Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

2422 - Role of AR-V7 and AR-FL in resistance to hormonal therapy in mCRPC: independent actors or reciprocal drivers? A translational study by Meet-Uro group

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Topics

Tumour Site

Prostate Cancer

Presenters

Marzia Del Re

Citation

Annals of Oncology (2018) 29 (suppl_8): viii14-viii57. 10.1093/annonc/mdy269

Authors

M. Del Re1, S. Crucitta2, A. Sbrana3, E. Rofi2, F. Paolieri4, L. Galli5, A. Falcone4, R. van Schaik6, G. Jenster7, R. Morganti3, S. Pignata8, R. Danesi1

Author affiliations

  • 1 Clinical And Experimental Medicine, University of Pisa, 56126 - Pisa/IT
  • 2 Clinical And Experimental Medicine, University of Pisa, 56100 - Pisa/IT
  • 3 Medical Oncology 2 Unit, Azienda Ospedaliera Universitaria S.Chiara, 56100 - Pisa/IT
  • 4 Medical Oncology, Azienda Ospedaliera Universitaria S.Chiara, 56100 - Pisa/IT
  • 5 Uo Oncologia Medica 2 Universitaria, Azienda Ospedaliero-Universitaria Pisana Istituto Toscano Tumori, 56100 - Pisa/IT
  • 6 Clinical Chemistry, Erasmus University, Rotterdam/NL
  • 7 Josephine Nefkens Institute, Erasmus University, Rotterdam/NL
  • 8 Urology And Gynecology, Istituto Nazionale Tumori – I.R.C.C.S - Fondazione Pascale, 80131 - Napoli/IT

Resources

Login to access the resources on OncologyPRO.

If you do not have an ESMO account, please create one for free.

Abstract 2422

Background

The androgen receptor splice variant 7 (AR-V7) is strongly associated with resistance to hormonal therapy (HT) in castration-resistant prostate cancer (CRPC), although it is not implemented in clinical practice as a biomarker. The AR-full length (AR-FL) is also overexpressed in CRPC but its role has yet to be clarified. The aim of the present work was to investigate the role of AR-V7 and AR-FL as predictors of resistance to HT in plasma-derived exosomal RNA.

Methods

6 ml of blood were collected in EDTA tubes before the start of abiraterone/enzalutamide; blood was centrifuged and plasma stored at -80 °C until analysis. Exosomes isolation and RNA extraction were performed using the exoRNeasy kit (Qiagen) as per manufacturer instructions. The analysis of AR-FL and AR-V7 were performed by digital droplet PCR using the One-Step RT-ddPCR kit (BioRad). The absolute target concentration as copies/ml in samples was calculated by ddPCR QuantaSoft and statistical analyses were performed by SPSS v.24.

Results

52 patients (pts) were enrolled; AR-FL was detected in all pts (median: 700 copies/ml), while 15 subjects (28.8%) were AR-V7 + (median: 310 copies/ml) at baseline. The amount of AR-FL was significantly higher in pts AR-V7+ vs AR-V7- (6700 vs 490 copies/ml, p < 0.0001). Median PFS and OS were longer in AR-V7- vs AR-V7+ pts (median PFS 25 vs 4 mo, p < 0.0001; median OS 38 vs 9 mo, p < 0.0001). A ROC curve was calculated for AR-FL in the overall population and 950 copies/ml was identified as cut-off value. Pts were then stratified across this value and it was found that PFS was 22 mo in pts with <950 AR-FL copies/ml vs 4 mo in pts with ≥950 copies/ml (p = 0.0003). In 12/15 AR-V7+ pts the AR-FL expression was ≥950 copies/ml while in 3/15 AR-V7+ pts, AR-FL expression was <950 copies/ml; however, their PFS reflected the AR-V7 better than AR-FL status, being, respectively 6, 10, 4 mo. No other clinical variables were correlated with worse PFS at the univariate analysis (i.e. Gleason score ≤7 vs > 7, age).

Conclusions

This study demonstrates that resistance to HT may be predicted by AR-V7, making it a clinically relevant biomarker. AR-FL over-expression may contribute to hormone resistance although AR-V7 plays a primary role.

Clinical trial identification

Legal entity responsible for the study

Romano Danesi.

Funding

University of Pisa.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.