Methods: A total of 239 patients (153 males, 86 females; mean age 53.3±13.7 years; range 14 to 85 years) who were diagnosed with or suspected to have lung cancer or mediastinal lymphadenopathy between January 2004 and December 2012 were performed transbronchial needle aspiration rapid on-site cytologic evaluation. Diagnosis success, localization and size of lymph nodes, and number of sampling were analyzed.
Results: Diagnostic specimens were obtained from a total of 227 patients (93.03%) and 297 lymph nodes were sampled. A statistically significant difference was detected between lymph node stations and dimensions (p=0.018). Subcarinal lymph nodes had the highest diagnosis rate (91.5%) and 49.5% of these were benign. Mean lymph node diameters were 23.9±10.4 mm in malignant group (n=123), 19.4±7.4 mm in benign group (n=135), and 19.1±8.8 mm in undiagnosed group (n=39) and the diameters were statistically significantly different from each other (p=0.001). A repeat transbronchial needle aspiration was performed in five patients and no metastasis was detected in three of them. All negative results (n=12) were confirmed with histopathological examination after resection.
Conclusion: On-site evaluation decreases the risk of inadequate specimens and increases diagnostic accuracy rate of transbronchial needle aspiration. Transbronchial needle aspiration may be the initial procedure of choice while staging lung cancer or diagnosing mediastinal lymph node. Procedure may be performed by thoracic surgeons in the operating room in patients planned for mediastinoscopy.
Surgical resection is considered as the best treatment method in NSCLC; however, clinical evidence indicates that patients with mediastinal lymph node (MLN) metastasis have poor prognosis.[2,3] Therefore, accurate MLN staging is critical for selecting patients suitable for surgery.[4] Mediastinoscopy remains the gold standard for mediastinal staging of NSCLC, but this procedure is associated with certain complications, such as bleeding, recurrent nerve damage, and thoracic duct injury. Particularly, remediastinoscopy after neoadjuvant chemotherapy or chemo-radiotherapy for N2 disease have a higher complication rate than mediastinoscopy.[6,7] Transbronchial needle aspiration and rapid on-site cytologic evaluation (TBNA-ROSE) might be the first choice for staging N2 disease to avoid complications of redo-mediastinoscopy in NSCLC.
Occasionally, establishing a diagnosis might be challenging in some patients with centrally located NSCLC without an endobronchial component and TBNA-ROSE may be used as a diagnostic procedure in such tumors.[6] Therefore, in this study, we aimed to assess the role and efficiency of TBNA accompanied by ROSE performed in the operating room in patients who are planned to undergo mediastinoscopy.
Preoperative investigations included medical history, physical examination, hemogram, routine blood chemistry, electrocardiogram, posteroanterior and lateral chest radiograms, computed tomographic scans of the chest, and positron emission tomographycomputed tomography (PET-CT). When enlarged mediastinal/hilar lymph nodes (10 mm or more in the shortest axis) or a central lung or mediastinal mass were detected in CT scans, TBNA-ROSE was performed for staging and/or diagnosis.
All patients were informed about the intervention and explained that if a diagnosis was established with TBNA-ROSE, the procedure was going to be ended; otherwise, mediastinoscopy would be conducted in the same session. This retrospective study was approved by the Ethics Committee of Ankara University.
Major complications were defined as hemorrhage causing surgical exploration, pulmonary embolus, and myocardial infarction. Minor complications were minimal hemorrhage and pneumothorax.
We performed the TBNA-ROSE procedure under general anesthesia, using laryngeal mask airway (LMA). We preferred LMA because it permitted the needle aspiration of the upper paratracheal nodes. Aspirations were performed using a video flexible bronchoscope. All specimens were obtained through a flexible videobronchoscope using a standard, retractable 22 or 21-gauge cytology needle or a 19-gauge histology needle (ANSO-19, 21, 22-W Horizons International Corp., Barreal de Heredia, Costa Rica). The specific site from which the aspirate was obtained (subcarinal, paratracheal, hilar etc.) and number of sampling were recorded in every case.
No further intervention was carried out when the disease was diagnosed with TBNA-ROSE. But mediastinoscopy was performed if there was any suspicion for lymphoma or in undiagnosed cases.
