Research Papers:

Detecting predictive androgen receptor modifications in circulating prostate cancer cells

Julie Steinestel _, Manuel Luedeke, Annette Arndt, Thomas J. Schnoeller, Jochen K. Lennerz, Carina Wurm, Christiane Maier, Marcus V. Cronauer, Konrad Steinestel, Andres J. Schrader

Metrics: PDF 1609 views  |   HTML 573 views  |   ?  


Julie Steinestel1,2,*, Manuel Luedeke1,*, Annette Arndt3,*, Thomas J. Schnoeller1, Jochen K. Lennerz4, Carina Wurm1, Christiane Maier1, Marcus V. Cronauer1, Konrad Steinestel5 and Andres J. Schrader1,2

1 Clinic of Urology, University Hospital Ulm, Ulm, Germany

2 Clinic of Urology, University Hospital Muenster, Muenster, Germany

3 Institute of Pathology and Molecular Pathology, Bundeswehrkrankenhaus Ulm, Ulm, Germany

4 Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA

5 Gerhard-Domagk Institute of Pathology, University of Muenster, Muenster, Germany

* These authors have contributed equally to the work

Correspondence to:

Julie Steinestel, email:

Keywords: castration-resistant prostate cancer, androgen receptor modification, splice variants, circulating tumor cells

Received: March 20, 2015 Accepted: April 07, 2015 Published: April 23, 2015


Molecular modifications of the androgen receptor (AR) can cause resistance to androgen deprivation therapy (ADT) in prostate cancer patients. Since lack of representative tumor samples hinders therapy adjustments according to emerging AR-modifications, we evaluated simultaneous detection of the two most common AR modifications (AR-V7 splice variant and AR point mutations) in circulating tumor cells (CTCs). We devised a single-tube assay to detect AR-V7 splice variants and AR point mutations in CTCs using immunomagnetic cell isolation, followed by quantitative real-time PCR and DNA pyrosequencing. We prospectively investigated 47 patients with PSA progression awaiting therapy switch. Comparison of response to newly administered therapy and CTC-AR-status allowed effect size estimation. Nineteen (51%) of 37 patients with detectable CTCs carried AR-modifications. Seventeen patients carried the AR-V7 splice variant, one harbored a p.T878A point mutation and one harbored both AR-V7 and a p.H875Y mutation. We estimated a positive predictive value for response and non-response to therapy by AR status in CTCs of ~94%. Based on a conservative calculation, we estimated the effect size for molecularly-informed therapy switches for prospective clinical trial planning to ~27%. In summary, the ability to determine key resistance-mediating AR modifications in CTCs has the potential to considerably improve prostate cancer treatment.

Author Information

Julie Steinestel
Primary Contact  _

Manuel Luedeke

Annette Arndt

Thomas J. Schnoeller

Jochen K. Lennerz

Carina Wurm

Christiane Maier

Marcus V. Cronauer

Konrad Steinestel

Andres J. Schrader

Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.
PII: 3925