4.7 Article

Prognostic value of the 6-gene OncoMasTR test in hormone receptor-positive HER2-negative early-stage breast cancer: Comparative analysis with standard clinicopathological factors

Journal

EUROPEAN JOURNAL OF CANCER
Volume 152, Issue -, Pages 78-89

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.ejca.2021.04.016

Keywords

Breast cancer; ER thorn; HER2; Prognostic biomarker; Recurrence score

Categories

Funding

  1. European Union's Horizon 2020 research and innovation programme [698630]
  2. Irish Cancer Society Collaborative Cancer Research Centre BREAST-PREDICT [CCRC13GAL]
  3. Science Foundation Ireland (SFI) under the Investigator Programme OPTi-PREDICT [15/IA/3104]
  4. Strategic Research Programme Precision Oncology Ireland [18/SPP/3522]
  5. SFI [18/SPP/3522, 12TIDAB2436]
  6. SFI Career Development Award [15/CDA/3438]
  7. H2020 Societal Challenges Programme [698630] Funding Source: H2020 Societal Challenges Programme
  8. Science Foundation Ireland (SFI) [15/CDA/3438] Funding Source: Science Foundation Ireland (SFI)

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The study assessed the prognostic performance of a 6-gene molecular score and a composite risk score against four routinely used molecular and clinicopathological risk assessment tools. Results showed that both scores were significantly prognostic for distant recurrence-free survival and invasive disease-free survival, providing additional prognostic information to other risk factors/tools assessed. The 6-gene signature demonstrated superior risk stratification and increased prognosis reliability for treatment decisions.
Aim: The aim of the study was to assess the prognostic performance of a 6-gene molecular score (OncoMasTR Molecular Score [OMm]) and a composite risk score (OncoMasTR Risk Score [OM]) and to conduct a within-patient comparison against four routinely used molecular and clinicopathological risk assessment tools: Oncotype DX Recurrence Score, Ki67, Nottingham Prognostic Index and Clinical Risk Category, based on the modified Adjuvant! Online definition and three risk factors: patient age, tumour size and grade. Methods: Biospecimens and clinicopathological information for 404 Irish women also previously enrolled in the Trial Assigning Individualized Options for Treatment [Rx] were provided by 11 participating hospitals, as the primary objective of an independent translational study. Gene expression measured via RT-qPCR was used to calculate OMm and OM. The prognostic value for distant recurrence-free survival (DRFS) and invasive disease-free survival (IDFS) was assessed using Cox proportional hazards models and Kaplan-Meier analysis. All statistical tests were two-sided ones. Results: OMm and OM (both with likelihood ratio statistic [LRS] P < 0.001; C indexes Z 0.84 and 0.85, respectively) were more prognostic for DRFS and provided significant additional prognostic information to all other assessment tools/factors assessed (all LRS P < 0.002). In addition, the OM correctly classified more patients with distant recurrences (DRs) into the high-risk category than other risk classification tools. Similar results were observed for IDFS. Discussion: Both OncoMasTR scores were significantly prognostic for DRFS and IDFS and provided additional prognostic information to the molecular and clinicopathological risk factors/tools assessed. OM was also the most accurate risk classification tool for identifying DR. A concise 6-gene signature with superior risk stratification was shown to increase prognosis reliability, which may help clinicians optimise treatment decisions. (c) 2021 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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