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Effects of the mTOR inhibitor sirolimus in patients with hepatocellular and cholangiocellular cancer.

Rizell, Magnus, 1963 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Andersson, Mats, 1954 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Cahlin, Christian, 1959 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
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Hafström, Lars-Olof, 1936 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Olausson, Michael, 1956 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Lindnér, Per, 1956 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
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 (creator_code:org_t)
2008-02-29
2008
English.
In: International journal of clinical oncology / Japan Society of Clinical Oncology. - : Springer Science and Business Media LLC. - 1341-9625. ; 13:1, s. 66-70
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: Hepatocellular cancer (HCC), as well as cholangiocellular cancer (CCC), has an extremely poor prognosis due to the extent of tumor at diagnosis and the underlying liver disease. Sirolimus is used in the transplantation setting as an immunosuppressive agent, but it also possesses antiproliferative and antiangiogenic properties. The objective of the study was to evaluate the effect of sirolimus on HCC and CCC. METHODS: In a prospective single-arm protocol, the tumor response to sirolimus as the primary endpoint was studied in 21 patients with advanced HCC and nine with CCC. Sirolimus was administered once daily by mouth, with the dose adjusted to a serum trough level between 4 and 15 mug/ml. Tumor response was evaluated by computed tomography (CT) or magnetic resonance imaging (MRI), according to the Response Evaluation Criteria in Solid Tumors (RECIST), every third month. Secondary measures were overall survival, time to tumor progression, tumor markers, and side effects. RESULTS: Of the patients with HCC, one had partial remission (PR) and fi ve patients had stable disease (SD) at 3 months. Of the patients with CCC, three had SD. The median survival for patients with HCC was 6.5 months (range, 0.2-36 months) and that for patients with CCC was 7 months (range, 2.6-35 months). CONCLUSION: Treatment of HCC and CCC with sirolimus can induce temporary PD or SD. This pilot study indicates that sirolimus might be a promising drug for this treatment, but further clinical studies elucidating the biological effects are advocated.

Keyword

1-Phosphatidylinositol 3-Kinase
antagonists & inhibitors
Adult
Aged
Antibiotics
Antineoplastic
therapeutic use
Bile Duct Neoplasms
diagnosis
drug therapy
mortality
Bile Ducts
Intrahepatic
Carcinoma
Hepatocellular
diagnosis
drug therapy
mortality
Cholangiocarcinoma
diagnosis
drug therapy
mortality
Female
Humans
Liver Neoplasms
diagnosis
drug therapy
mortality
Male
Middle Aged
Protein Kinases
metabolism
Sirolimus
therapeutic use

Publication and Content Type

ref (subject category)
art (subject category)

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