TY - JOUR
T1 - Infiltrative Hepatocellular Carcinoma
T2 - Natural History and Comparison with Multifocal, Nodular Hepatocellular Carcinoma
AU - Yopp, Adam C.
AU - Mokdad, Ali
AU - Zhu, Hao
AU - Mansour, John C.
AU - Balch, Glen C.
AU - Choti, Michael A.
AU - Singal, Amit G.
N1 - Publisher Copyright:
© 2015, Society of Surgical Oncology.
PY - 2015/12/1
Y1 - 2015/12/1
N2 - Objective: The purpose of this study was to delineate infiltrating hepatocellular carcinoma (HCC) and to compare patient characteristics, tumor characteristics, and outcomes with patients presenting with HCC tumors of discrete, nodular morphology at a similar stage. Methods: Patient demographic and tumor characteristics of 224 patients diagnosed with infiltrative or advanced discrete, nodular HCC at the University of Texas Southwestern Medical Center were collected between January 2005 and December 2011. Patient demographics, tumor characteristics, treatment regimens, and overall survival were analyzed between the two groups. Results: Overall, 135 patients were diagnosed with infiltrative HCC compared with 89 patients with either T3a or T3b nodular, discrete HCC. Infiltrative HCC patients were more likely to have symptoms at presentation compared with the nodular HCC cohort, (95 vs. 78 %; p < 0.001). No difference in underlying liver function or etiology of liver disease between cohorts was observed. Patients with infiltrative HCC were more likely to have metastatic disease (53 vs. 35 %; p = 0.007) and malignant venous thrombus (75 vs. 62 %; p < 0.001) compared with the nodular group. Infiltrative HCC had a median survival of 1.9 months compared with 4.3 months in the nodular HCC group (p < 0.0001). Within the infiltrative HCC cohort, symptoms [hazard ratio (HR) 7.2, 95 % confidence interval (CI) 1.9–27], Child–Pugh class C (HR 3.9, 95 % CI 2.1–7.1), hepatic thrombus (HR 5.6, 95 % CI 1.9–16), and lack of treatment (HR 5.6, 95 % CI 2.1–14.6) were associated with worse survival. Conclusions: Infiltrative HCC had a worse outcome than nodular, discrete HCC most likely secondary to burden of tumor manifested by extrahepatic metastases, vascular invasion, higher α-fetoprotein levels, and a high degree of symptoms.
AB - Objective: The purpose of this study was to delineate infiltrating hepatocellular carcinoma (HCC) and to compare patient characteristics, tumor characteristics, and outcomes with patients presenting with HCC tumors of discrete, nodular morphology at a similar stage. Methods: Patient demographic and tumor characteristics of 224 patients diagnosed with infiltrative or advanced discrete, nodular HCC at the University of Texas Southwestern Medical Center were collected between January 2005 and December 2011. Patient demographics, tumor characteristics, treatment regimens, and overall survival were analyzed between the two groups. Results: Overall, 135 patients were diagnosed with infiltrative HCC compared with 89 patients with either T3a or T3b nodular, discrete HCC. Infiltrative HCC patients were more likely to have symptoms at presentation compared with the nodular HCC cohort, (95 vs. 78 %; p < 0.001). No difference in underlying liver function or etiology of liver disease between cohorts was observed. Patients with infiltrative HCC were more likely to have metastatic disease (53 vs. 35 %; p = 0.007) and malignant venous thrombus (75 vs. 62 %; p < 0.001) compared with the nodular group. Infiltrative HCC had a median survival of 1.9 months compared with 4.3 months in the nodular HCC group (p < 0.0001). Within the infiltrative HCC cohort, symptoms [hazard ratio (HR) 7.2, 95 % confidence interval (CI) 1.9–27], Child–Pugh class C (HR 3.9, 95 % CI 2.1–7.1), hepatic thrombus (HR 5.6, 95 % CI 1.9–16), and lack of treatment (HR 5.6, 95 % CI 2.1–14.6) were associated with worse survival. Conclusions: Infiltrative HCC had a worse outcome than nodular, discrete HCC most likely secondary to burden of tumor manifested by extrahepatic metastases, vascular invasion, higher α-fetoprotein levels, and a high degree of symptoms.
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U2 - 10.1245/s10434-015-4786-7
DO - 10.1245/s10434-015-4786-7
M3 - Article
C2 - 26245845
AN - SCOPUS:84952870633
SN - 1068-9265
VL - 22
SP - 1075
EP - 1082
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
ER -