|Ahead of print publication
Performance characteristics of EUS-FNA biopsy for adrenal lesions: A meta-analysis
Suhag Patel1, Raxitkumar Jinjuvadia2, Anupama Devara3, Paul H Naylor4, Mohammad Anees5, Kartikkumar Jinjuvadia4, Mohammad Al-Haddad6
1 Division of Gastroenterology, Virginia Commonwealth University, Richmond, VA, USA
2 Division of Gastroenterology, Henry Ford Health System, Detroit, MI, USA
3 Department of Internal Medicine, Detroit Medical Center, Wayne State University, Detroit, MI, USA
4 Division of Gastroenterology, Detroit Medical Center, Wayne State University, Detroit, MI, USA
5 Division of Gastroenterology, Mayo Clinic, Rochester MN, USA
6 Indiana University School of Medicine, Indianapolis, IN, USA
|Date of Submission||26-Apr-2018|
|Date of Acceptance||03-Jul-2018|
|Date of Web Publication||12-Mar-2019|
Paul H Naylor,
Division of Gastroenterology, Detroit Medical Center, Wayne State University, 3990 John R Street, Detroit, MI 48201
Source of Support: None, Conflict of Interest: None
Background and Objective: The role of EUS-FNA biopsy (EUS-FNAB) for detection of metastatic lesions (mets) to adrenals has not been evaluated systematically. Our aim is to systematically evaluate the performance characteristics of EUS-FNAB in detecting metastasis to the adrenal glands. Materials and Methods: We performed a systematic search on PubMed and OvidSP from January 1990 to July 2016 using various search terms for EUS and adrenal lesion. Only articles published in English literature were included in the study. Studies with fewer than 10 patients were excluded from the study. Publication bias was assessed using Begg-Mazumdar test and visual inspection of funnel plots. Results: Eight studies including 360 adrenal lesions that underwent EUS-FNAB were identified. Of these, 137 FNABs were conclusive for malignancy. Sensitivity of EUS-FNAB in detecting metastasis to the adrenals was 95% (95% confidence interval [CI]: 90%–98%) and specificity was 99% (95% CI: 96%–100%). Pooled positivity of EUS-FNAB in detecting lung cancer metastasis to the adrenals was 44% (95% CI: 31.5%–57.3%). No evidence of publication bias was noted. Conclusion: Our study demonstrates that EUS-FNAB is highly sensitive and specific in detecting metastasis to adrenals. It also shows that up to about half of the patients with lung cancer and adrenal lesions on imaging have metastasis, a finding with profound implications on lung cancer staging and treatment.
Keywords: Adrenal mass, adrenal metastases in lung cancer, EUS-FNA biopsy
|How to cite this URL:|
Patel S, Jinjuvadia R, Devara A, Naylor PH, Anees M, Jinjuvadia K, Al-Haddad M. Performance characteristics of EUS-FNA biopsy for adrenal lesions: A meta-analysis. Endosc Ultrasound [Epub ahead of print] [cited 2019 May 23]. Available from: http://www.eusjournal.com/preprintarticle.asp?id=254008
| Introduction|| |
The increasing use of abdominal imaging in the form of an ultrasound (US), computed tomography (CT), magnetic resonance imaging (MRI), and other advanced techniques is resulting in incidental identification of adrenal lesions. While only 2% of all lesions are metastatic, this changes when imaging is done for cancer evaluation. Adrenal lesions identified during staging in patients with cancer can represent metastasis, in as many as 75% of patients. In lung cancer, adrenal metastases (mets) incidence ranging from 4.1% to 18% suggests that tissue verification is critical since metastatic involvement of the adrenals determines whether surgery or systemic therapies such as chemoradiation are the appropriate treatments.