One experienced cytopathologist evaluated all cytopathological samples on-site. The aspirated materials were immediately smeared onto glass slides, air-dried and immediately stained with Diff-Quik (Thermo Fisher Scientific, Waltham, MA, USA) for the interpretation to confirm adequate cell material. Furthermore, additional air dried and 95% of ethanol fixed wet smears were prepared and stained with May-Grünwald Giemsa and Papanicolaou stain for routine cytopathological evaluation. If possible, the rest of the material (loose microtissue cores) on the glass slide was transferred into 10% buffered formalin solution with assistance of a needle tip and processed as cell block for histological examination. When the cytological material was considered adequate, the procedure was terminated. Multiple passes were performed for each targeted site until on-site assessment was diagnostic for a disease process or an adequate sample was obtained.
If numerous benign lymphoid cell or clusters of anthracotic pigment laden macrophages with scattered lymphoid cells were present, or if a specific cytopathological diagnosis could be rendered, aspirated material were considered as satisfactory for cytological evaluation. The ROSE results were compared with the corresponding results of the final pathologic diagnosis. Immunohistochemistry was also carried out in some patients. A reference standard was established for the final diagnosis. The patients with benign lymphadenopathy or mass were followed-up for at least 12 months for any clinical or radiological evidence of disease progression. In patients with malignant lymphadenopathy or mass, the determination of final status of the lesion was based on malignant cytological results at TBNAROSE, with a subsequent clinical course consistent with malignant disease. Transbronchial needle aspiration and ROSE diagnosis was confirmed by biopsy during thoracotomy in NSCLC patients with negative TBNA results.
Statistical analysis
Patients were evaluated for diagnosis success,
LN localization and size, and number of sampling.
Sensitivity, specificity, and accuracy of localization and
size of MLNs were calculated. Distributions of these
variables were compared between groups and between
cell types using the chi-square test and Fisher’s exact test
for qualitative variables. Age analyses were performed
using Student’s t-test. All data comparisons and analyses
were performed using SPSS for Windows version 10.0
software program (SPSS Inc., Chicago, IL, USA).
Data were expressed as mean ± standard deviation and
differences were considered as statistically significant
when the p value was less than 0.05.
Mediastinoscopy (n=6) or mini thoracotomy (n=4) was performed in 10 cases in the undiagnosed group at the same session (malign, n=3; benign, n=7). No other procedures were carried out in the remaining seven patients as they refused any further interventions. In ROSE, 17 TBNA specimens were inadequate for diagnosis, but on final cytopathologic examination, one of them could be yielded with definitive diagnosis. In our series, overall discordance of preliminary and final diagnoses was 0.4% (1 out of 244 procedures).
In 239 patients, 297 LNs were sampled with TBNA and evaluated with ROSE. The characteristics of sampled lymph nodes are demonstrated in Table 1. Subcarinal station was the most punctured site (67.3%). A statistically significant difference was found between LN stations and dimensions (p=0.018); while the paratracheal MLN group had the largest mean LN size, the pretracheal MLN group had the smallest mean LN size (p=0.002). In all LN stations, results of TBNA were 45.5% (n=135) benign, 41.4% (n=123) malignant, and 13.1% (n=39) undiagnosed. Our success rate was 86.9% in TBNA results of LNs. Subcarinal station had the best diagnosis rate (91.5%) as well as the highest benign rate (49.5%). Paratracheal stations had the highest malignancy rate (60%) and the lowest benign disease rate (20%). Subcarinal position of LN was a predictor of positive aspirates and paratracheal LN station was a predictor of malignant disease. In ROSE, sampled materials in 39 cases (13.1%) were inadequate for diagnosis. There was a high failure rate (24.3%) in sampling of upper MLN stations.
Table 1: Characteristics of sampled lymph nodes
The mean diameter of the lymph node in short axis was 21.2±9.2 mm (range, 8-60 mm) on CT image. The mean diameters were 23.9±10.4 mm in malignant group (n=123), 19.4±7.4 mm in benign group (n=135), and 19.1±8.8 mm in undiagnosed group, indicating a statistically significant difference among the groups. When each group was compared to each other, there was a statistically significant difference (malignant vs. benign p=0.001, malignant vs. undiagnosed p=0.006 and benign vs. undiagnosed p=0.5). The diameters of the malignant LNs were larger than the others. There was a correlation between the lymph node size and malignancy.
