Endoscopic ultrasonography: an advancing option with duality in both diagnosis and treatment of gastrointestinal oncology

Department of Gastroenterology, Union Hospital of Fujian Medical University, Fuzhou 350001, China

Correspondence to: Dr. Fenglin Chen. Department of Gastroenterology, Union Hospital of Fujian Medical University, 29 Xinquan Road, Fuzhou 350001, China. Email: drchenf@163.com.

Endoscopic ultrasonography: an advancing option with duality in both diagnosis and treatment of gastrointestinal oncology

Fenglin Chen

Department of Gastroenterology, Union Hospital of Fujian Medical University, Fuzhou 350001, China

Correspondence to: Dr. Fenglin Chen. Department of Gastroenterology, Union Hospital of Fujian Medical University, 29 Xinquan Road, Fuzhou 350001, China. Email: drchenf@163.com.

Since their introduction into the clinical practices in 1980s, techniques of endoscopic ultrasonography (EUS) have been rapidly developing and are now in widespread use in gastrointestinal oncology. Evolving from the classical option, EUS today has been much innovated with addition of a variety of novel ideation which makes it a powerful tool with encouraging duality for both diagnostic and therapeutic purposes. There is a dire need for physicians in this feld to understand the status quo of EUS as related to the management and detection of gastrointestinal tumors, which is globally reviewed in this paper.

Gastrointestinal tract; oncology; ultrasonography; endoscopic; treatment

View this article at:http://dx.doi.org/10.3978/j.issn.1000-9604.2014.12.14

Introduction

Since its introduction in the 1980s and, particularly beginning from this millennium, the rapidly developing endoscopic ultrasonography (EUS) has found its widespread use in clinical practice and played an important role in the diagnosis and treatment for tumors (1-5) in many disciplines, such as gastrointestinal oncology. Here we present a review on the advances of EUS in this feld.

Endoscopic ultrasonography (EUS) as a diagnostic tool

EUS, a major diagnostic procedure for gastrointestinal submucosal tumors (SMTs) which not only clearly shows tumor location, size, margin, echo and originating layers (6) but also effectively identifes different tumors, is currently considered as the most accurate procedure for detecting and making diagnosis of SMTs for its high sensitivity and specifcity (7-11).

EUS-guided fine needle aspiration biopsy (EUS-FNA) is a mature minimally invasive procedure in identifying and staging the diseases in the gastrointestinal tract and adjacent tissues or organs for its advantage in short puncture distance and good safety (12,13). EUS-FNA, though more often used in the biopsy of pancreas and lymph nodes, is also widely used in diagnosing various lesions including SMTs, applied in tissues and organs including intraperitoneal and mediastinal lymph nodes, pancreas, adrenal gland, gallbladder, bile ducts, liver, lung, kidney and rectum (14-16). It has been confrmed that EUS-FNA signifcantly improves the diagnostic accuracy with sensitivity of 80-85% and specificity of nearly 100% (17-19). According to recent studies, optical biopsy can be performed by penetrating a needle-like confocal laser endomicroscopic probe into pancreatic cystic lesions with puncture needle guided by EUS (20-23), which assists the evaluation of lesions but the sensitivity and accuracy is still to be confirmed by further study. Moreover, EUS-FNA is helpful in exploring the molecular pathogenesis of pancreatic cancer. EUS-FNA is used to obtain pancreatic tissues not only for molecular study and polymerase chain reaction (PCR) analysis, but also for DNA analysis to identify benign and malignant neoplasms, and for gene expression profile analysis in advanced pancreatic ductal adenocarcinoma (24-27). Suspected pancreatic ductal adenocarcinoma that cannot be determined by EUS-FNA may be subject to KRAS mutation analysis of the biopsy tissues (28,29). There arealso studies on the diagnostic value of mucin (MUC1, MUC2 and MUC5AC) expression in biopsy tissues obtained from pancreas (30).

