Skip to main content

Advertisement

Log in

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

  • Original Article
  • Published:
International Journal of Clinical Oncology Aims and scope Submit manuscript

Abstract

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 μg/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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Llovet JM, Bruix J (2004) Unresectable hepatocellular carcinoma: meta-analysis of arterial embolization (letter). Radiology 230: 300–302

    Article  PubMed  Google Scholar 

  2. Neuhaus P, Klupp J, Langrehr J (2001) mTOR inhibitors: an overview. Liver Transpl 7:473–484

    Article  PubMed  CAS  Google Scholar 

  3. Ogawa T, Tokuda M, Tomizawa K, et al. (1998) Osteoblastic differentiation is enhanced by rapamycin in rat osteoblast-like osteo-sarcoma (ROS 17/2.8) cells. Biochem Biophys Res Commun 249:226–230

    Article  PubMed  CAS  Google Scholar 

  4. Hosoi H, Dilling MB, Shikata T, et al. (1999) Rapamycin causes poorly reversible inhibition of mTOR and induces p53-independent apoptosis in human rhabdomyosarcoma cells. Cancer Res 59:886–894

    PubMed  CAS  Google Scholar 

  5. Schumacher G, Oidtmann M, Rosewicz S, et al. (2002) Sirolimus inhibits growth of human hepatoma cells in contrast to tacrolimus, which promotes cell growth. Transplant Proc 34:1392–1393

    Article  PubMed  CAS  Google Scholar 

  6. Schumacher G, Oidtmann M, Rueggeberg A. (2005) Sirolimus inhibits growth of human hepatoma cells alone or combined with tacrolimus, while tacrolimus promotes cell growth. World J Gastroenterol 11:1420–1425

    PubMed  CAS  Google Scholar 

  7. Kim DH, Sarbassov DD, Ali SM, et al. (2002) mTOR interacts with raptor to form a nutrient-sensitive complex that signals to the cell growth machinery. Cell 110:163–175

    Article  PubMed  CAS  Google Scholar 

  8. Guba M, von Breitenbuch P, Steinbauer M, et al. (2002) Rapamycin inhibits primary and metastatic tumour growth by antiangiogenesis: involvement of vascular endothelial growth factor. Nat Med 8:128–135

    Article  PubMed  CAS  Google Scholar 

  9. Rizell M, Lindner P (2005) Inhibition of mTOR suppresses experimental liver tumours. Anticancer Res 25:789–793

    PubMed  CAS  Google Scholar 

  10. Roskamps T (2006) Liver stem cells and their implication in hepatocellular and cholangiocarcinoma. Oncogene 25:3818–3822

    Article  Google Scholar 

  11. Guba M, Koehl GE, Neppl E, et al. (2005) Dosing of rapamycin is critical to achieve an optimal antiangiogenic effect against cancer. Transpl Int 18:89–94

    Article  PubMed  CAS  Google Scholar 

  12. Franz DN, Leonard J, Tudor C, et al. (2006) Rapamycin causes regression of astrocytomas in tuberous sclerosis complex. Ann Neurol 59:490–498

    Article  PubMed  CAS  Google Scholar 

  13. Therasse P, Arbuck SG, Eisenhauer EA, et al. (2000) New guidelines to evaluate the response to treatment in solid tumors. J Natl Cancer Inst 92:205–216

    Article  PubMed  CAS  Google Scholar 

  14. Therasse P, Eisenhauer EA, Verweij J. (2006) RECIST revisited: a review of validation studies on tumour assessment. Eur J Cancer 42:1031–1039

    Article  PubMed  CAS  Google Scholar 

  15. Ratain MJ, Eckhardt G. (2004) Phase II studies of modern drugs directed against new targets: If you are fazed, too, then resist RECIST. J Clin Oncol 22:4442–4445

    Article  PubMed  Google Scholar 

  16. National Cancer Institute. Common terminology criteria for adverse events (CTCAE). Version 3.0 Published date June 10, 2003, Ncl, Rockville

  17. Rizell M, Cahlin C, Friman S, et al.(2005) Impressive regression of primary liver cancer after treatment with sirolimus. Acta Oncol 44:496

    Article  PubMed  Google Scholar 

  18. Xu X, Kobayashi S, Qiao W, et al.(2006) Induction of intrahepatic cholangiocellular carcinom by liver-specific disruption of Smad4 and Pten in mice. J Clin Invest 116:1843–1852

    Article  PubMed  CAS  Google Scholar 

  19. Sahin F, Kannangai R, Adegbola O, et al. (2004) mTor and p70 s6 kinase expression in primary liver neoplasms. Clin Cancer Res 10:8421–8425

    Article  PubMed  CAS  Google Scholar 

  20. Torimura T, Sata M, Ueno T, et al. (1998) Increased expression of vascular endothelial growth factor is associated with tumour progression in hepatocellular carcinoma. Hum Pathol 29:986–991

    Article  PubMed  CAS  Google Scholar 

  21. Wang T E, Kao C R, Chen L T, et al. (2004) Salvage therapy for hepatocellular carcinoma with thalidomide. World J Gastroenterol 10:649–653

    PubMed  CAS  Google Scholar 

  22. Schwartz J D, Schwartz M, Goldman D, et al. (2005) Bevacizumab in hepatocellular carcinoma (HCC) in patients without metastasis and without invasion of the portal vein. J Clin Oncol 2005 ASCO Annual Meeting Proceedings 23:412

    Google Scholar 

  23. Kneteman NM, Oberholzer J, Al Saghier M, et al. (2004) Sirolimusbased immunosuppression for liver transplantation in the presence of extended criteria for hepatocellular carcinoma. Liver Transpl 10:1301–1311

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Magnus Rizell.

Additional information

All authors contributed to the conception of the study, analysis of data, and writing of the communication

About this article

Cite this article

Rizell, M., Andersson, M., Cahlin, C. et al. Effects of the mTOR inhibitor sirolimus in patients with hepatocellular and cholangiocellular cancer. Int J Clin Oncol 13, 66–70 (2008). https://doi.org/10.1007/s10147-007-0733-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10147-007-0733-3

Key words

Navigation