Current imaging modalities lack the sensitivity and specificity to differentiate benign from malignant lesions, with 10% false-positive and false-negative rates being reported on CT scans., The positive predictive values (PPVs) of CT scan and fluorodeoxyglucose (FDG)-positron emission tomography (PET)-CT for adrenal mets can reach up to 62% and 81%, respectively,,, making tissue acquisition very important for tumor staging. Conventionally, CT-guided adrenal biopsy or laparoscopic/open adrenalectomies have been used; however, image-guided sampling techniques have their own limitations including high rates of nondiagnostic samples (up to 14%) and high complication rates (up to 12%).,
Endoscopic ultrasound-guided fine-needle aspiration biopsy (EUS-FNAB) is a promising alternative for sampling adrenal lesions due to its relative safety, accuracy, and high diagnostic yield., Few studies have attempted to evaluate the safety and diagnostic yield of EUS-FNAB for adrenal lesions, and most were limited by small sample size. In the current meta-analysis, we aim to study the performance characteristics of EUS-FNAB of adrenal lesions in identifying the metastasis in patients with nonadrenal malignancies.
| Materials and Methods|| |
Study selection/search strategy
We performed a comprehensive systematic literature search in PubMed and OvidSP to identify peer-reviewed articles that evaluated the performance of EUS-FNAB in detecting mets to adrenals. Search period was set from January 1990 to July 2016 without language restriction using the following terms: EUS, EUS-FNAB, Endosonography, Endoscopic ultrasound AND adrenal lesion, adrenal mass, adrenal tumor, and adrenal metastasis. Crosschecking was performed through the reference list of each included study to identify further relevant studies. The process of systematic review was conducted in adherence to standards of quality for reporting meta-analysis. Two reviewers (SP and AD) independently and thoroughly assessed all the articles per predefined inclusion and exclusion criteria. Any disagreements over study selection were resolved by consulting with a third reviewer (KJ).
Relevant studies were only included if they met the following criteria: (1) age of study participants >18 years and (2) original article published in English. Exclusion criteria set for the study: (1) Studies where <10 EUS-FNABs were reported. This was done to avoid selection bias for studies with few patients. (2) Case reports. (3) Abstracts.
Reference standard for verification of biopsy observations
Various studies used variable criteria for establishing the final pathological diagnosis of adrenal lesions. These included surgical resection, death from progression of disease, repeat radiological imaging, and clinical follow-up. Studies relying on prolonged clinical follow-up considered patient longevity at 6–24 months as proof of benignancy of adrenal lesion since adrenal mets are often associated with poor survival.
After careful review of each study, the following data were extracted: publication data (including first author's last name and first initial, year of publication, and country of origin), sample size, demographics of participants, type of study, primary source of malignancy, laterality of adrenal involvement (right or left or both), prior imaging workup, follow-up duration, and availability of a conclusive pathology source.
Assessment of methodological quality
At present, there are no defined criteria to evaluate the quality of studies without a control arm. We used Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2) criteria to evaluate the quality of included studies.
We calculated pooled sensitivity, specificity, likelihood ratios (LRs), and odds ratio to assess the performance of EUS-FNA in identifying metastatic lesions to adrenal glands. Pooling was performed using the random-effects model. We also constructed forest plots to compare the point estimates of each individual study with pooled summary results. Weight of each study is depicted by the width of point estimates in the forest plots. We used Chi-square, I2, and Cochran's Q test to assess heterogeneity. We also prepared a plot representing area under receiver operating characteristic (ROC) curve to summarize the evidence. The closer the ROC curve was to 1, the higher the diagnostic accuracy of a test was.
For the final analysis, only those studies that provided sufficient data for construction of 2 × 2 contingency tables were considered. Publication bias was assessed using the Begg-Mazumdar test. We used Meta-Disc version 1.4 (Unit of Clinical Biostatistics, Ramon y Cajal Hospital, Madrid, Spain) to calculate pooled sensitivity, specificity, positive LR, negative LR, and the summary ROC curve. We used comprehensive meta-analysis version 3.0 (Biostat, Englewood, New Jersey, USA) to calculate pooled positivity of EUS-FNAB in detecting lung cancer metastasis to adrenals and pooled technical success rates of EUS-FNAB. Since this study does not compare the outcomes of two different tests, we have not reported P values for summary effects.