However, manipulation of EUS-FNA can be difficult and require skillful technique and the sensitivity and the negative predictive value of EUS-FNA for pancreatic tumor and other lesions is still insufficient. Meanwhile, as an invasive examination, EUS-FNA may cause complications including bleeding, infection and tumor rupture (31,32). In addition, some patients are not suitable candidates for EUSFNA and/or unwilling to undergo EUS-FNA. Therefore, new techniques such as elastography, contrast-enhanced EUS (CE-EUS) are introduced clinically to improve the accuracy of EUS in differentiating the malignancy of lesions in recent years (33).

EUS elastography is a non-invasive procedure that has been used to evaluate the elasticity coefficient (firmness) and differentiate the malignancy of lesions besides obtain conventional ultrasound images (34). Giovannini et al. frstly reported the diagnostic value of EUS elastography in pancreatic masses and lymph nodes in 2006 (35) and proved that EUS elastography is superior to conventional EUS in its accuracy, sensitivity and specificity for differentiating the malignance of pancreatic masses and lymph nodes in a multi-center clinical study completed in 2009 (36). In an European multi-center study on computer-assisted quantitative analysis of continuous and dynamic EUS elastographic images carried out by S?ftoiu et al., the accuracy, sensitivity, specificity, positive predictive value and negative predictive values of EUS elastography on the malignancy of space-occupying pancreatic lesions are 85.4%, 93.4%, 66.0%, 92.5% and 68.9%, respectively (37). The sensitivity and specificity of EUS elastography on lymph nodes are 91.1% and 60.0%, respectively, as reported by Sun et al. (38). Clinicians are often unable to specifcally determine the nature of the lesions only based on EUS and elastographic images since the judgment is highly subjective and no consensus on the evaluation criteria has been reached yet in spite of the comparatively high accuracy of EUS elastography in identifying the malignancy of lesions. Nevertheless, EUS elastography is important in those unable to undergo EUS-FNA or the suspicious cases with repeated negative results in EUS-FNA. EUS elastography in identifying the malignancy of lymph nodes and pancreatic space-occupying lesion has been reported, still researches on its diagnostic value for other gastrointestinal spaceoccupying lesions are yet to be made (39). There might be more indications for EUS elastography after further study in the near future, including differentiating the malignancy of solid hepatic space-occupying lesions (40,41), assessing the invasion of esophageal and gastric cancer to adjacent organs and evaluating the solid adrenal lesions on the left by distinguishing adenomas from metastases (42).

CE-EUS (43), an imaging procedure that generates high resolution images of tissues in the body using ultrasound contrast agent, is now applied in the detection of solid tumors of the pancreas (cancers, neuroendocrine tumors), pancreatic cystic tumors (mucinous cystadenoma, intraductal papillary mucinous tumors), pancreatic pseudocyst, pancreatitis, and extrahepatic bile duct cancer (44,45), for identification of gastrointestinal stromal tumors, smooth muscle tumors (46) and adrenal tumors (47,48), and for differentiation of the malignancy of lymph nodes (49). Differences are noted in the enhancement mode, time-phase characteristics and classification of enhanced intensity between normal tissues and lesions. CE-EUS is demonstrated to be superior to multi-slice spiral CT for diagnosis of pancreatic mass of less than 2 cm and the diagnostic value of EUS-FNA is significantly improved when used in combination with CE-EUS (50).

EUS for therapeutic purposes

In recent years, studies on EUS in treatment for cancer are booming along with wide recognition of various emerging techniques. Interventional EUS therapy might not significantly improve the survival in malignant cases, but rather, it relieves pain, induces tumor cell necrosis and improves life quality.

