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Intratumoral Transcriptome Heterogeneity Is Associated With Patient Prognosis and Sidedness in Patients With Colorectal Cancer Treated With Anti-EGFR Therapy From the CO.20 Trial.
Fontana, Elisa; Nyamundanda, Gift; Cunningham, David; Tu, Dongsheng; Cheang, Maggie C U; Jonker, Derek J; Siu, Lillian L; Sclafani, Francesco; Eason, Katherine; Ragulan, Chanthirika; Bali, Maria Antonietta; Hulkki-Wilson, Sanna; Loree, Jonathan M; Waring, Paul M; Giordano, Mirella; Lawrence, Patrick; Rodrigues, Daniel Nava; Begum, Ruwaida; Shapiro, Jeremy D; Price, Timothy J; Cremolini, Chiara; Starling, Naureen; Pietrantonio, Filippo; Trusolino, Livio; O'Callaghan, Christopher J; Sadanandam, Anguraj.
Affiliation
  • Fontana E; Division of Molecular Pathology, The Institute of Cancer Research, London, United Kingdom.
  • Nyamundanda G; The Royal Marsden Hospital, London, United Kingdom.
  • Cunningham D; Division of Molecular Pathology, The Institute of Cancer Research, London, United Kingdom.
  • Tu D; The Royal Marsden Hospital, London, United Kingdom.
  • Cheang MCU; GI Cancer Unit, The Royal Marsden Hospital, London, United Kingdom.
  • Jonker DJ; Canadian Clinical Trial Group, Kingston, Ontario, Canada.
  • Siu LL; Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, United Kingdom.
  • Sclafani F; Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, United Kingdom.
  • Eason K; The Ottawa Hospital, Ottawa, Ontario, Canada.
  • Ragulan C; Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
  • Bali MA; GI Cancer Unit, The Royal Marsden Hospital, London, United Kingdom.
  • Hulkki-Wilson S; GI Cancer Unit, Institut Jules Bordet, Brussels, Belgium.
  • Loree JM; Division of Molecular Pathology, The Institute of Cancer Research, London, United Kingdom.
  • Waring PM; Division of Molecular Pathology, The Institute of Cancer Research, London, United Kingdom.
  • Giordano M; The Royal Marsden Hospital, London, United Kingdom.
  • Lawrence P; Radiology Department, The Royal Marsden Hospital, London, United Kingdom.
  • Rodrigues DN; Radiology Department, Jules Bordet, Brussels, Belgium.
  • Begum R; Division of Molecular Pathology, The Institute of Cancer Research, London, United Kingdom.
  • Shapiro JD; BC Cancer, Vancouver, British Columbia, Canada.
  • Price TJ; Department of Pathology, University of Melbourne, Melbourne, Victoria, Australia.
  • Cremolini C; Department of Surgical, Medical, Molecular Pathology, and Critical Area, University of Pisa, Pisa, Italy.
  • Starling N; Division of Molecular Pathology, The Institute of Cancer Research, London, United Kingdom.
  • Pietrantonio F; The Royal Marsden Hospital, London, United Kingdom.
  • Trusolino L; GI Cancer Unit, The Royal Marsden Hospital, London, United Kingdom.
  • O'Callaghan CJ; GI Cancer Unit, The Royal Marsden Hospital, London, United Kingdom.
  • Sadanandam A; Cabrini Health, Department of Medical Oncology, Malvern, Victoria, Australia.
Article in En | MEDLINE | ID: mdl-33015526
PURPOSE: Metastatic colorectal cancers (mCRCs) assigned to the transit-amplifying (TA) CRCAssigner subtype are more sensitive to anti-epidermal growth factor receptor (EGFR) therapy. We evaluated the association between the intratumoral presence of TA signature (TA-high/TA-low, dubbed as TA-ness classification) and outcomes in CRCs treated with anti-EGFR therapy. PATIENTS AND METHODS: The TA-ness classes were defined in a discovery cohort (n = 84) and independently validated in a clinical trial (CO.20; cetuximab monotherapy arm; n = 121) and other samples using an established NanoString-based gene expression assay. Progression-free survival (PFS), overall survival (OS), and disease control rate (DCR) according to TA-ness classification were assessed by univariate and multivariate analyses. RESULTS: The TA-ness was measured in 772 samples from 712 patients. Patients (treated with anti-EGFR therapy) with TA-high tumors had significantly longer PFS (discovery hazard ratio [HR], 0.40; 95% CI, 0.25 to 0.64; P < .001; validation HR, 0.65; 95% CI, 0.45 to 0.93; P = .018), longer OS (discovery HR, 0.48; 95% CI, 0.29 to 0.78; P = .003; validation HR, 0.67; 95% CI, 0.46 to 0.98; P = .04), and higher DCR (discovery odds ratio [OR]; 14.8; 95% CI, 4.30 to 59.54; P < .001; validation OR, 4.35; 95% CI, 2.00 to 9.09; P < .001). TA-ness classification and its association with anti-EGFR therapy outcomes were further confirmed using publicly available data (n = 80) from metastatic samples (PFS P < .001) and patient-derived xenografts (P = .042). In an exploratory analysis of 55 patients with RAS/BRAF wild-type and left-sided tumors, TA-high class was significantly associated with longer PFS and trend toward higher response rate (PFS HR, 0.53; 95% CI, 0.28 to 1.00; P = .049; OR, 5.88; 95% CI, 0.71 to 4.55; P = .09; response rate 33% in TA-high and 7.7% in TA-low). CONCLUSION: TA-ness classification is associated with prognosis in patients with mCRC treated with anti-EGFR therapy and may further help understanding the value of sidedness in patients with RAS/BRAF wild-type tumors.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Language: En Journal: JCO Precis Oncol Year: 2020 Document type: Article Affiliation country: Reino Unido Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Language: En Journal: JCO Precis Oncol Year: 2020 Document type: Article Affiliation country: Reino Unido Country of publication: Estados Unidos