In a meta-analysis, individual studies can disproportionately influence the results if they incur undue weight. To avoid this bias, we performed sensitivity analysis by removing each individual study data from the pooled results one at a time and evaluated the summary outcomes for the remaining studies to assess if that led to any major change in outcomes.
| Results|| |
A total of 126 titles were identified after an initial literature search that matched our predefined criteria. After careful review, we excluded 101 titles and selected 25 relevant titles for full article review. After excluding further irrelevant studies, eight studies were selected for the current analysis. [Figure 1] demonstrates the study selection algorithm. Characteristics of each of these included studies are shown in [Table 1], and individual study data including sample size, number of EUS-FNAB examinations in each, patients with known or suspected malignancy, number of positive EUS-FNABs, EUS-FNAB conclusive for lung cancer metastasis, methods of follow-up after EUS-FNAB, and adverse events associated with FNAB, if any, are presented in [Table 2].
QUADAS-2 criteria were used to assess the quality of studies included, as summarized in [Figure 2]. In most of the studies, the risk of selection bias was low. There were no applicability concerns regarding patient selection. There was no risk of bias regarding index test or its applicability. However, studies where only clinical follow-up was used as reference standard raised concerns about risk of bias and its applicability. Based on the above, eight studies were included in the analysis,,,,,,, of technical success rate in acquiring a diagnostic sample with EUS-FNAB [Figure 3]. While analyzing the performance characteristics of EUS-FNAB, two studies, were excluded: the first by Stelow et al. where no follow-up data after EUS-FNAB were provided and the second by Bodtger et al. where clinical follow-up and longevity at 2 years were considered signs of benignancy of a lesion.
|Figure 2: Quality of eligible studies as assessed by the QUADAS-2 criteria|
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|Figure 3: Forest plot of studies reporting outcomes of EUS-FNAB in detecting metastases to adrenals: Pooled sensitivity|
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A total of 360 EUS-FNABs of adrenal glands were performed in the 8 studies included. Of these, 322 (89%) had suspected or known malignancy elsewhere. One of the selected studies was multicenter and three were prospective.,, Two of the studies only sampled the left adrenal gland, while the rest sampled either the right or the left. On-site cytopathology was available in most studies except two,, while one study did not report this data. Included studies used various available needles for obtaining the sample. Four studies,,, used 22 gauge, one study used 19 gauge, while one study did not report on needle size. Stelow et al. used either 22- or 25-gauge needles while Martinez et al. used 19-, 22-, or 25-gauge needles.
Among 322 patients with suspected or known malignancy anywhere, 137 had malignant cytology on EUS-FNAB of an adrenal lesion. Similarly, among 221 patients with suspected or known lung cancer, 108 had malignant cytology on EUS-FNAB of an adrenal lesion; however, the study by Stelow et al. was excluded from this calculation as required details were not provided by the authors. The pooled sensitivity and specificity of EUS-FNAB in detecting metastasis to the adrenals were 95% (95% confidence interval [CI]: 90%–98%) and 99% (95% CI: 96%–100%), respectively [Figure 4] and [Figure 5]. The pooled positive LR (+LR) was 29.60 (95% CI: 10.57–82.90) and pooled negative LR (−LR) was 0.08 (95% CI: 0.04–0.16). An ROC curve is shown in [Figure 6]. The overall pooled technical success rate in obtaining diagnostic tissue was 94% (95% CI: 90%–96%) [Figure 3]. The pooled positivity in identifying lung cancer metastasis to the adrenals was 44% (95% CI: 31.5%–57.3%) [Figure 7].
|Figure 4: Forest plot of studies reporting outcomes of EUS-FNAB in detecting metastases to adrenals: Pooled specificity|
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|Figure 7: Pooled positivity in detecting lung cancer metastases to adrenals|
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To ascertain that no one study incurred undue weight leading to profound impact on the results of the analysis, we performed sensitivity analysis by removing one study at a time from cumulative analysis and recalculating performance characteristics. We concluded that no one study had enough weight to alter the results of the analysis.
| Discussion|| |
To our knowledge, this is the first meta-analysis on the diagnostic yield and performance characteristics of EUS-FNAB of adrenal glands. Our meta-analysis clearly demonstrates that EUS-FNAB of the adrenal glands is highly sensitive (pooled sensitivity 95% with 95% CI: 90%–98%) and specific (pooled specificity 99% with 95% CI: 96%–100%) at diagnosing malignant lesions which is superior to other imaging-guided sampling techniques.,,,, In addition, pooled negative LR of 0.08 indicates that it can be used as a single test alone to exclude malignancy from adrenal lesions noted on prior imaging workup. If EUS-FNAB is negative for malignancy, patients can probably be followed clinically without requiring any further invasive workup. In addition, EUS-FNAB is highly accurate at differentiating malignant lesions from benign ones as shown in [Figure 6].
