Hormones and Cancer

, Volume 2, Issue 6, pp 385–392

Targeted Therapies for Adrenocortical Carcinoma: IGF and Beyond

  • Michael J. Demeure
  • Kimberly J. Bussey
  • Lawrence S. Kirschner
Article

DOI: 10.1007/s12672-011-0090-6

Cite this article as:
Demeure, M.J., Bussey, K.J. & Kirschner, L.S. HORM CANC (2011) 2: 385. doi:10.1007/s12672-011-0090-6

Abstract

Standard chemotherapy for adrenocortical cancer currently is under evaluation in the context of the recently completed FIRM-ACT evaluating the combination of mitotane with either streptozocin or etoposide, cisplatin, and doxorubicin. New agents are eagerly sought by the ACC community that hopes to make progress against this deadly disease. Investigators have begun to dissect the molecular and genomic context of ACC with a goal of identifying potential novel therapeutic agents. One gene consistently overexpressed in ACC is insulin growth factor type 2. Targeting its receptor IGF1R has shown encouraging results in ACC cell lines and against murine xenografts. As a result, clinical trials to evaluate agents targeting the IGF1R have been done including mitotane and IMC-A12 (a monoclonal antibody) and the GALACCTIC trial that has just completed accrual to evaluate OSI-906, a small molecule IGF1R antagonist. On the horizon are other agents targeting other tyrosine kinases, including EGF and FGF, and novel strategies such as individualized tumor analysis to select treatment.

Keywords

Adrenocortical cancerTargeted therapyIGF1RTyrosine Kinase inhibitors

Copyright information

© Springer Science+Business Media, LLC 2011

Authors and Affiliations

  • Michael J. Demeure
    • 1
  • Kimberly J. Bussey
    • 1
  • Lawrence S. Kirschner
    • 2
  1. 1.Clinical Translational Research DivisionTranslational Genomics Research InstitutePhoenixUSA
  2. 2.Department of Endocrinology, Diabetes, and MetabolismThe Ohio State UniversityColumbusUSA