Efficacy and safety of endoscopic ultrasonography-guided interventional treatment for refractory malignant left-sided liver tumors: a case series of 26 patients

Tian-An Jiang, Zhuang Deng, Guo Tian, Qi-Yu Zhao, Wei-Lin Wang, Tian-An Jiang, Zhuang Deng, Guo Tian, Qi-Yu Zhao, Wei-Lin Wang

Abstract

This study aimed to compare the efficacy and safety of EUS-guided ethanol injection and 125I seed brachytherapy for malignant left-sided liver tumors which were difficult for trans-abdominal intervention. The study protocol was registered at Clinicaltrials.gov (NCT02816944). Twenty-six patients were consecutively and prospectively hospitalized for EUS-guided interventional treatment of refractory malignant left-sided liver tumors between June 2014 and June 2016. Liver masses were detected using EUS in 25 of 26 (96.2%) patients. EUS-guided interventional treatment was completed uneventfully in 23 of 26 (88.5%) patients using anhydrous ethanol injection (n = 10) or iodine-125 seed implantation (n = 13). Six months later, complete response was achieved in 15 of 23 (65.2%) patients and partial response in 8 of 23 (34.8%) patients. Patients with tumor residual have second-look EUS-guided interventional treatment (n = 5), radiotherapy (n = 2) or surgical resection (n = 1). Complete response was achieved after repeated interventional treatment in 3 of 5 patients who underwent second EUS-guided intervention; 2 patients required additional surgical resection but one succeed. No significant complications occurred. Therefore EUS-guided 125I seed brachytherapy is an effective and safe treatment modality for radical operation or promising palliative control of malignant left-sided liver tumors refractory to trans-abdominal intervention.

Figures

Figure 1. EUS-guided iodine-125 brachytherapy for postoperative…
Figure 1. EUS-guided iodine-125 brachytherapy for postoperative liver metastasis of cholangiocarcinoma.
(A) presence of a 1.3-cm, low-density liver mass located in the left lobe on CT scan (white arrows). US image failed to show the lesions due to the gas ahead; (B) identification of a 1.5 cm × 1.3 cm low-echodensity mass on EUS (white arrows); (C) EUS-guided implantation of iodine-125 particles (white arrows); (D) obvious downsizing of the liver disease on follow-up CT scan at 1 months (white arrows); and (E) disappearance of the liver disease on follow-up MRI scan taken after 12 months.
Figure 2. EUS-guided anhydrous ethanol ablation for…
Figure 2. EUS-guided anhydrous ethanol ablation for postoperative liver recurrence of hepatocellular carcinoma.
(A) presence of a 1.5 cm × 1.1 cm postoperative liver recurrence located on the resection margin as shown on T2-weighted MRI scans (white arrows), but conventional US image failed to show the lesions; (B) EUS-guided ethanol injection; and (C) arterial phase (arrowhead) and (D) parenchymal phase (arrowhead): non-enhanced liver disease on follow-up contrast CT scan revealed complete resolution of disease at 12 months.
Figure 3. EUS-guided anhydrous ethanol ablation for…
Figure 3. EUS-guided anhydrous ethanol ablation for lesions in liver caudate lobe.
MRI imaging in liver caudate lobe showed a lesion of low T1 signal intensity (A) (arrowhead) and significant enhancement in arterial phase (B) (arrowhead). (C) at liver caudate lobe EUS scan showed a well-defined hypoechoic 1.9*1.6 cm lesion (arrows). (D) It indicated that 22G biopsy needle with EUS guidance was inserted into the lesion along with the needle sheath (arrowhead), and (E) diffuse increase in echogenicity covering the whole mass after the percutaneously punctured injection of anhydrous alcohol. After 1 month follow-up, MR scan was seen high T1-weighted signal intensity (F) (arrowhead) and no obvious enhancement during arterial (G) (arrowhead) and substance phase (H) (arrowhead). After 15 months follow-up, it showed high T1-weighted signal intensity (I) (arrowhead) and contrast material-enhanced MR images showed completed ablation without enhanced lesions (J) (arrowhead).

