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Cited 15 time in webofscience Cited 14 time in scopus
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Tumor Volume Doubling Time as a Dynamic Prognostic Marker for Patients with Hepatocellular Carcinoma

Authors
Kim, Jong KwanKim, Hyung-DonJun, Mi-JungYun, Sung-CheolShim, Ju HyunLee, Han ChuLee, DanbiAn, Ji hyunLim, Young-SukChung, Young-HwaLee, Yung SangKim, Kang Mo
Issue Date
Oct-2017
Publisher
SPRINGER
Keywords
Hepatocellular carcinoma; Tumor doubling time; Survival; Recurrence
Citation
DIGESTIVE DISEASES AND SCIENCES, v.62, no.10, pp.2923 - 2931
Indexed
SCIE
SCOPUS
Journal Title
DIGESTIVE DISEASES AND SCIENCES
Volume
62
Number
10
Start Page
2923
End Page
2931
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/3472
DOI
10.1007/s10620-017-4708-6
ISSN
0163-2116
Abstract
Background and Aims :To evaluate the clinical value of tumor growth rate in hepatocellular carcinoma (HCC) patients, we investigated the growth rate of HCC by calculating the tumor volume doubling time (TVDT) and its impact on survival and recurrence. Methods: A retrospective cohort study of 269 HCC patients who underwent two or more pretreatment imaging studies of computed tomography or magnetic resonance imaging was performed. Tumor growth rate and TVDT were calculated by comparing tumor volumes between imaging studies. Clinical parameters independently related to a TVDT of <2 months were evaluated. After dividing patients into slow-growing (159 patients with TVDT >2 months) and rapid-growing (110 patients with TVDT <2 months) groups, we compared the groups in terms of their survival and recurrence outcomes. The response to transarterial chemoembolization (TACE) was evaluated according to TVDT. Results: The median tumor growth rate and TVDT were 37.5%/month and 2.37 months, respectively. By logistic regression analyses, a high Child–Pugh score, small initial tumor diameter, gross vascular invasion, and tumor multiplicity were found to be independently associated with a TVDT of <2 months (P < 0.05). Patients in the rapid-growing group had lower survival rates and higher recurrence rates (P < 0.05). The response to TACE was worse in the rapid-growing group (P < 0.05). Conclusions: A fast HCC growth rate is associated with poor liver function and aggressive tumor biology. HCC patients with shorter TVDTs exhibit poorer survival and recurrence outcomes as well as a poor response to TACE.
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