Endoscopic Ultrasound Fine-Needle Biopsy May Contribute to the Diagnosis of Malignant Lymph Nodes

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Clin Endosc. 2020;53(5):508-509
Publication date (electronic) : 2020 September 24
doi : https://doi.org/10.5946/ce.2020.199
Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan
Correspondence: Mamoru Takenaka Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama 589-8511, Japan Tel: +81-72-366-0221, Fax: +81-72-367-2880, E-mail: mamoxyo45@gmail.com
Received 2020 July 24; Revised 2020 July 24; Accepted 2020 July 31.

See “Endoscopic Ultrasound Fine-Needle Aspiration versus Fine-Needle Biopsy for Lymph Node Diagnosis: A Large Multicenter Comparative Analysis” by Diogo Turiani Hourneaux de Moura, Thomas R. McCarty, Pichamol Jirapinyo, et al., on page [Related article:] 600-610.

We would like to comment on a multicenter retrospective study of prospectively collected data for evaluating the outcomes of endoscopic ultrasound fine-needle aspiration (EUS-FNA) and endoscopic ultrasound fine-needle biopsy (EUS-FNB) for lymph node (LN) sampling authored by de Moura et al. [1].

The treatment strategy and disease prognosis are markedly affected by whether lymphadenopathy is malignant or benign. EUS and EUS-guided sampling are well-known as suitable examination methods for assessing lymphadenopathy. EUS provides a good image of the affected LNs from the lumen of the gastrointestinal tract and allows for tissue sampling using these images for “guidance”. EUS-guided sampling has now become the standard of care for close examination of lymphadenopathy [2]. EUS-FNA is typically performed as EUS-guided sampling, which can provide the LN tissue for cytological evaluation. Since its development, the device has been developed and ingestion about sampling method have been devised to improve the diagnostic efficacy. However, the reported sensitivity and specificity of EUS-FNA (88% and 96.4%, respectively) are less than the ideal values [3].

Recently, EUS-FNB has been developed as a further development of the EUS-FNA technique. With EUS-FNB, a larger amount of tissue can be sampled compared to that with EUS-FNA; this is expected to contribute towards the increase in the efficacy of diagnosing the affected tissue. The usefulness of FNB for subepithelial lesions, pancreatic neuroendocrine tumors, and pancreatic cancer has already been reported [4,5]. Furthermore, the usefulness of EUS-FNB has also been reported with respect to molecular yields for genomic analysis [5,6]. In contrast, a comparative study of FNA and FNB for the diagnosis of malignant LNs has not been performed.

When evaluating EUS-FNA or EUS-FNB for the diagnosis of malignant LNs, securing cases with surgical specimens, which are required for pathological analysis, has become difficult, as many cases with malignant LNs are not indicated for surgical resection. Many studies evaluating the LNs have limited their focus to surgical cases [7,8].

In addition, in many cases, there was a problem with multiple LNs. In these cases, the EUS-FNA results were markedly affected by the lesion targeted for tissue sampling. The usefulness of contrast-enhanced EUS has also been reported, but the identification of appropriate puncture lesions is still challenging [9]. Moreover, it is very difficult to distinguish between the LNs for which FNA was performed and the resected lesions, even if surgical resection was performed.

In the current issue, the authors performed a multicenter retrospective study to compare the diagnostic efficacy of EUS-FNA and EUS-FNB. Postoperative anatomopathological analysis was used as the gold standard for examination in some cases. However, as noted by the authors, the gold standard was not the pathological examination of the surgically resected specimens but the patient status after 6 months in many cases. This observation suggests that in many cases, the preoperative and postoperative pathological results were not corroborated on the basis of the specimen pathology. The results of this study should be interpreted with due recognition of this limitation.

In this study, 209 patients underwent EUS-guided LN sampling at five hospitals. The mean lesion size was 16.22±8.03 mm, with similar sensitivity and accuracy between FNA and FNB (sensitivity: 67.2% vs. 75.0%, p=0.216 and accuracy: 78.8% vs. 83.2%, p=0.423). The specificity of FNB was better than that of FNA (100.0% vs. 93.6%, p=0.01) [1]. Although significant differences were not observed in the diagnostic yields, it was suggested that FNB may have a better clinical effect than FNA.

In addition, the study also included location-specific LN analysis. FNB showed higher sensitivity (FNB vs. FNA: 81.1% vs. 64.7%, p=0.031 and 80.9% vs. 58.3%, p=0.023) and accuracy (FNB vs. FNA: 88.1% vs. 75.3%, p=0.053 and 88.9% vs. 70.5%, p=0.038) for the abdominal and peri-hepatic LNs, respectively [1]. These results provide very useful information for daily clinical practice.

The highlight of this paper is that even in situations where rapid on-site evaluation (ROSE) is not possible, a significant difference may not be noted between the diagnostic yield of FNB alone and FNA with ROSE. ROSE allows for earlier diagnosis and a decrease in the number of punctures, and in combination with the large amount of tissue volume obtained with EUS-FNB, it is clearly very useful [10]. However, ROSE should ideally be performed by a pathologist (although it can also be performed by an endoscopist) and this may not be possible in all institutions.

In the present study, the sampling methods with or without ROSE were also compared. ROSE with FNA showed a higher sensitivity than FNA alone (97.7% vs. 63.5%, p=0.004). No statistically significant difference was observed between the accuracy of FNA+ROSE and the accuracy of FNB alone (94.4% vs. 80.7%, p=0.161) [1].

Although this result should be interpreted with caution, especially since only 17.2% of the study population underwent additional testing with ROSE according to the author, the results largely support the useful contribution of EUS-FNB in clinical practice [1].

The authors noted several limitations of their study, including the study design (retrospective design and lack of randomization), selection bias, including different needle sizes, and the possibility that patients were lost to follow-up. However, despite these limitations, this study might shed more light on the difficulties encountered when diagnosing the LNs in clinical practice because this study was the largest multicenter study that specifically compared the effectiveness and safety of EUS-FNA and EUS-FNB for LN sampling.

To confirm the validity of EUS-FNB for LN sampling, further prospective studies including more cases with histopathological answer with surgical specimens under the standardization of needles and ROSE condition are recommended.


Conflicts of Interest: The authors have no financial conflicts of interest.


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