Furthermore, EUS is more effective at obtaining diagnostic samples compared to other modalities. As demonstrated in [Figure 3], the pooled technical success rate of EUS for obtaining diagnostic sample from adrenal lesion is about 94% (95% CI: 90%–96%). This is likely due to the fact that the left adrenal gland lies in close proximity to the stomach and is easily accessible through a transgastric approach. In general, visualizing the right adrenal gland can more difficult compared to left, as it requires duodenal maneuvering of the EUS scope. In a retrospective study by Uemura et al., visualization of the right adrenal gland was attempted in 150 patients with potentially resectable lung cancer and was feasible in 131 of 150 patients (87.3%). Subgroup analysis including studies that sampled the right adrenal gland in the current meta-analysis showed 100% diagnostic yield; however, the sample size was very small [Table 2].
Since the adrenal gland is a site of predilection for lung cancer metastasis, EUS-FNAB can be particularly useful in evaluating suspected metastatic adrenal lesions in patients with known or suspected lung cancer. As shown in [Figure 7], the pooled sensitivity of EUS-FNAB from an adrenal lesion was about 44% (95% CI: 31.5%–57.3%) in patients with known or suspected lung cancer. This demonstrates that about half of the patients with known or suspected lung cancer presenting with an adrenal lesion have metastatic disease, making it unresectable Stage 4 disease. Confirming adrenal metastatic disease in lung cancer profoundly impacts subsequent management decisions and practically excludes surgery in this case. The study by Bodtger et al. specifically evaluated the impact of EUS-FNAB on the clinical decision-making in such patients. There were forty patients with known or suspected lung cancer in whom the impact of EUS on the overall treatment plan was assessed. In this study, the authors identified left adrenal metastasis by EUS-FNAB in two out of four patients who had a normal left adrenal gland reported on prior CT scan. Thus, EUS-FNAB avoided futile surgery in these two patients who were upstaged to Stage IV disease. On the other hand, 28% (10 out of 36) became surgical candidates because of negative EUS-FNAB of a left adrenal lesion in whom prior CT scan was abnormal. In a subsequent study, Eloubeidi et al. evaluated 59 consecutive patients, where EUS-FNAB confirmed malignancy in 22. The same study assessed the correlation between size of the adrenal lesion and likelihood of malignancy. Although the malignant lesions were more likely to be larger (3.1 cm) compared to benign lesions (2.3 cm), EUS imaging had an accuracy of 68% for differentiating malignant from benign lesions based on a size threshold of 3 cm. Therefore, size alone is not reliable for differentiating malignant from benign lesions, and tissue acquisition is still needed. The importance of EUS-guided tissue acquisition is further emphasized by the fact that imaging characteristics alone are unreliable in differentiating malignant from benign lesions. Porte et al. reported a false-positive rate of malignancy of 21% and false-negative rate of 11% by CT scan based on imaging characteristics only. Another study showed the false-positive rate to be as high as 67% with MRI.
With improving technology, FDG-PET or FDG-PET/CT may seem like a reliable noninvasive option for evaluating adrenal lesions. A study by Schuurbiers et al. evaluated the correlation between FDG-PET results and EUS-FNAB outcomes. The study included 46 patients referred for EUS-FNAB due to positive FDG-PET scan. In 32 of 46 patients (70%), EUS-FNAB confirmed malignancy. Considering a cytologically conclusive EUS-FNAB as the reference standard, FDG-PET had a PPV of 74%. A study by Erasmus et al. showed FDG-PET specificity of 80% at detecting malignancy in patients with lung cancer and adrenal lesions. Finally, a review by Stone et al. showed that the FDG-PET/CT had a high sensitivity of 94%, but due to specificity being <90%, tissue acquisition for confirmation of malignancy is recommended.
