Volume 17, Issue 8 pp. 889-896

Treatment of non-resectable hepatocellular carcinoma with autologous tumor-pulsed dendritic cells

Andrew Ladhams

Andrew Ladhams

Clinical Research Center, Royal Brisbane Hospital Research Foundation,

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Chris Schmidt

Chris Schmidt

Queensland Institute of Medical Research,

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Garwin Sing

Garwin Sing

Clinical Research Center, Royal Brisbane Hospital Research Foundation,

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Lesley Butterworth

Lesley Butterworth

Clinical Research Center, Royal Brisbane Hospital Research Foundation,

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George Fielding

George Fielding

Royal Brisbane Hospital,

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Paul Tesar

Paul Tesar

Royal Brisbane Hospital,

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Russell Strong

Russell Strong

Princess Alexandra Hospital, Brisbane, Queensland and

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Barbara Leggett

Barbara Leggett

Royal Brisbane Hospital,

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Lawrie Powell

Lawrie Powell

Queensland Institute of Medical Research,

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Guy Maddern

Guy Maddern

Queen Elizabeth II Hospital, Adelaide, South Australia, Australia

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Kay Ellem

Kay Ellem

Queensland Institute of Medical Research,

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Graham Cooksley

Corresponding Author

Graham Cooksley

Clinical Research Center, Royal Brisbane Hospital Research Foundation,

Professor G Cooksley, Clinical Research Center, Royal Brisbane Hospital Research Foundation, H Floor, Bancroft Center, Brisbane, Qld 4029, Australia. Email: [email protected]Search for more papers by this author
First published: 07 August 2002
Citations: 54

Abstract

Abstract Background: The response of hepatocellular carcinoma (HCC) to therapy is often disappointing and new modalities of treatment are clearly needed. Active immunotherapy based on the injection of autologous dendritic cells (DC) co-cultured ex vivo with tumor antigens has been used in pilot studies in various malignancies such as melanoma and lymphoma with encouraging results.

Methods: In the present paper, the preparation and exposure of patient DC to autologous HCC antigens and re-injection in an attempt to elicit antitumor immune responses are described.

Results: Therapy was given to two patients, one with hepatitis C and one with hepatitis B, who had large, multiple HCC and for whom no other therapy was available. No significant side-effects were observed. The clinical course was unchanged in one patient, who died a few months later. The other patient, whose initial prognosis was considered poor, is still alive and well more than 3 years later with evidence of slowing of tumor growth based on organ imaging.

Conclusions: It is concluded that HCC may be a malignancy worthy of DC trials and sufficient details in the present paper are given for the protocol to be copied or modified.

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