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Validation of a Metastatic Assay using biopsies to improve risk stratification in patients with prostate cancer treated with radical radiation therapy.
Jain, S; Lyons, C A; Walker, S M; McQuaid, S; Hynes, S O; Mitchell, D M; Pang, B; Logan, G E; McCavigan, A M; O'Rourke, D; McArt, D G; McDade, S S; Mills, I G; Prise, K M; Knight, L A; Steele, C J; Medlow, P W; Berge, V; Katz, B; Loblaw, D A; Harkin, D P; James, J A; O'Sullivan, J M; Kennedy, R D; Waugh, D J.
Affiliation
  • Jain S; Centre for Cancer Research & Cell Biology, Queen's University Belfast, Belfast, UK.
  • Lyons CA; Centre for Cancer Research & Cell Biology, Queen's University Belfast, Belfast, UK.
  • Walker SM; Centre for Cancer Research & Cell Biology, Queen's University Belfast, Belfast, UK.
  • McQuaid S; Almac Diagnostics, Seagoe Industrial Estate, Craigavon, UK.
  • Hynes SO; Centre for Cancer Research & Cell Biology, Queen's University Belfast, Belfast, UK.
  • Mitchell DM; Department of Pathology, University Hospital Galway, Galway, Ireland.
  • Pang B; Northern Ireland Cancer Centre, Belfast City Hospital, Belfast, UK.
  • Logan GE; Department of Pathology, National University Cancer Institute, Singapore.
  • McCavigan AM; Almac Diagnostics, Seagoe Industrial Estate, Craigavon, UK.
  • O'Rourke D; Almac Diagnostics, Seagoe Industrial Estate, Craigavon, UK.
  • McArt DG; Department of Pathology, Belfast City Hospital, Belfast, UK.
  • McDade SS; Centre for Cancer Research & Cell Biology, Queen's University Belfast, Belfast, UK.
  • Mills IG; Centre for Cancer Research & Cell Biology, Queen's University Belfast, Belfast, UK.
  • Prise KM; Centre for Cancer Research & Cell Biology, Queen's University Belfast, Belfast, UK.
  • Knight LA; Centre for Cancer Research & Cell Biology, Queen's University Belfast, Belfast, UK.
  • Steele CJ; Centre for Cancer Research & Cell Biology, Queen's University Belfast, Belfast, UK.
  • Medlow PW; Almac Diagnostics, Seagoe Industrial Estate, Craigavon, UK.
  • Berge V; Almac Diagnostics, Seagoe Industrial Estate, Craigavon, UK.
  • Katz B; Almac Diagnostics, Seagoe Industrial Estate, Craigavon, UK.
  • Loblaw DA; Department of Urology, Oslo University Hospital, Oslo, Norway.
  • Harkin DP; Department of Urology, Oslo University Hospital, Oslo, Norway.
  • James JA; Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada.
  • O'Sullivan JM; Centre for Cancer Research & Cell Biology, Queen's University Belfast, Belfast, UK.
  • Kennedy RD; Almac Diagnostics, Seagoe Industrial Estate, Craigavon, UK.
  • Waugh DJ; Centre for Cancer Research & Cell Biology, Queen's University Belfast, Belfast, UK.
Ann Oncol ; 29(1): 215-222, 2018 01 01.
Article in En | MEDLINE | ID: mdl-29045551
ABSTRACT

Background:

Radiotherapy is an effective treatment of intermediate/high-risk locally advanced prostate cancer, however, >30% of patients relapse within 5 years. Clinicopathological parameters currently fail to identify patients prone to systemic relapse and those whom treatment intensification may be beneficial. The purpose of this study was to independently validate the performance of a 70-gene Metastatic Assay in a cohort of diagnostic biopsies from patients treated with radical radiotherapy and androgen deprivation therapy. Patients and

methods:

A bridging cohort of prostate cancer diagnostic biopsy specimens was profiled to enable optimization of the Metastatic Assay threshold before further independent clinical validation in a cohort of diagnostic biopsies from patients treated with radical radiotherapy and androgen deprivation therapy. Multivariable Cox proportional hazard regression analysis was used to assess assay performance in predicting biochemical failure-free survival (BFFS) and metastasis-free survival (MFS).

Results:

Gene expression analysis was carried out in 248 patients from the independent validation cohort and the Metastatic Assay applied. Ten-year MFS was 72% for Metastatic Assay positive patients and 94% for Metastatic Assay negative patients [HR = 3.21 (1.35-7.67); P = 0.003]. On multivariable analysis the Metastatic Assay remained predictive for development of distant metastases [HR = 2.71 (1.11-6.63); P = 0.030]. The assay retained independent prognostic performance for MFS when assessed with the Cancer of the Prostate Assessment Score (CAPRA) [HR = 3.23 (1.22-8.59); P = 0.019] whilst CAPRA itself was not significant [HR = 1.88, (0.52-6.77); P = 0.332]. A high concordance [100% (61.5-100)] for the assay result was noted between two separate foci taken from 11 tumours, whilst Gleason score had low concordance.

Conclusions:

The Metastatic Assay demonstrated significant prognostic performance in patients treated with radical radiotherapy both alone and independent of standard clinical and pathological variables. The Metastatic Assay could have clinical utility when deciding upon treatment intensification in high-risk patients. Genomic and clinical data are available as a public resource.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Biopsy Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Humans / Male / Middle aged Language: En Journal: Ann Oncol Journal subject: NEOPLASIAS Year: 2018 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Biopsy Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Humans / Male / Middle aged Language: En Journal: Ann Oncol Journal subject: NEOPLASIAS Year: 2018 Document type: Article Affiliation country: United kingdom