References

    1. Fowler K. J., Saad N. E. & Linehan D. Imaging approach to hepatocellular carcinoma, cholangiocarcinoma, and metastatic colorectal cancer. Surgical oncology clinics of North America 24, 19–40, doi: 10.1016/j.soc.2014.09.002 (2015).
    1. Pichlmayr R., Weimann A., Tusch G. & Schlitt H. J. Indications and Role of Liver Transplantation for Malignant Tumors. The oncologist 2, 164–170 (1997).
    1. Khan K., Wale A., Brown G. & Chau I. Colorectal cancer with liver metastases: neoadjuvant chemotherapy, surgical resection first or palliation alone? World journal of gastroenterology 20, 12391–12406, doi: 10.3748/wjg.v20.i35.12391 (2014).
    1. Wang H. M. et al.. Analysis of facial bone wall dimensions and sagittal root position in the maxillary esthetic zone: a retrospective study using cone beam computed tomography. The International journal of oral & maxillofacial implants 29, 1123–1129, doi: 10.11607/jomi.3348 (2014).
    1. Takayasu K. et al.. Prospective cohort study of transarterial chemoembolization for unresectable hepatocellular carcinoma in 8510 patients. Gastroenterology 131, 461–469, doi: 10.1053/j.gastro.2006.05.021 (2006).
    1. Horiguchi Y. et al.. Treatment of choice for unresectable small liver cancer: percutaneous ethanol injection therapy or transarterial chemoembolization therapy. Cancer chemotherapy and pharmacology 33 Suppl, S111–S114 (1994).
    1. Hoang N. H., Murad H. Y., Ratnayaka S. H., Chen C. & Khismatullin D. B. Synergistic ablation of liver tissue and liver cancer cells with high-intensity focused ultrasound and ethanol. Ultrasound in medicine & biology 40, 1869–1881, doi: 10.1016/j.ultrasmedbio.2014.02.026 (2014).
    1. Weis S., Franke A., Mossner J., Jakobsen J. C. & Schoppmeyer K. Radiofrequency (thermal) ablation versus no intervention or other interventions for hepatocellular carcinoma. The Cochrane database of systematic reviews, CD003046, doi: 10.1002/14651858.CD003046.pub3 (2013).
    1. Chen K. et al.. Adjuvant iodine-125 brachytherapy for hepatocellular carcinoma after complete hepatectomy: a randomized controlled trial. PloS one 8, e57397, doi: 10.1371/journal.pone.0057397 (2013).
    1. Wang J. D. et al.. Optimal treatment opportunity for mTHPC-mediated photodynamic therapy of liver cancer. Lasers in medical science 28, 1541–1548, doi: 10.1007/s10103-012-1248-3 (2013).
    1. Holt B. & Varadarajulu S. Endoscopic ultrasound-guided fine needle aspiration or fine needle biopsy: the beauty is in the eye of the beholder. Endoscopy 46, 1046–1048 (2014).
    1. Nakaji S., Hirata N., Kobayashi M., Shiratori T. & Sanagawa M. Endoscopic ultrasonography-guided ethanol injection as a treatment for ruptured hepatocellular carcinoma in the left hepatic lobe. Endoscopy 47 Suppl 1, E558–E560, doi: 10.1055/s-0034-1393394 (2015).
    1. Nakaji S. et al.. Endoscopic ultrasound (EUS)-guided ethanol injection for hepatocellular carcinoma difficult to treat with percutaneous local treatment. Endoscopy 44 Suppl 2 UCTN, E380, doi: 10.1055/s-0032-1309918 (2012).
    1. Azab M. et al.. Radiofrequency ablation combined with percutaneous ethanol injection in patients with hepatocellular carcinoma. Arab journal of gastroenterology: the official publication of the Pan-Arab Association of Gastroenterology 12, 113–118, doi: 10.1016/j.ajg.2011.07.005 (2011).
    1. Giorgio A. et al.. Percutaneous radiofrequency ablation of hepatocellular carcinoma compared to percutaneous ethanol injection in treatment of cirrhotic patients: an Italian randomized controlled trial. Anticancer research 31, 2291–2295 (2011).
    1. Brunello F. et al.. Radiofrequency ablation versus ethanol injection for early hepatocellular carcinoma: A randomized controlled trial. Scandinavian journal of gastroenterology 43, 727–735, doi: 10.1080/00365520701885481 (2008).
