Guidelines
Lipiodol® Ultra-Fluid
(Iodinated ethyl esters of fatty acids of poppy seed oil)
The AASLD recommends locoregional therapy over no treatment in adults with cirrhosis and HCC (T2 or T3, no vascular involvement) who are not candidates for resection or transplantation. (Quality/Certainty of Evidence for TACE = moderate).
A meta-analysis comparing TACE with placebo:
The analysis demonstrated improvement in 2-year survival for patients treated with TACE vs placebo (41% vs 27%; OR, 0.53; P = 0.017).
A meta-analysis specifically comparing DEB-TACE with conventional TACE treatment performed (3) identified 4 RCTs and 8 observational trials. Non-significant trends were noted in 1-, 2-, and 3-year survival in favor of DEB-TACE compared with conventional TACE. Pooled analysis of objective response and of complications showed no difference between the two therapies.
TACE is distinguished from TAE (transarterial embolization) in that,
The results of 2 RCTs and one retrospective case-control study have shown a survival benefit for TACE compared with supportive care in patients with unresectable HCC.
Arterially directed therapy (including TACE) is recommended in patients:
The BCLC recommends TACE for intermediate stage (B: multinodular, preserved liver function, performance status = 0), with well-defined nodules, preserved portal flow and selective access: expected survival > 2.5 years.
TACE might be performed using chemotherapy emulsified in lipiodol followed by gelfoam or any other material injection (conventional TACE) or using drug-eluting microspheres (DEB-TACE).
Response rates and survival are not different between the technique.
TACE is also recommended in not feasible or failure of ablation / resection / ablation / transplant of
- very early stages (0) : Single < 2 cm, preserved liver function, performance status = 0),
- early stage (A: single or < 3 nodules each < 3 cm, preserved liver function, performance status = 0): expected survival > 5 years.
For early stage (A: single or < 3 nodules each < 3cm preserved liver function, performance status = 0), upon enlisting patients for liver transplantation (LT) and if the expected waiting time exceeds 6 months, it is recommended to consider treatment to prevent tumour progression that could rule out LT. Ablation, chemoembolization and transarterial radioembolization are the most widely used options for this purpose.
TACE is recommended for patients with BCLC stage B and should be carried out in a selective manner (evidence high; recommendation strong).
The use of drug-eluting beads has shown similar benefit to conventional TACE (cTACE; gelfoam-Lipiodol® particles) and either of the two can be utilised (evidence high; recommendation strong).
TACE should not be used in patients with decompensated liver disease, advanced liver and/or kidney dysfunction, macroscopic vascular invasion or extrahepatic spread (evidence high; recommendation
strong).
There is insufficient evidence to recommend bland embolization, selective intra-arterial chemotherapy and lipiodolization (evidence moderate).
Recently, a systematic review on conventional TACE has included 101 articles , with a total of 10,108 patients.
The objective response rate was 52.5% (95% CI 43.6–61.5), and the overall survival (OS) was 70.3% at one year, 51.8% at two years, 40.4% at three years, and 32.4% at five years with a median OS of 19.4 months (95% CI 16.2–22.6).
The five most common adverse events were:
A retrospective study has shown that biliary injuries, intrahepatic bilioma, and global hepatic damage were significantly higher following DEB-TACE than with conventional TACE, especially in patients with advanced cirrhosis.
Modified BCLC staging system and treatment strategy
The benefit of TACE in prolonging OS was demonstrated in selected asymptomatic patients with maintained liver function that belong to the BCLC A stage to early intermediate BCLC B stage, who had a small tumor burden but were not amenable to surgery or local ablation [I, A: strong evidence for efficacy].
Median OS (mOS) of 30– 45 months can be expected in this population. Shorter median survival of < 20 months has been reported in real life cohorts when patients with no proven benefit are treated including those in Child-Pugh B stage, with portal vein invasion, large tumor burden or deteriorating liver function under TACE.
The text has been updated to include a level of evidence and grade of recommendation for selective internal radiotherapy (SIRT)
BCLC staging and treatment options according to level of evidence and approval status
TACE is currently recognized as one of the most commonly used nonsurgical treatments
for HCC (level 1 evidence).
Lipiodol emulsion (containing chemotherapy drugs), standardized gelatin sponge particles, blank microspheres, and polyvinyl alcohol particles are often used in conventional TACE (also known as cTACE).
Indications for TACE:
China clinical staging and treatment pathway for HCC
TACE :
For localized tumors, superselective infusion of Lipiodol® mixed with anticancer agents followed by gelatin sponge injection with visualization of portal branch improves the local treatment efficacy (20).
According to the 20th Nation-wide Follow-up Survey Report on Primary Liver Cancer, cTACE using Lipiodol® and gelatin sponge was performed as a first-line treatment in 27.5% (n = 5,083) of 18,458 initially diagnosed HCC cases and 39.3% (n = 2,627) of 6,687 recurrent cases of HCC, making it the most commonly used treatment for HCC.
Although TACE using drug-eluting beads (DEB) was introduced in Japan in 2014, cTACE remains the mainstream treatment for HCC, and the improved outcomes of cTACE have directly translated into prolonged survival of HCC patients.
The most recent meta-analysis, which was reported in 2016, included 1,449 patients from 4 randomized controlled trials and 8 observational studies. The results showed no significant difference between DEB-TACE and cTACE in terms of response rate, overall survival, or adverse events.
References
Clinical cases and Publications
Learn more about the clinical cases related to HCC management
Clinical Cases and PublicationsReferences
1.EASL-EORTC Clinical Practice Guidelines for the Management of Hepatocellular Carcinoma. J. Hepatol. 2018
2.ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up (eUpdate), 2020, https://www.esmo.org/guidelines/gastrointestinal-cancers/hepatocellular-carcinoma
3.US Guidelines: Bruix J. AASLD Practice Guidelines; American Association for Study of the Liver Diseases; Hepatology 2011; Vol. 53, No. 3.
4.Japanese Guidelines: Hepatology Research 2010; 40 (Suppl. 1): 96–112.
5.Chinese guidelines 2011 edition, Chin. Clin. Oncol. 2012; 1:10.
6.Takeuchi Y. et al., Guidelines for the use of NBCA in vascular embolization devised by the Committee of Practice Guidelines of the Japanese Society of Interventional Radiology (CGJSIR), 2012 edition, Jpn J Radiol, 2014; 32:500–517.
7.American Society for Gastrointestinal Endoscopy. Tissue adhesives: cyanoacrylate glue and fibrin sealant, Gastrointestinal Endoscopy, 2013;78: 2. 209-215.
8.LEE BB. et al., Consensus Document of the International Union of Angiology (IUA)-2013 Current concepts on the management of arterio-venous malformations, International Angiology, 2013;32(1):11-36.
9.Lee BB, et al., IUA-ISVI consensus for diagnosis guideline of chronic lymphedema of the limbs, Edizioni Minerva Medica, 2014,https://www.minervamedica.it/
10.Kimberly Levenhagen, et al., Diagnosis of Upper-Quadrant Lymphedema Secondary to Cancer: Clinical Practice Guideline From the Oncology Section of APTA, American Physical Therapy Association, Phys Ther, 2017;97: 729–745