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Does the Degree of Hepatocellular Carcinoma Tumor Necrosis following Transarterial Chemoembolization Impact Patient Survival?

Authors :
Haywood N
Gennaro K
Obert J
Sauer PF Jr
Redden DT
Zarzour J
Smith JK
Bolus D
Saddekni S
Aal AK
Gray S
White J
Eckhoff DE
DuBay DA
Source :
Journal of oncology [J Oncol] 2016; Vol. 2016, pp. 4692139. Date of Electronic Publication: 2016 Feb 02.
Publication Year :
2016

Abstract

Purpose. The association between transarterial chemoembolization- (TACE-) induced HCC tumor necrosis measured by the modified Response Evaluation Criteria In Solid Tumors (mRECIST) and patient survival is poorly defined. We hypothesize that survival will be superior in HCC patients with increased TACE-induced tumor necrosis. Materials and Methods. TACE interventions were retrospectively reviewed. Tumor response was quantified via dichotomized (responders and nonresponders) and the four defined mRECIST categories. Results. Median survival following TACE was significantly greater in responders compared to nonresponders (20.8 months versus 14.9 months, p = 0.011). Survival outcomes also significantly varied among the four mRECIST categories (p = 0.0003): complete, 21.4 months; partial, 20.8; stable, 16.8; and progressive, 7.73. Only progressive disease demonstrated significantly worse survival when compared to complete response. Multivariable analysis showed that progressive disease, increasing total tumor diameter, and non-Child-Pugh class A were independent predictors of post-TACE mortality. Conclusions. Both dichotomized (responders and nonresponders) and the four defined mRECIST responses to TACE in patients with HCC were predictive of survival. The main driver of the survival analysis was poor survival in the progressive disease group. Surprisingly, there was small nonsignificant survival benefit between complete, partial, and stable disease groups. These findings may inform HCC treatment decisions following first TACE.

Details

Language :
English
ISSN :
1687-8450
Volume :
2016
Database :
MEDLINE
Journal :
Journal of oncology
Publication Type :
Academic Journal
Accession number :
26949394
Full Text :
https://doi.org/10.1155/2016/4692139