Literature DB >> 10430068

Complete pathological remission is possible with systemic combination chemotherapy for inoperable hepatocellular carcinoma.

T W Leung1, Y Z Patt, W Y Lau, S K Ho, S C Yu, A T Chan, T S Mok, W Yeo, C T Liew, N W Leung, A M Tang, P J Johnson.   

Abstract

The purpose of this Phase II study was to determine the response rate, the toxicity, and the effect on survival of the combination of cisplatin, doxorubicin, 5-fluorouracil, and alpha-IFN (PIAF) in advanced unresectable hepatocellular carcinoma. Fifty patients with either unresectable or metastatic disease were treated with PIAF: cisplatin (20 mg/m2 i.v., days 1-4), doxorubicin (40 mg/m2 i.v., day 1), 5-fluorouracil (400 mg/m2 i.v., days 1-4), and alpha-IFN (5 MU/m2 s.c., days 1-4). Treatment was repeated every 3 weeks to a maximum of six cycles. All patients were evaluable for response, toxicity, and survival. As assessed by conventional imaging criteria, there were no complete responses, but 13 patients (26%) had a partial response. Among the 36 patients who had an initially high alpha-fetoprotein level (>500 ng/ml), 15 (42%) had a >50% fall after therapy. Nine patients underwent surgical resection after achieving partial response and, in 4 of these patients, histological examination of the resected specimens revealed no viable tumor cells. All these nine patients are alive, and eight patients remain in complete remission at between 7.6 and 25.8 months at the time of analysis. The overall median survival was 8.9 months. Toxicity was mainly myelosuppression and mucositis. There were two treatment-related deaths due to neutropenic sepsis. PIAF is active in hepatocellular carcinoma despite considerable hematological toxicity. Complete pathological remission is possible with this systemic combination. Apparently, persistent radiological lesions may still represent complete pathological resolution of active disease.

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Year:  1999        PMID: 10430068

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  60 in total

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Review 2.  Hepatocellular carcinoma.

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Journal:  Curr Treat Options Oncol       Date:  2000-12

3.  miR-221 silencing blocks hepatocellular carcinoma and promotes survival.

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4.  Antiproliferation and apoptosis induction of paeonol in HepG2 cells.

Authors:  Shu-Ping Xu; Guo-Ping Sun; Yu-Xian Shen; Wei Wei; Wan-Ren Peng; Hua Wang
Journal:  World J Gastroenterol       Date:  2007-01-14       Impact factor: 5.742

5.  Non-surgical treatment of hepatocellular carcinoma.

Authors:  Philip J Johnson
Journal:  HPB (Oxford)       Date:  2005       Impact factor: 3.647

Review 6.  Hepatocellular carcinoma: is current therapy really altering outcome?

Authors:  P J Johnson
Journal:  Gut       Date:  2002-10       Impact factor: 23.059

7.  Highlights for α-fetoprotein in determining prognosis and treatment monitoring for hepatocellular carcinoma.

Authors:  Xin-Sen Xu; Kai Qu; Chang Liu; Yue-Lang Zhang; Jun Liu; Yan-Zhou Song; Peng Zhang; Si-Nan Liu; Hu-Lin Chang
Journal:  World J Gastroenterol       Date:  2012-12-28       Impact factor: 5.742

Review 8.  Management of hepatocellular cancer.

Authors:  Mary F Mulcahy
Journal:  Curr Treat Options Oncol       Date:  2005-09

Review 9.  Chemotherapy and target therapy for hepatocellular carcinoma: New advances and challenges.

Authors:  Gan-Lu Deng; Shan Zeng; Hong Shen
Journal:  World J Hepatol       Date:  2015-04-18

10.  CpG oligodeoxynucleotides inhibit tumor growth and reverse the immunosuppression caused by the therapy with 5-fluorouracil in murine hepatoma.

Authors:  Xian-Song Wang; Zhen Sheng; You-Bing Ruan; Yang Guang; Mu-Lan Yang
Journal:  World J Gastroenterol       Date:  2005-02-28       Impact factor: 5.742

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