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Risk factors of extra-hepatic progression after transarterial chemoembolization for hepatocellular carcinoma patients: A retrospective study in 654 cases

Publication ,  Journal Article
Li, S; Wang, Q; Mei, J; Wang, J; Zhong, XP; Ling, Y; Guo, Z; Lu, LH; Wei, W; Guo, R
Published in: Journal of Cancer
January 1, 2019

Aim: To investigate the risk factors of extra-hepatic progression after TACE in HCC. Methods: The study population included 654 HCC patients who underwent TACE between October 2005 and September 2012. We collected and analyzed their clinical characteristics and survival information. TACE was performed as previously described with minor modifications. When necessary, superselective chemoembolization was performed through the segmental or subsegmental arteries, based on the tumor location and extent and hepatic function reserve. If stasis could not be achieved in a tumor-feeding artery, iodized oil was used solely in some patients. Embolization was then performed with injection of absorbable gelfoam particles (1-2 mm in diameter) through the angiographic catheter. Results: The tumor response to initial TACE was evaluated in 645 patients. The CR rate, response rate (RR), and disease control rate (DCR) were 9.92%, 25.89%, and 70.39%, respectively. The median overall survival (OS) period was 14.5 months. The 6-month, 1-, 2-, 3-, and 5-year OS rates were 75.5%, 55.0%, 33.9%, 22.8%, and 14.9%, respectively. The median progression-free survival (PFS) period was 4.3 months. The 6-month, 1-, 2-, 3-, and 5-year PFS rates were 40.7%, 27.1%, 16.7%, 13.9%, and 9.3%, respectively. One hundred and fifty patients developed extrahepatic progression during follow-up. We demonstrated that in the absence of radical treatment after initial TACE (p<0.001), the presence of extrahepatic metastasis before initial TACE (p<0.001), AST >45 U/L (p=0.024), ALB <35 g/L (p=0.012), and tumor response were evaluated as PD and SD after initial TACE (p<0.001) and were found to be independent predictors of a poorer prognosis of extrahepatic PFS. Conclusions: We identified risk factors for extrahepatic progression after TACE in HCC patients. Early combination treatment was strongly recommended in patients that met these risk factors.

Duke Scholars

Published In

Journal of Cancer

DOI

EISSN

1837-9664

Publication Date

January 1, 2019

Volume

10

Issue

20

Start / End Page

5007 / 5014

Related Subject Headings

  • 3211 Oncology and carcinogenesis
  • 1112 Oncology and Carcinogenesis
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Li, S., Wang, Q., Mei, J., Wang, J., Zhong, X. P., Ling, Y., … Guo, R. (2019). Risk factors of extra-hepatic progression after transarterial chemoembolization for hepatocellular carcinoma patients: A retrospective study in 654 cases. Journal of Cancer, 10(20), 5007–5014. https://doi.org/10.7150/jca.35355
Li, S., Q. Wang, J. Mei, J. Wang, X. P. Zhong, Y. Ling, Z. Guo, L. H. Lu, W. Wei, and R. Guo. “Risk factors of extra-hepatic progression after transarterial chemoembolization for hepatocellular carcinoma patients: A retrospective study in 654 cases.” Journal of Cancer 10, no. 20 (January 1, 2019): 5007–14. https://doi.org/10.7150/jca.35355.
Li S, Wang Q, Mei J, Wang J, Zhong XP, Ling Y, et al. Risk factors of extra-hepatic progression after transarterial chemoembolization for hepatocellular carcinoma patients: A retrospective study in 654 cases. Journal of Cancer. 2019 Jan 1;10(20):5007–14.
Li, S., et al. “Risk factors of extra-hepatic progression after transarterial chemoembolization for hepatocellular carcinoma patients: A retrospective study in 654 cases.” Journal of Cancer, vol. 10, no. 20, Jan. 2019, pp. 5007–14. Scopus, doi:10.7150/jca.35355.
Li S, Wang Q, Mei J, Wang J, Zhong XP, Ling Y, Guo Z, Lu LH, Wei W, Guo R. Risk factors of extra-hepatic progression after transarterial chemoembolization for hepatocellular carcinoma patients: A retrospective study in 654 cases. Journal of Cancer. 2019 Jan 1;10(20):5007–5014.

Published In

Journal of Cancer

DOI

EISSN

1837-9664

Publication Date

January 1, 2019

Volume

10

Issue

20

Start / End Page

5007 / 5014

Related Subject Headings

  • 3211 Oncology and carcinogenesis
  • 1112 Oncology and Carcinogenesis