Multiple passes were performed until on-site evaluation was judged as diagnostic. The number of needle passes required for successful lymph node sampling was 2.8±2 in total, 2.5±1.6 in malignant group, and 2.6±2.2 in benign group, whereas it was 4.4±2 in undiagnosed group (Table 2). In our study, the threshold of needle passes for diagnosis was 2.5 and its sensitivity, specificity, and area under curve (AUC) were 60%, 87%, and 79%, respectively. When the relationship between character of the disease and the number of needle passes were evaluated, a statistically significant difference was found (p=0.001). When each group was compared to the others, the difference between the undiagnosed and the other two groups was statistically significant (malignant vs. undiagnosed, p=0.001 and benign vs. undiagnosed, p=0.001). The number of needle passes for the diagnosis of sampling of malignant disease was lower than in benign disease. Our study also showed that positive LN was easier to diagnose than benign LN but there was no statistically significant difference (malignant vs. benign p=0.5).
Table 2: Relationship between number of sampling and lymph node location
Mediastinal staging of NSCLC was performed in 64 patients with TBNA-ROSE, which resulted in a change of therapy recommendation from curative surgery to neo-adjuvant chemotherapy or curative chemo-radiotherapy. Nine patients underwent curative surgery after negative results of final TBNA evaluation for MLN metastases. All these negative results were confirmed with final histopathological examination after curative surgery. Re-TBNA-ROSE was performed in five patients after neoadjuvant chemotherapy and three of them were detected as negative with TBNA. All the negative results were also confirmed with final histopathological examination during resection materials. Two cases had persistent N2 disease in MLN staging with TBNA. Negative results of TBNA evaluation of 12 cases were confirmed with histopathological examinations after curative surgery. One patient with renal failure had a minor complication (hemorrhage); however, there was no major complication in our interventions.
In recent years, many authors clearly demonstrated the improved diagnostic accuracy of real-EBUS-guided TBNA, but equipment for EBUS-TBNA is costly and therefore is not available in every hospital.[8-11] However, TBNA-ROSE can be performed in every hospital with a thoracic surgeon and cytopathologist. Baram et al.[1] and Diette et al.[2] reported that on-site cytopathology assessment was associated with greater diagnostic success. The results of a randomized trial that evaluated the utility of ROSE for the diagnosis of adenopathy using TBNA showed that ROSE significantly reduces the number of TBNAs and the complication rate of the bronchoscopy with TBNA.[5,12] Our TBNA-ROSE procedures were performed under general anesthesia with the use of a laryngeal mask airway and intravenous anesthesia as in EBUS-TBNA.[13] We have successfully performed TBNA-ROSE on 244 procedures without any major complications thanks to the procedure itself or general anesthesia.
Mediastinal staging is of importance for planning the treatment of NSCLC patients but mediastinoscopy allows access to only a limited number of MLN stations[1,2,3,4,7]. Transbronchial needle aspiration is less invasive than mediastinoscopy and allows access to a wider range of MLN stations[2,3,4,7,10,11].[14] In our series, mediastinal staging of NSCLC was performed in 64 patients with TBNA-ROSE, which resulted in the change of therapy recommendation from curative surgery to neo-adjuvant chemotherapy or curative chemo-radiotherapy.
A number of imaging techniques, including multislice CT, 18-fluoro-deoxyglucose positron emission tomography-PET, and integrated PETCT have recently been developed to investigate the mediastinum.[15,16] However, reliance on imaging alone is unacceptable and tissue diagnosis is still required to guide management.[17,18] Therefore, re-mediastinal staging after induction therapy is necessary for selecting the appropriate treatment strategy, but redo mediastinoscopy after induction therapy may be inaccurate.[19] The first mediastinoscopy might cause local fibrosis and adhesions, which make it technically difficult to perform re-mediastinoscopy. These problems may be overcome by EBUS or TBNA-ROSE especially for mediastinal staging after neoadjuvant chemotherapy. Transbronchial needle aspiration and ROSE may be a safer alternative modality for MLN sampling before or after induction therapy. In our series, re-TBNA-ROSE was performed in five patients after neoadjuvant chemotherapy and three of them had negative results. We operated on three patients and their N2 stations were histopathologically negative. Our limited experience has shown that the re-TBNAROSE may be safely performed for re-mediastinal staging in NSCLC.