    1. Shiina S. et al.. A randomized controlled trial of radiofrequency ablation with ethanol injection for small hepatocellular carcinoma. Gastroenterology 129, 122–130 (2005).
    1. Zhang W. et al.. Placement of (1)(2)(5)I seed strands and stents for a type IV Klatskin tumor. World journal of gastroenterology 21, 373–376, doi: 10.3748/wjg.v21.i1.373 (2015).
    1. Luo J., Yan Z., Liu Q., Qu X. & Wang J. Endovascular placement of iodine-125 seed strand and stent combined with chemoembolization for treatment of hepatocellular carcinoma with tumor thrombus in main portal vein. Journal of vascular and interventional radiology: JVIR 22, 479–489, doi: 10.1016/j.jvir.2010.11.029 (2011).
    1. Zhang F. J. et al.. CT guided 125iodine seed implantation for portal vein tumor thrombus in primary hepatocellular carcinoma. Chinese medical journal 121, 2410–2414 (2008).
    1. Nag S., DeHaan M., Scruggs G., Mayr N. & Martin E. W. Long-term follow-up of patients of intrahepatic malignancies treated with iodine-125 brachytherapy. International journal of radiation oncology, biology, physics 64, 736–744, doi: 10.1016/j.ijrobp.2005.08.029 (2006).
    1. Bang J. Y. & Varadarajulu S. Endoscopic ultrasound-guided management of pancreatic pseudocysts and walled-off necrosis. Clinical endoscopy 47, 429–431, doi: 10.5946/ce.2014.47.5.429 (2014).
    1. Puspok A. et al.. Endoscopic ultrasound guided therapy of benign and malignant biliary obstruction: a case series. The American journal of gastroenterology 100, 1743–1747, doi: 10.1111/j.1572-0241.2005.41806.x (2005).
    1. Artifon E. L. et al.. Endoscopic ultrasound-guided choledochoduodenostomy and duodenal stenting in patients with unresectable periampullary cancer: one-step procedure by using linear echoendoscope. Scandinavian journal of gastroenterology 48, 374–379, doi: 10.3109/00365521.2012.763176 (2013).
    1. Zhang W. Y., Li Z. S. & Jin Z. D. Endoscopic ultrasound-guided ethanol ablation therapy for tumors. World journal of gastroenterology 19, 3397–3403, doi: 10.3748/wjg.v19.i22.3397 (2013).
    1. Awad S. S. et al.. Preoperative evaluation of hepatic lesions for the staging of hepatocellular and metastatic liver carcinoma using endoscopic ultrasonography. American journal of surgery 184, 601-604; discussion 604–605 (2002).
    1. Singh P. et al.. Endoscopic ultrasound versus CT scan for detection of the metastases to the liver: results of a prospective comparative study. Journal of clinical gastroenterology 43, 367–373, doi: 10.1097/MCG.0b013e318167b8cc (2009).
    1. Tonozuka R. et al.. EUS-guided drainage of hepatic abscess and infected biloma using short and long metal stents (with videos). Gastrointestinal endoscopy 81, 1463–1469, doi: 10.1016/j.gie.2015.01.023 (2015).
    1. Eso Y., Marusawa H., Tsumura T., Okabe Y. & Osaki Y. Endoscopic ultrasonography-guided transgastric drainage of infectious biloma following radiofrequency ablation for hepatocellular carcinoma. Digestive endoscopy: official journal of the Japan Gastroenterological Endoscopy Society 24, 390, doi: 10.1111/j.1443-1661.2012.01305.x (2012).
    1. Silva M. F. et al.. m-RECIST at 1 month and Child A are survival predictors after percutaneous ethanol injection of hepatocellular carcinoma. Annals of hepatology 13, 796–802 (2014).
    1. Zhuang H. Q., Wang J. J., Liao A. Y., Wang J. D. & Zhao Y. The biological effect of 125I seed continuous low dose rate irradiation in CL187 cells. Journal of experimental & clinical cancer research: CR 28, 12, doi: 10.1186/1756-9966-28-12 (2009).
    1. Xiang G. A., Chen K. Y., Wang H. N. & Xiao J. F. [Immunological influence of iodine-125 implantation in patients with hepatocellular carcinoma resection]. Nan fang yi ke da xue xue bao = Journal of Southern Medical University 30, 292–294 (2010).

Source: PubMed

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