EUS-guided celiac plexus neurolysis (EUS-CPN) is generally considered safe but it does not allow direct injection into celiac ganglia. According to Levy et al., 94% cancer patients achieved pain relief after EUS-guided celiac ganglia neurolysis (EUS-CGN), which initially implicates the safety of EUS-CGN and EUS-CPN (51). Ascunce et al. (52) and Sakamoto et al. (53) presented the safety and effcacy of EUS-CGN as well. Besides, Sakamoto et al. referred to EUS-guided broad plexus neurolysis (EUSBPN) but did not give defnite conclusion on its effcacy and safety. For EUS-CGN, no serious complications have been reported yet (54), however its effcacy and safety remains to be confrmed by in-depth research and large-sample clinical trials.

The development of interventional EUS techniques enables advanced pancreatic cancer patients undergo radioactive and chemotherapeutic seed implantationvia EUS-guided fine-needle injection (EUS-FNI). Sun et al. firstly conducted EUS-guided iodine-125 seed implantation for pancreatic cancer in pig models in 2005 and no signifcant complications were noted (55), and then further clinical trials were performed in 2006 (56). Jin et al. (57) further evaluated the clinical effcacy and safety of EUS-guided iodine-125 radioactive seed implantation combined with gemcitabine for advanced pancreatic cancer. Nevertheless, studies on how to uniformly distribute seeds, the dosage control of radioactive seeds, and displacement of seeds after implantation are still to be made in EUS-guided radioactive seed implantation.

Image-guided radiation therapy (IGRT) guarantees for the accuracy and less complications of radiotherapy by real-time monitoring tumor or its markers by integrating radiation therapy machine with imaging equipment. In recent years, some scholars are trying to combine EUS techniques with IGRT along with the rapid development of EUS techniques. Park et al. treated advanced pancreatic cancer patients with IGRT by implanting gold fiducial markers with 19G needle guided by EUS and achieved a success rate of 88 % (58). In a retrospective study carried out by DiMaio et al., 30 cases with mediastinal and upper gastrointestinal cancer underwent EUS-guided IGRT, 97% of which achieved EUS-guided implantation of more flexible gold coil as reference marker using 22G needle without intraoperative complications (59). Both studies demonstrated the feasibility of EUS-guided gold fiducial placement for IGRT.

EUS-guided radiofrequency ablation (EUS-RFA) (60-62) and laser ablation (63) may shrink the tumor to some extent, but still clinical studies are to be performed to support its feasibility and safety.

EUS-guided biliary drainage has recently emerged as an effective procedure that utilizes EUS-guided puncture needle into the bile duct through gastric and duodenal wall, followed by insertion of guide wire along the needle, expansion and placement of drainage stent, thereby to establish internal drainage of biliary pathways to relieve bile duct obstruction. It is especially suitable for obstructive jaundice cases after failed ERCP regardless of its causes (64,65). Giovannini et al. (66) reported the first EUS-guided biliary and duodenal drainage in a patient with pancreatic cancer, and firstly performed EUS-guided hepaticogastrostomy (EUS-HGS) in a patient with proximal metastatic biliary obstruction in 2003 (67). Yamao et al. (68) reported cholecystoduodenostomy followed by biliary drainage in five cases, and they suggested that the procedure was more easily performed through duodenal bulb because of shorter puncture path into the extrahepatic bile duct, being free from vascular interference and puncture towards the hepatic portal; the drainage was carried out away from site of tumor obstruction; EUS-guided procedures were safer; and the dilated puncture channel enables large enough fistula to allow placement of 8.5 Fr bracket. In studies carried out by Artifon et al., there were no significant differences in the success rate, complications, cost of treatment and quality of life in malignant distal biliary obstruction patients who underwent EUS-guided choledochoduodenostomy and those who underwent percutaneous transhepatic biliary drainage (PTBD); for patients with distal bile duct cancer, no significant difference in technique and clinical outcomes was noted between the EUS-CD patient group and the surgery group, but there was only one case of self-limiting bleeding occurred in EUS-CD group and the cost of EUSCD group was significantly lower than the surgery group (69). EUS-CD is a potentially effective non-surgical biliary drainage procedure in advanced malignant distal bile duct obstruction, in spite of the diffculties in operating EUS-CD and the lack of prospective and multi-center trials with large-sample size.