The utility of TBNA-ROSE has been previously reported and it has been shown that at least five to seven TBNA needle passes would be needed to achieve a plateau diagnostic yield.[20,21] In our study, the number of needle passes required for successful lymph node sampling was 2.8±2 in total, 2.5±1.6 in malignant disease, and 2.6±2.2 in benign disease; however, this number was 4.4±2 in undiagnosed group (Table 2). Our threshold of needle passes for diagnosis was 2.5 and its sensitivity, specificity and AUC were 60%, 87%, and 79%, respectively. The number of needle passes did not correlate with the diagnosis after the fourth pass. The TBNA-ROSE significantly improves the diagnostic yields and also reduces the number of passes necessary for achieving high diagnostic yields.[1,12] Conversely, EBUS-TBNA samples are often difficult to interpret because of the low quality of samples. The amount of lymphoid tissue depends not only on the technical aspect but also on cellularity of the lymph node.[22] Endobronchial ultrasound and TBNA can evaluate the morphologic features of LN but not the cellularity of the lymph node; therefore, ROSE may be preferred for determining the adequacy of TBNA with or without EBUS samples by the presence of normal lymphocytes, especially for non-malignant lymph nodes. In this study, adequate or diagnostic specimens were determined in 93.03% (n=227) of the procedures with TBNAROSE. Transbronchial needle aspiration and ROSE is a valuable method for identifying good quality samples.
Endobronchial ultrasound is a new and promising TBNA technique for improving diagnostic yield; however, ROSE not only improves the yield of procedure but also enables triage of material to secondary investigations (i.e. culture, flow cytometry).[23] From this point of view, ROSE is an important part of TBNA or EBUS-TBNA for diagnosing tissues and staging lung cancer.
However, the importance of improving the performance of TBNA through education and experience cannot be completely overemphasized, we believe that these factors really lead an significant role for improving.[1,24] Rapid on-site cytopathological evaluation decreases the frequency of inadequate specimens and increases diagnostic accuracy of TBNA.[1,6,24]
In conclusion, transbronchial needle aspiration rapid on-site cytologic evaluation was shown to be an easy and rapid technique with good outcomes and reduced the number of mediastinoscopy procedures. In our series, mediastinoscopy was prevented in 222 (92.9%) of 239 patients. Transbronchial needle aspiration and rapid on-site cytologic evaluation with or w ithout endobronchial ultrasound may be t he initial procedure of choice by thoracic surgeons in the staging or diagnosing of the mediastinal lymph node or mass before mediastinoscopy.
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) Baram D, Garcia RB, Richman PS. Impact of rapid on-site
cytologic evaluation during transbronchial needle aspiration.
Chest 2005;128:869-75.
2) Diette GB, White P Jr, Terry P, Jenckes M, Rosenthal D,
Rubin HR. Utility of on-site cytopathology assessment for
bronchoscopic evaluation of lung masses and adenopathy.
Chest 2000;117:1186-90.
3) Baram D. Comparison of the diagnostic accuracy of
transbronchial needle aspiration for bronchogenic carcinoma
and other malignancies. J Bronchol 2004;11:87-91.
4) Nakajima T, Yasufuku K, Saegusa F, Fujiwara T, Sakairi Y,
Hiroshima K, et al. Rapid on-site cytologic evaluation during
endobronchial ultrasound-guided transbronchial needle
aspiration for nodal staging in patients with lung cancer. Ann
Thorac Surg 2013;95:1695-9.
5) Iyoda A, Baba M, Shibuya K, Moriya Y, Yasufuku K, Sekine
Y, et al. Transbronchial fine needle aspiration cytological
examination: a useful tool for diagnosing primary lung cancer.
Thorac Cardiovasc Surg 2006;54:117-9.
6) Yasufuku K, Fujisawa T. Staging and diagnosis of non-small cell
lung cancer: invasive modalities. Respirology 2007;12:173-83.
