Literature DB >> 23374360

Best radiological response to trans-arterial chemoembolization for hepatocellular carcinoma does not imply better outcomes.

Jon C Henry1, Lavina Malhotra, Hooman Khabiri, Gregory Guy, Anthony Michaels, James Hanje, Marcela Azevedo, Mark Bloomston, Carl R Schmidt.   

Abstract

INTRODUCTION: Regional therapy with trans-arterial chemoembolization (TACE) is a common treatment for unresectable hepatocellular carcinoma (HCC). Outcomes were examined in patients with the best radiological response (BR) after the initial TACE.
METHODS: This was a retrospective cohort study of patients who underwent TACE as the initial treatment for HCC between the years 2000 and 2010. BR was defined as complete disappearance of the tumour or no enhancement with contrast on the first cross-sectional imaging study after the initial TACE.
RESULTS: Seventy-eight out of 104 total consecutive patients were identified with the potential for a BR to TACE therapy for unresectable HCC, and 24 met the criteria for BR. Patients with BR had a median survival of 12.8 months (2.2-54.9) compared with 18.9 months(1.3-56.7) for the entire cohort (P= 0.313). The median time to progression was 10.6 months (1.2-24.3) in the BR group and 3.2 months (0.7-49.2) in the patients without a BR (P= 0.003). DISCUSSION: BR to initial TACE for unresectable HCC is associated with comparable survival to those without BR in spite of a longer time to cancer progression. It may be reasonable to consider further therapy such as repeat TACE or biological/systemic therapy in patients with HCC even when the radiological response to the initial TACE is favourable.
© 2012 International Hepato-Pancreato-Biliary Association.

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Year:  2012        PMID: 23374360      PMCID: PMC3572280          DOI: 10.1111/j.1477-2574.2012.00529.x

Source DB:  PubMed          Journal:  HPB (Oxford)        ISSN: 1365-182X            Impact factor:   3.647


  21 in total

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2.  Transcatheter arterial chemoembolisation for hepatocellular carcinoma in cirrhosis: survival rate and prognostic factors.

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3.  Previous chemoembolization response after transcatheter arterial chemoembolization (TACE) can predict the anti-tumor effect of subsequent TACE with miriplatin in patients with recurrent hepatocellular carcinoma.

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Authors:  Renumathy Dhanasekaran; David A Kooby; Charles A Staley; John S Kauh; Vinit Khanna; Hyun S Kim
Journal:  HPB (Oxford)       Date:  2010-04       Impact factor: 3.647

5.  Liver failure after transarterial chemoembolization for patients with hepatocellular carcinoma and ascites: incidence, risk factors, and prognostic prediction.

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Authors:  Ju Hyun Shim; Kang Mo Kim; Young-Joo Lee; Gi-Young Ko; Hyun-Ki Yoon; Kyu-Bo Sung; Kwang-Min Park; Sung-Gyu Lee; Young-Suk Lim; Han Chu Lee; Young-Hwa Chung; Yung Sang Lee; Dong Jin Suh
Journal:  Ann Surg Oncol       Date:  2009-12-22       Impact factor: 5.344

10.  Prognostic factors and treatment effects for hepatocellular carcinoma in Child C cirrhosis.

Authors:  K Nouso; Ym Ito; K Kuwaki; Y Kobayashi; S Nakamura; Y Ohashi; K Yamamoto
Journal:  Br J Cancer       Date:  2008-03-18       Impact factor: 7.640

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1.  Expression Patterns of Tumor Markers in Liver Transplant Recipients Showing Complete Pathological Response of Hepatocellular Carcinoma.

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2.  Extended postinterventional tumor necrosis-implication for outcome in liver transplant patients with advanced HCC.

Authors:  Arno Kornberg; Ulrike Witt; Edouard Matevossian; Bernadett Küpper; Volker Assfalg; Alexander Drzezga; Norbert Hüser; Moritz Wildgruber; Helmut Friess
Journal:  PLoS One       Date:  2013-01-22       Impact factor: 3.240

3.  Superparamagnetic iron oxide nanoparticles mediated (131)I-hVEGF siRNA inhibits hepatocellular carcinoma tumor growth in nude mice.

Authors:  Jing Chen; Shu Zhu; Liangqian Tong; Jiansha Li; Fei Chen; Yunfeng Han; Ming Zhao; Wei Xiong
Journal:  BMC Cancer       Date:  2014-02-21       Impact factor: 4.430

4.  Superparamagnetic iron oxide nanoparticles modified with polyethylenimine and galactose for siRNA targeted delivery in hepatocellular carcinoma therapy.

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  4 in total

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