As the equipment and technique develop, EUS will offer much clearer images with more comprehensive functions, and it will be undoubtedly more and more applied in diagnosis and treatment of cancer with a promising future.

Acknowledgements

Funding: This study was sponsored by the Key Clinical Specialty Discipline Construction Program of Fujian, P.R.C and the Special Funds of Finance Department of Fujian Province (2012B013).

Disclosure: The author declares no confict of interest.

1. De Angelis C, Brizzi RF, Pellicano R. Endoscopic ultrasonography for pancreatic cancer: current and future perspectives. J Gastrointest Oncol 2013;4:220-30.

2. Bu Z, Ji J. Controversies in the diagnosis and management of early gastric cancer. Chin J Cancer Res 2013;25:263-6.

3. Gill KR, Wallace MB. Endoscopic ultrasound and staging of non-small cell lung cancer. Minerva Med 2007;98:323-30.

4. Ye X, Yu JC, Kang WM, et al. Totally laparoscopicdistal gastrectomy reconstructed by Roux-en-Y with D2 lymphadenectomy and needle catheter jejunostomy for gastric cancer. Transl Gastrointest Cancer 2013;2:21-5.

5. Miyaaki H, Ichikawa T, Taura N, et al. Endoscopic management of esophagogastric varices in Japan. Ann Transl Med 2014;2:42.

6. Guo J, Liu Z, Sun S, et al. Endosonography-assisted diagnosis and therapy of gastrointestinal submucosal tumors. Endosc Ultrasound 2013;2:125-33.

7. Alkhatib AA, Faigel DO. Endoscopic ultrasonographyguided diagnosis of subepithelial tumors. Gastrointest Endosc Clin N Am 2012;22:187-205.

8. Kongkam P, Devereaux BM, Ponnudurai R, et al. Endoscopic ultrasound forum summary from the Asian Pacifc digestive week endoscopic ultrasound 2012. Endosc Ultrasound 2013;2:43-60.

9. Nagler AK, Aslanian HR, Siddiqui UD. Endoscopic ultrasound and gastric lesions. J Clin Gastroenterol 2011;45:215-21.

10. Zhao H. China's surgical expert consensus on the diagnosis and treatment of cholangiocarcinoma: an interpretation. Hepatobiliary Surg Nutr 2013;2:288-9.

11. Vinayek R, Capurso G, Larghi A. Grading of EUSFNA cytologic specimens from patients with pancreatic neuroendocrine neoplasms: it is time move to tissue core biopsy? Gland Surg 2014;3:222-5.

12. Mahjoub AR, O’Reilly EM. Emerging therapies for pancreas neuroendocrine cancers. Chin Clin Oncol 2013;2:23.

13. Lin JL. T1 esophageal cancer, request an endoscopic mucosal resection (EMR) for in-depth review. J Thorac Dis 2013;5:353-6.

14. Ramesh J, Varadarajulu S. How can we get the best results with endoscopic ultrasound-guided fne needle aspiration? Clin Endosc 2012;45:132-7.

15. Cooper A, Aloia T. Surgical resection for hepatocellular carcinoma. Transl Cancer Res 2013;2:450-9.

16. Costache MI, Iordache S, Karstensen JG, et al. Endoscopic ultrasound-guided fne needle aspiration: from the past to the future. Endosc Ultrasound 2013;2:77-85.

17. Dumonceau JM, Polkowski M, Larghi A, et al. Indications, results, and clinical impact of endoscopic ultrasound (EUS)-guided sampling in gastroenterology: European society of gastrointestinal endoscopy (ESGE) clinical guideline. Endoscopy 2011;43:897-912.

