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Phase 2 study of circulating microRNA biomarkers in castration-resistant prostate cancer.
Lin, Hui-Ming; Mahon, Kate L; Spielman, Calan; Gurney, Howard; Mallesara, Girish; Stockler, Martin R; Bastick, Patricia; Briscoe, Karen; Marx, Gavin; Swarbrick, Alexander; Horvath, Lisa G.
  • Lin HM; Cancer Division, The Kinghorn Cancer Centre/Garvan Institute of Medical Research, Darlinghurst, New South Wales 2010, Australia.
  • Mahon KL; St Vincent's Clinical School, Faculty of Medicine, The University of New South Wales, Darlinghurst, New South Wales 2010, Australia.
  • Spielman C; Cancer Division, The Kinghorn Cancer Centre/Garvan Institute of Medical Research, Darlinghurst, New South Wales 2010, Australia.
  • Gurney H; St Vincent's Clinical School, Faculty of Medicine, The University of New South Wales, Darlinghurst, New South Wales 2010, Australia.
  • Mallesara G; Department of Medical Oncology, Chris O'Brien Lifehouse, Camperdown, New South Wales 2050, Australia.
  • Stockler MR; Royal Prince Alfred Hospital, Camperdown, New South Wales 2050, Australia.
  • Bastick P; Cancer Division, The Kinghorn Cancer Centre/Garvan Institute of Medical Research, Darlinghurst, New South Wales 2010, Australia.
  • Briscoe K; Crown Princess Mary Cancer Centre, Westmead Hospital, Westmead, New South Wales 2145, Australia.
  • Marx G; Pharmacogenomics Research for Individualised Medicine (PRIMe) consortium, New South Wales, Australia.
  • Swarbrick A; Pharmacogenomics Research for Individualised Medicine (PRIMe) consortium, New South Wales, Australia.
  • Horvath LG; Calvary Mater Newcastle Hospital, Waratah, New South Wales 2298, Australia.
Br J Cancer ; 116(8): 1002-1011, 2017 Apr 11.
Article en En | MEDLINE | ID: mdl-28278515
ABSTRACT

BACKGROUND:

Biomarkers of therapeutic response and prognosis are needed to assist in the sequencing of treatments for metastatic castration-resistant prostate cancer (CRPC). Previously in a Phase 1 discovery study, we identified 14 circulating microRNAs that were associated with response to docetaxel chemotherapy or overall survival. We performed a Phase 2 validation study to verify these findings.

METHODS:

Using real-time PCR, the levels of the 14 microRNAs were measured in plasma collected before and after the first cycle of docetaxel from a Phase 2 cohort of 89 patients.

RESULTS:

The microRNAs were not associated with docetaxel response in the Phase 2 cohort. Higher baseline levels of six microRNAs, predominantly of the miR-200 family, were confirmed to be associated with shorter overall survival. A microRNA signature comprising these six microRNAs predicted high-risk patients in the Phase 2 cohort with a hazard ratio of 4.12 (95% CI 2.20-7.70, P=0.000001). The signature was an independent predictor in multivariable analysis with clinicopathological factors.

CONCLUSIONS:

The association of circulating microRNAs with overall survival suggests their involvement in CRPC progression.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biomarcadores de Tumor / MicroARNs / Taxoides / Neoplasias de la Próstata Resistentes a la Castración / Antineoplásicos Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biomarcadores de Tumor / MicroARNs / Taxoides / Neoplasias de la Próstata Resistentes a la Castración / Antineoplásicos Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article