In addition to its very high diagnostic accuracy, EUS-FNAB offers a safe alternative to image-guided sampling and is associated with fewer adverse events. Since the left adrenal gland is easily accessible through a transgastric approach with no intervening organs, the likelihood of adverse events remains very low. In comparison, a percutaneous approach can be associated with up to 12% adverse events including hemorrhage, pneumothorax, pain, pancreatitis, and rarely, needle track seeding, with hemorrhage and pneumothorax being the most common ones. No major EUS-FNAB-related adverse events were reported in any of the studies included in this meta-analysis. EUS also offers other advantages such as the lack of radiation exposure, elimination of contrast administration, needle insertion under real-time US guidance, and the ability to perform sampling during the same EUS session when a lesion is detected.
One important consideration not to be ignored is the potential to be sampling a pheochromocytoma. Typically, these patients have no extra-adrenal malignancy on imaging and more typically present with hypertension, palpitations, sweating, and anxiety episodes. Therefore, if an adrenal lesion is identified without concerns for extra-adrenal malignancy, appropriate workup should be performed to rule out possibility of pheochromocytoma before sampling any adrenal lesion. In a case series of four patients (with unsuspected pheochromocytoma) who underwent percutaneous biopsies of the adrenal gland, one patient experienced alteration in blood pressure during procedure while another developed severe hypertensive crisis during percutaneous sampling. Case reports of hypertensive crisis after EUS-FNAB of adrenal lesion in patients with lung cancer have been published. Using a smaller size needle (25 gauge, for example), limiting the number of passes and employing onsite cytopathology review can minimize trauma to a potential pheochromocytoma.
Our meta-analysis has some limitations. The most important one being the unavailability of surgical specimen for a final pathologic diagnosis in many of the studies included. In almost all studies, biopsies confirmatory of malignancy were treated as “definitive evidence of malignancy,” and hence, no surgical management was offered. This is consistent with most EUS literature, where a confirmatory cytology is treated as a reference standard for malignancy. Moreover, these patients were noted to have poor outcomes on follow-up which further supports the FNAB diagnosis. It should be noted also that there was no surgical pathology confirmation of benign lesions which could have introduced bias by considering all those biopsies as true negatives and missing some false negatives. In our analyses, we only included patients for whom appropriate follow-up information was available. The lack of uniformity between these studies in terms of follow-up duration and methods is another limitation worthy of mention.
| Conclusion|| |
In summary, our meta-analysis demonstrates that the EUS-FNAB is highly sensitive and specific for diagnosing malignant adrenal lesions and is extremely accurate at differentiating malignant from benign lesions. We strongly recommend performing EUS-FNAB in patients with known or suspected lung cancer and imaging evidence of an adrenal lesion since only half of these patients have adrenal metastasis. This information can be a key determinant with respect to surgical treatment or chemotherapy focused on the treatment of metastatic disease.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Martinez M, LeBlanc J, Al-Haddad M, et al
. Role of endoscopic ultrasound fine-needle aspiration evaluating adrenal gland enlargement or mass. World J Nephrol
Grumbach MM, Biller BM, Braunstein GD, et al
. Management of the clinically inapparent adrenal mass (“incidentaloma”). Ann Intern Med
Chapman GS, Kumar D, Redmond J 3rd
, et al
. Upper abdominal computerized tomography scanning in staging non-small cell lung carcinoma. Cancer
Bodtger U, Vilmann P, Clementsen P, et al