18. Turner BG, Cizginer S, Agarwal D, et al. Diagnosis of pancreatic neoplasia with EUS and FNA: a report of accuracy. Gastrointest Endosc 2010;71:91-8.

19. Nguyen TQ, Kalade A, Prasad S, et al. Endoscopic ultrasound guided fne needle aspiration (EUS-FNA) of mediastinal lesions. ANZ J Surg 2011;81:75-8.

20. Konda VJ, Aslanian HR, Wallace MB, et al. First assessment of needle-based confocal laser endomicroscopy during EUS-FNA procedures of the pancreas (with videos). Gastrointest Endosc 2011;74:1049-60.

21. Saftoiu A, Vilmann P, Bhutani MS. Endoscopic Ultrasound-Guided Confocal Laser Endomicroscopy: Using the Optical Needle into the Acoustic Haystack. Euro J Ultrasound 2012;33:607-10.

22. Nakai Y, Iwashita T, Park DH, et al. Diagnosis of Pancreatic Cysts: Endoscopic Ultrasound, Through-the-Needle Confocal Laser-Induced Endomicroscopy and Cystoscopy Trial (Detect Study). Gastrointest Endosc 2012;75:AB145-6.

23. Giovannini M. Endoscopic ultrasound-guided confocal microscopy: a new tool for the new year? Endosc Ultrasound 2013;2:1-2.

24. Gheonea DI, Ciurea ME, S?ftoiu A, et al. Quantitative RTPCR analysis of MMR genes on EUS-guided FNA samples from focal pancreatic lesions. Hepatogastroenterology 2012;59:916-20.

25. Carrara S, Cangi MG, Arcidiacono PG, et al. Mucin expression pattern in pancreatic diseases: fndings from EUS-guided fne-needle aspiration biopsies. Am J Gastroenterol 2011;106:1359-63.

26. Khalid A, Nodit L, Zahid M, et al. Endoscopic ultrasound fne needle aspirate DNA analysis to differentiate malignant and benign pancreatic masses. Am J Gastroenterol 2006;101:2493-500.

27. Bournet B, Pointreau A, Souque A, et al. Gene expression signature of advanced pancreatic ductal adenocarcinoma using low density array on endoscopic ultrasound-guided fne needle aspiration samples. Pancreatology 2012;12:27-34.

28. Wang X, Gao J, Ren Y, et al. Detection of KRAS gene mutations in endoscopic ultrasound-guided fne-needle aspiration biopsy for improving pancreatic cancer diagnosis. Am J Gastroenterol 2011;106:2104-11.

29. Ogura T, Yamao K, Sawaki A, et al. Clinical impact of K-ras mutation analysis in EUS-guided FNA specimens from pancreatic masses. Gastrointest Endosc 2012;75:769-74.

30. Wang Y, Gao J, Li Z, et al. Diagnostic value of mucins (MUC1, MUC2 and MUC5AC) expression profle in endoscopic ultrasound-guided fne-needle aspiration specimens of the pancreas. Int J Cancer 2007;121:2716-22.

31. DeWitt J, LeBlanc J, McHenry L, et al. Endoscopicultrasound-guided fne-needle aspiration of ascites. Clin Gastroenterol Hepatol 2007;5:609-15.

32. Liu W, Sun S, Ge N, et al. Rupture of a duodenal stromal tumor during EUS-FNA: A case report. Endosc Ultrasound 2012;1:53-5.

33. S?ftoiu A, Vilmann P, Gorunescu F, et al. Neural network analysis of dynamic sequences of EUS elastography used for the differential diagnosis of chronic pancreatitis and pancreatic cancer. Gastrointest Endosc 2008;68:1086-94.

34. Iglesias-Garcia J, Larino-Noia J, Abdulkader I, et al. EUS elastography for the characterization of solid pancreatic masses. Gastrointest Endosc 2009;70:1101-8.

35. Giovannini M, Hookey LC, Bories E, et al. Endoscopic ultrasound elastography: the frst step towards virtual biopsy? Preliminary results in 49 patients. Endoscopy 2006;38:344-8.