7) Kunst PW, Lee P, Paul MA, Senan S, Smit EF. Restaging of
mediastinal nodes with transbronchial needle aspiration after
induction chemoradiation for locally advanced non-small cell
lung cancer. J Thorac Oncol 2007;2:912-5.
8) Holty JE, Kuschner WG, Gould MK. Accuracy of transbronchial
needle aspiration for mediastinal staging of non-small cell
lung cancer: a meta-analysis. Thorax 2005;60:949-55.
9) Krasnik M, Vilmann P, Larsen SS, Jacobsen GK. Preliminary
experience with a new method of endoscopic transbronchial
real time ultrasound guided biopsy for diagnosis of mediastinal
and hilar lesions. Thorax 2003;58:1083-6.
10) Herth FJ. Mediastinal staging--the role of endobronchial and
endo-oesophageaL sonographic guided needle aspiration. Lung Cancer 2004;45:63-7.
11) Yasufuku K, Nakajima T, Motoori K, Sekine Y, Shibuya K,
Hiroshima K, et al. Comparison of endobronchial ultrasound,
positron emission tomography, and CT for lymph node staging
of lung cancer. Chest 2006;130:710-8.
12) Trisolini R, Cancellieri A, Tinelli C, Paioli D, Scudeller L,
Casadei GP, et al. Rapid on-site evaluation of transbronchial
aspirates in the diagnosis of hilar and mediastinal adenopathy:
a randomized trial. Chest 2011;139:395-401.
13) Sarkiss M, Kennedy M, Riedel B, Norman P, Morice R,
Jimenez C, et al. Anesthesia technique for endobronchial
ultrasound-guided fine needle aspiration of mediastinal lymph
node. J Cardiothorac Vasc Anesth 2007;21:892-6.
14) Groth SS, Andrade RS. Endobronchial and endoscopic
ultrasound-guided fine-needle aspiration: a must for thoracic
surgeons. Ann Thorac Surg 2010;89:2079-83.
15) Vansteenkiste J, Dooms C. Positron emission tomography in
nonsmall cell lung cancer. Curr Opin Oncol 2007;19:78-83.
16) Gonzalez-Stawinski GV, Lemaire A, Merchant F, O’Halloran
E, Coleman RE, Harpole DH, et al. A comparative analysis
of positron emission tomography and mediastinoscopy in
staging non-small cell lung cancer. J Thorac Cardiovasc Surg
2003;126:1900-5.
17) De Leyn P, Stroobants S, De Wever W, Lerut T, Coosemans W,
Decker G, et al. Prospective comparative study of integrated
positron emission tomography-computed tomography scan
compared with remediastinoscopy in the assessment of
residual mediastinal lymph node disease after induction
chemotherapy for mediastinoscopy-proven stage IIIA-N2
Non-small-cell lung cancer: a Leuven Lung Cancer Group
Study. J Clin Oncol 2006;24:3333-9.
18) Mateu-Navarro M, Rami-Porta R, Bastus-Piulats R, Cirera-
Nogueras L, González-Pont G. Remediastinoscopy after
induction chemotherapy in non-small cell lung cancer. Ann
Thorac Surg 2000;70:391-5.
19) Cerfolio RJ, Bryant AS. When is it best to repeat a 2-fluoro-
2-deoxy-D-glucose positron emission tomography/computed
tomography scan on patients with non-small cell lung cancer
who have received neoadjuvant chemoradiotherapy? Ann
Thorac Surg 2007;84:1092-7.
20) Chin R Jr, McCain TW, Lucia MA, Cappellari JO, Adair
NE, Lovato JF, et al. Transbronchial needle aspiration in
diagnosing and staging lung cancer: how many aspirates are
needed? Am J Respir Crit Care Med 2002;166:377-81.
21) Diacon AH, Schuurmans MM, Theron J, Brundyn K, Louw
M, Wright CA, et al. Transbronchial needle aspirates: how
many passes per target site? Eur Respir J 2007;29:112-6.
22) Stoll LM, Yung RC, Clark DP, Li QK. Cytology of
endobronchial ultrasound-guided transbronchial needle
aspiration versus conventional transbronchial needle
aspiration. Cancer Cytopathol 2010;118:278-86.