. Clinical impact of endoscopic ultrasound-fine needle aspiration of left adrenal masses in established or suspected lung cancer. J Thorac Oncol
Silvestri GA, Tanoue LT, Margolis ML, et al
. The noninvasive staging of non-small cell lung cancer: The guidelines. Chest
Okada M, Shimono T, Komeya Y, et al
. Adrenal masses: The value of additional fluorodeoxyglucose-positron emission tomography/computed tomography (FDG-PET/CT) in differentiating between benign and malignant lesions. Ann Nucl Med
Schuurbiers OC, Tournoy KG, Schoppers HJ, et al
. EUS-FNA for the detection of left adrenal metastasis in patients with lung cancer. Lung Cancer
Sung YM, Lee KS, Kim BT, et al
. (18)F-FDG PET versus (18) F-FDG PET/CT for adrenal gland lesion characterization: A comparison of diagnostic efficacy in lung cancer patients. Korean J Radiol
Porte HL, Ernst OJ, Delebecq T, et al
. Is computed tomography guided biopsy still necessary for the diagnosis of adrenal masses in patients with resectable non-small-cell lung cancer? Eur J Cardiothorac Surg
Lumachi F, Borsato S, Brandes AA, et al
. Fine-needle aspiration cytology of adrenal masses in noncancer patients: Clinicoradiologic and histologic correlations in functioning and nonfunctioning tumors. Cancer
DeWitt J, Alsatie M, LeBlanc J, et al
. Endoscopic ultrasound-guided fine-needle aspiration of left adrenal gland masses. Endoscopy
Eloubeidi MA, Black KR, Tamhane A, et al
. A large single-center experience of EUS-guided FNA of the left and right adrenal glands: Diagnostic utility and impact on patient management. Gastrointest Endosc
Moher D, Shamseer L, Clarke M, et al
. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Syst Rev
Eloubeidi MA, Seewald S, Tamhane A, et al
. EUS-guided FNA of the left adrenal gland in patients with thoracic or GI malignancies. Gastrointest Endosc
Thompson SG, Higgins JP. How should meta-regression analyses be undertaken and interpreted? Stat Med
Whiting PF, Rutjes AW, Westwood ME, et al
. QUADAS-2: A revised tool for the quality assessment of diagnostic accuracy studies. Ann Intern Med
Begg CB, Mazumdar M. Operating characteristics of a rank correlation test for publication bias. Biometrics
Jhala NC, Jhala D, Eloubeidi MA, et al
. Endoscopic ultrasound-guided fine-needle aspiration biopsy of the adrenal glands: Analysis of 24 patients. Cancer
Puri R, Thandassery RB, Choudhary NS, et al
. Endoscopic ultrasound-guided fine-needle aspiration of the adrenal glands: Analysis of 21 patients. Clin Endosc
Stelow EB, Debol SM, Stanley MW, et al
. Sampling of the adrenal glands by endoscopic ultrasound-guided fine-needle aspiration. Diagn Cytopathol
Uemura S, Yasuda I, Kato T, et al
. Preoperative routine evaluation of bilateral adrenal glands by endoscopic ultrasound and fine-needle aspiration in patients with potentially resectable lung cancer. Endoscopy
Burt M, Heelan RT, Coit D, et al
. Prospective evaluation of unilateral adrenal masses in patients with operable non-small-cell lung cancer. Impact of magnetic resonance imaging. J Thorac Cardiovasc Surg
Erasmus JJ, Patz EF Jr., McAdams HP, et al
. Evaluation of adrenal masses in patients with bronchogenic carcinoma using 18F-fluorodeoxyglucose positron emission tomography. AJR Am J Roentgenol
Stone WZ, Wymer DC, Canales BK. Fluorodeoxyglucose-positron-emission tomography/computed tomography imaging for adrenal masses in patients with lung cancer: Review and diagnostic algorithm. J Endourol
Tsitouridis I, Michaelides M, Stratilati S, et al
. CT guided percutaneous adrenal biopsy for lesions with equivocal findings in chemical shift MR imaging. Hippokratia
Sharma KV, Venkatesan AM, Swerdlow D, et al
. Image-guided adrenal and renal biopsy. Tech Vasc Interv Radiol
Casola G, Nicolet V, vanSonnenberg E, et al
. Unsuspected pheochromocytoma: Risk of blood-pressure alterations during percutaneous adrenal biopsy. Radiology
de Vries AC, Poley JW. Hypertensive crisis after endoscopic ultrasound-guided fine-needle aspiration of the right adrenal gland. Endoscopy
2014;46 Suppl 1 UCTN: E447-8.
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7]
[Table 1], [Table 2]