36. Giovannini M, Thomas B, Erwan B, et al. Endoscopic ultrasound elastography for evaluation of lymph nodes and pancreatic masses: a multicenter study. World J Gastroenterol 2009;15:1587-93.

37. S?ftoiu A, Iordache SA, Gheonea DI, et al. Combined contrast-enhanced power Doppler and real-time sonoelastography performed during EUS, used in the differential diagnosis of focal pancreatic masses (with videos). Gastrointest Endosc 2010;72:739-47.

38. Sun SY, Liu X, Ge N, et al. EUS elastrography in lymph node staging of gastrointestinal tumor. Chin J Dig Endosc 2008;25:131-3.

39. Dawwas MF, Taha H, Leeds JS, et al. Diagnostic accuracy of quantitative EUS elastography for discriminating malignant from benign solid pancreatic masses: a prospective, single-center study. Gastrointest Endosc 2012;76:953-61.

40. Rustemovic N, Hrstic I, Opacic M, et al. EUS elastography in the diagnosis of focal liver lesions. Gastrointest Endosc 2007;66:823-4; discussion 824.

41. Iglesias García J, Lari?o Noia J, Souto R, et al. Endoscopic ultrasound (EUS) elastography of the liver. Rev Esp Enferm Dig 2009;101:717-9.

42. Iglesias-Garcia J, Lindkvist B, Lari?o-Noia J, et al. Endoscopic ultrasound elastography. Endosc Ultrasound 2012;1:8-16.

43. Dietrich CF, Ignee A, Frey H. Contrast-enhanced endoscopic ultrasound with low mechanical index: a new technique. Z Gastroenterol 2005;43:1219-23.

44. Dietrich CF, Sharma M, Hocke M. Contrast-enhanced endoscopic ultrasound. Endosc Ultrasound 2012;1:130-6.

45. Dietrich CF, Ignee A, Braden B, et al. Improved differentiation of pancreatic tumors using contrastenhanced endoscopic ultrasound. Clin Gastroenterol Hepatol 2008;6:590-597.e1.

46. Dietrich CF, Jenssen C, Hocke M, et al. Imaging of gastrointestinal stromal tumours with modern ultrasound techniques - a pictorial essay. Z Gastroenterol 2012;50:457-67.

47. Dietrich CF, Ignee A, Barreiros AP, et al. Contrastenhanced ultrasound for imaging of adrenal masses. Ultraschall Med 2010;31:163-8.

48. Friedrich-Rust M, Glasemann T, Polta A, et al. Differentiation between benign and malignant adrenal mass using contrast-enhanced ultrasound. Ultraschall Med 2011;32:460-71.

49. Hocke M, Menges M, Topalidis T, et al. Contrastenhanced endoscopic ultrasound in discrimination between benign and malignant mediastinal and abdominal lymph nodes. J Cancer Res Clin Oncol 2008;134:473-80.

50. Kitano M, Kudo M, Yamao K, et al. Characterization of small solid tumors in the pancreas: the value of contrastenhanced harmonic endoscopic ultrasonography. Am J Gastroenterol 2012;107:303-10.

51. Levy MJ, Topazian MD, Wiersema MJ, et al. Initial evaluation of the effcacy and safety of endoscopic ultrasound-guided direct Ganglia neurolysis and block. Am J Gastroenterol 2008;103:98-103.

52. Ascunce G, Ribeiro A, Reis I, et al. EUS visualization and direct celiac ganglia neurolysis predicts better pain relief in patients with pancreatic malignancy (with video). Gastrointest Endosc 2011;73:267-74.

53. Sakamoto H, Kitano M, Komaki T, et al. Endoscopic ultrasound-guided neurolysis in pancreatic cancer. Pancreatology 2011;11:52-8.

