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Prospective patient stratification into robust cancer-cell intrinsic subtypes from colorectal cancer biopsies.
Alderdice, Matthew; Richman, Susan D; Gollins, Simon; Stewart, James P; Hurt, Chris; Adams, Richard; McCorry, Amy Mb; Roddy, Aideen C; Vimalachandran, Dale; Isella, Claudio; Medico, Enzo; Maughan, Tim; McArt, Darragh G; Lawler, Mark; Dunne, Philip D.
Afiliação
  • Alderdice M; Centre for Cancer Research and Cell Biology, Queens's University Belfast, Belfast, UK.
  • Richman SD; Department of Pathology and Tumour Biology, Leeds Institute of Cancer and Pathology, St James Hospital, Leeds, UK.
  • Gollins S; North Wales Cancer Treatment Centre, Rhyl, UK.
  • Stewart JP; Centre for Cancer Research and Cell Biology, Queens's University Belfast, Belfast, UK.
  • Hurt C; Centre for Trials Research, Cardiff University, Cardiff, UK.
  • Adams R; Centre for Trials Research, Cardiff University, Cardiff, UK.
  • McCorry AM; Centre for Cancer Research and Cell Biology, Queens's University Belfast, Belfast, UK.
  • Roddy AC; Centre for Cancer Research and Cell Biology, Queens's University Belfast, Belfast, UK.
  • Vimalachandran D; Countess of Chester Hospital, Chester, UK.
  • Isella C; University of Torino, Department of Oncology, Candiolo, Torino, Italy.
  • Medico E; Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.
  • Maughan T; University of Torino, Department of Oncology, Candiolo, Torino, Italy.
  • McArt DG; Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.
  • Lawler M; CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, UK.
  • Dunne PD; Centre for Cancer Research and Cell Biology, Queens's University Belfast, Belfast, UK.
J Pathol ; 245(1): 19-28, 2018 05.
Article em En | MEDLINE | ID: mdl-29412457
ABSTRACT
Colorectal cancer (CRC) biopsies underpin accurate diagnosis, but are also relevant for patient stratification in molecularly-guided clinical trials. The consensus molecular subtypes (CMSs) and colorectal cancer intrinsic subtypes (CRISs) transcriptional signatures have potential clinical utility for improving prognostic/predictive patient assignment. However, their ability to provide robust classification, particularly in pretreatment biopsies from multiple regions or at different time points, remains untested. In this study, we undertook a comprehensive assessment of the robustness of CRC transcriptional signatures, including CRIS and CMS, using a range of tumour sampling methodologies currently employed in clinical and translational research. These include analyses using (i) laser-capture microdissected CRC tissue, (ii) eight publically available rectal cancer biopsy data sets (n = 543), (iii) serial biopsies (from AXEBeam trial, NCT00828672; n = 10), (iv) multi-regional biopsies from colon tumours (n = 29 biopsies, n = 7 tumours), and (v) pretreatment biopsies from the phase II rectal cancer trial COPERNCIUS (NCT01263171; n = 44). Compared to previous results obtained using CRC resection material, we demonstrate that CMS classification in biopsy tissue is significantly less capable of reliably classifying patient subtype (43% unknown in biopsy versus 13% unknown in resections, p = 0.0001). In contrast, there was no significant difference in classification rate between biopsies and resections when using the CRIS classifier. Additionally, we demonstrated that CRIS provides significantly better spatially- and temporally- robust classification of molecular subtypes in CRC primary tumour tissue compared to CMS (p = 0.003 and p = 0.02, respectively). These findings have potential to inform ongoing biopsy-based patient stratification in CRC, enabling robust and stable assignment of patients into clinically-informative arms of prospective multi-arm, multi-stage clinical trials. © 2018 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biópsia / Neoplasias Colorretais / Regulação Neoplásica da Expressão Gênica / Neoplasias do Colo Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biópsia / Neoplasias Colorretais / Regulação Neoplásica da Expressão Gênica / Neoplasias do Colo Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article