» Articles » PMID: 11905412

Factors Predicting Response and Survival in 149 Patients with Unresectable Hepatocellular Carcinoma Treated by Combination Cisplatin, Interferon-alpha, Doxorubicin and 5-fluorouracil Chemotherapy

Overview
Journal Cancer
Publisher Wiley
Specialty Oncology
Date 2002 Mar 22
PMID 11905412
Citations 36
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The objective of the current study was to identify patient and disease related factors that influence response and survival for patients with unresectable hepatocellular carcinoma (HCC) who received a systemic combination chemotherapy consisting of cisplatin, alpha-interferon, doxorubicin, and 5-fluorouracil (PIAF).

Methods: From July 1996 to February 1999, 149 patients with unresectable HCC were treated with PIAF: cisplatin (20mg/m2 intravenously, Days 1-4), doxorubicin (40mg/m2 intravenously, Day 1), 5-fluorouracil (400mg/m2 intravenously, Days 1-4), and alpha-interferon (5MU/m2 subcutaneously, Days 1-4), once every 3 weeks up to a maximum of six cycles. Univariate and multivariate analyses of patient and disease characteristics were used to identify factors predicting response and survival.

Results: The objective response rate according to conventional criteria was 16.8% (complete response in 3 out of 149 patients, or 2%, 95% confidence interval [CI] 0-4.3%; partial response in 22 out of 149 patients, or 14.8%, 95% CI 9-20%). The median survival time was 30.9 weeks (95% CI 22.1 to 40). Significant independent predictors of an objective response were: absence of cirrhosis (P = 0.006), low bilirubin level (P = 0.006), and positive hepatitis C serology (P = 0.025). The following factors were related to a shorter survival time: high Okuda stage (P = 0.001), vascular involvement (P = 0.018), and cirrhosis (P = 0.008). Good risk patients (absence of cirrhosis and total bilirubin < or = 0.6mg/dL) had an objective response rate of 50%. CONCLUSIONS. Patients with unresectable HCC who also have normal total bilirubin and non-cirrhotic livers have a better chance of response and prolonged survival after treatment with systemic PIAF.

Citing Articles

Predicting the outcomes of hepatocellular carcinoma downstaging with the use of clinical and radiomics features.

Wang S, Sun K, Jin S, Wang K, Jiang N, Shan S BMC Cancer. 2023; 23(1):858.

PMID: 37700255 PMC: 10496191. DOI: 10.1186/s12885-023-11386-0.


Targeting Hypoxia-Inducible Factor-1α for the Management of Hepatocellular Carcinoma.

Huynh K, Rao S, Roth B, Bryan T, Fernando D, Dayyani F Cancers (Basel). 2023; 15(10).

PMID: 37345074 PMC: 10216171. DOI: 10.3390/cancers15102738.


Successful conversion therapy for unresectable hepatocellular carcinoma is getting closer: A systematic review and meta-analysis.

Pei Y, Li W, Wang Z, Liu J Front Oncol. 2022; 12:978823.

PMID: 36176393 PMC: 9513549. DOI: 10.3389/fonc.2022.978823.


Identification of a 3,3-difluorinated tetrahydropyridinol compound as a novel antitumor agent for hepatocellular carcinoma acting via cell cycle arrest through disturbing CDK7-mediated phosphorylation of Cdc2.

Bi W, Xiao J, Liu R, Zhou L, Zhang S, Yang M Invest New Drugs. 2019; 38(2):287-298.

PMID: 31076964 DOI: 10.1007/s10637-019-00792-6.


Cytotoxicity and Toxicity Evaluation of Xanthone Crude Extract on Hypoxic Human Hepatocellular Carcinoma and Zebrafish () Embryos.

Fazry S, Noordin M, Sanusi S, Noor M, Aizat W, Lazim A Toxics. 2018; 6(4).

PMID: 30304811 PMC: 6316214. DOI: 10.3390/toxics6040060.