2 disease found during the surgery and increased surgical rates following induction chemotherapy at our center.
In conclusion, FNAs of mediastinal lymph nodes during mediastinoscopy is simple, reliable, and accurate while also being less time-consuming and less laborintensive. It has also proven to be useful for the intraoperative evaluation of mediastinal lymph nodes in lung cancer and should be added to the standard tissue biopsy during mediastinoscopy in order to select patients who will benefit from curative intent surgery.
Declaration of conflicting interests
The authors declared no conflicts of interest with respect
to the authorship and/or publication of this article.
Funding
The authors received no financial support for the
research and/or authorship of this article.
1) Larsen SS, Vilmann P, Krasnik M, Dirksen A, Clementsen
P, Skov BG, et al. Endoscopic ultrasound guided biopsy
versus mediastinoscopy for analysis of paratracheal and
subcarinal lymph nodes in lung cancer staging. Lung Cancer
2005;48:85-92.
2) Rintoul RC, Skwarski KM, Murchison JT, Wallace WA,
Walker WS, Penman ID. Endobronchial and endoscopic
ultrasound-guided real-time fine-needle aspiration for
mediastinal staging. Eur Respir J 2005;25:416-21.
3) Lemaire A, Nikolic I, Petersen T, Haney JC, Toloza EM,
Harpole DH Jr, et al. Nine-year single center experience with
cervical mediastinoscopy: complications and false negative
rate. Ann Thorac Surg 2006;82:1185-9.
4) Orki A, Tezel C, Kosar A, Ersev AA, Dudu C, Arman
B. Feasibility of imprint cytology for evaluation of
mediastinal lymph nodes in lung cancer. Jpn J Clin Oncol
2006;36:76-9.
5) Fritscher-Ravens A, Soehendra N, Schirrow L, Sriram
PV, Meyer A, Hauber HP, et al. Role of transesophageal
endosonography-guided fine-needle aspiration in the
diagnosis of lung cancer. Chest 2000;117:339-45.
6) Vilmann P, Larsen SS. Endoscopic ultrasound-guided biopsy
in the chest: little to lose, much to gain. Eur Respir J
2005;25:400-1.
7) Wallace MB, Silvestri GA, Sahai AV, Hawes RH, Hoffman
BJ, Durkalski V, et al. Endoscopic ultrasound-guided fine
needle aspiration for staging patients with carcinoma of the
lung. Ann Thorac Surg 2001;72:1861-7.
8) Vollmer RT, Herndon JE 2nd, D’Cunha J, Abraham NZ,
Solberg J, Fatourechi M, et al. Immunohistochemical detection
of occult lymph node metastases in non-small cell lung cancer:
anatomical pathology results from Cancer and Leukemia
Group B Trial 9761. Clin Cancer Res 2003;9:5630-5.
9) Suzuki K, Nagai K, Yoshida J, Nishimura M, Takahashi K,
Nishiwaki Y. Clinical predictors of N2 disease in the setting
of a negative computed tomographic scan in patients with
lung cancer. J Thorac Cardiovasc Surg 1999;117:593-8.
10) Zwischenberger JB, Savage C, Alpard SK, Anderson CM,
Marroquin S, Goodacre BW. Mediastinal transthoracic
needle and core lymph node biopsy: should it replace
mediastinoscopy? Chest 2002;121:1165-70.
11) Kramer H, van Putten JW, Post WJ, van Dullemen HM,
Bongaerts AH, Pruim J, et al. Oesophageal endoscopic
ultrasound with fine needle aspiration improves and simplifies
the staging of lung cancer. Thorax 2004;59:596-601.
12) Eloubeidi MA, Cerfolio RJ, Chen VK, Desmond R, Syed S,
Ojha B. Endoscopic ultrasound-guided fine needle aspiration
of mediastinal lymph node in patients with suspected lung
cancer after positron emission tomography and computed
tomography scans. Ann Thorac Surg 2005;79:263-8.
13) White P Jr, Ettinger DS. Tissue is the issue: is endoscopic
ultrasonography with or without fine-needle aspiration
biopsy in the staging of non-small-cell lung cancer an
advance? Ann Intern Med 1997;127:643-5.
14) White CS, Weiner EA, Patel P, Britt EJ. Transbronchial
needle aspiration: guidance with CT fluoroscopy. Chest 2000;118:1630-8.
15) Wiersema MJ, Vazquez-Sequeiros E, Wiersema LM.
Evaluation of mediastinal lymphadenopathy with endoscopic
US-guided fine-needle aspiration biopsy. Radiology
2001;219:252-7.
16) Paulose RR, Shee CD, Abdelhadi IA, Khan MK. Accuracy
of touch imprint cytology in diagnosing lung cancer.
Cytopathology 2004;15:109-12.