54. Guo X, Cui Z, Hu Z. Role of endoscopic ultrasound in treatment of pancreatic cancer. Endosc Ultrasound 2013;2:181-9.

55. Sun S, Qingjie L, Qiyong G, et al. EUS-guided interstitial brachytherapy of the pancreas: a feasibility study. Gastrointest Endosc 2005;62:775-9.

56. Sun S, Xu H, Xin J, et al. Endoscopic ultrasound-guided interstitial brachytherapy of unresectable pancreatic cancer: results of a pilot trial. Endoscopy 2006;38:399-403.

57. Jin Z, Du Y, Li Z, et al. Endoscopic ultrasonographyguided interstitial implantation of iodine 125-seeds combined with chemotherapy in the treatment of unresectable pancreatic carcinoma: a prospective pilot study. Endoscopy 2008;40:314-20.

58. Park WG, Yan BM, Schellenberg D, et al. EUS-guidedgold fducial insertion for image-guided radiation therapy of pancreatic cancer: 50 successful cases without fuoroscopy. Gastrointest Endosc 2010;71:513-8.

59. DiMaio CJ, Nagula S, Goodman KA, et al. EUS-guided fducial placement for image-guided radiation therapy in GI malignancies by using a 22-gauge needle (with videos). Gastrointest Endosc 2010;71:1204-10.

60. Carrara S, Arcidiacono PG, Albarello L, et al. Endoscopic ultrasound-guided application of a new hybrid cryotherm probe in porcine pancreas: a preliminary study. Endoscopy 2008;40:321-6.

61. Kim HJ, Seo DW, Hassanuddin A, et al. EUS-guided radiofrequency ablation of the porcine pancreas. Gastrointest Endosc 2012;76:1039-43.

62. Gaidhane M, Smith I, Ellen K, et al. Endoscopic Ultrasound-Guided Radiofrequency Ablation (EUS-RFA) of the Pancreas in a Porcine Model. Gastroenterol Res Pract 2012;2012:431451.

63. Di Matteo F, Martino M, Rea R, et al. EUS-guided Nd:YAG laser ablation of normal pancreatic tissue: a pilot study in a pig model. Gastrointest Endosc 2010;72:358-63.

64. Park do H, Song TJ, Eum J, et al. EUS-guided hepaticogastrostomy with a fully covered metal stent as the biliary diversion technique for an occluded biliary metal stent after a failed ERCP (with videos). Gastrointest Endosc 2010;71:413-9.

65. Artifon EL. Endoscopic ultrasound-guided biliary drainage. Endosc Ultrasound 2013;2:61-3.

66. Giovannini M, Moutardier V, Pesenti C, et al. Endoscopic ultrasound-guided bilioduodenal anastomosis: a new technique for biliary drainage. Endoscopy 2001;33:898-900.

67. Giovannini M, Dotti M, Bories E, et al. Hepaticogastrostomy by echo-endoscopy as a palliative treatment in a patient with metastatic biliary obstruction. Endoscopy 2003;35:1076-8.

68. Yamao K, Bhatia V, Mizuno N, et al. EUS-guided choledochoduodenostomy for palliative biliary drainage in patients with malignant biliary obstruction: results of longterm follow-up. Endoscopy 2008;40:340-2.

69. Artifon EL, Aparico D, Paione JB, et al. Biliary drainage in patients with unresectable, malignant obstruction where ERCP fails: endoscopic ultrasonography-guided choledochoduodenostomy versus percutaneous drainage. J Clin Gastroenterol 2012;46:768-74.

Cite this article as:Chen F. Endoscopic ultrasonography: an advancing option with duality in both diagnosis and treatment of gastrointestinal oncology. Chin J Cancer Res 2014;26(6):724-729. doi: 10.3978/j.issn.1000-9604.2014.12.14

10.3978/j.issn.1000-9604.2014.12.14

Submitted Oct 15, 2014. Accepted for publication Dec 02, 2014.