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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
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 cla...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Clinical Oncology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529528/ https://www.ncbi.nlm.nih.gov/pubmed/33015526 http://dx.doi.org/10.1200/PO.20.00050 |
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author | 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 |
author_facet | 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 |
author_sort | Fontana, Elisa |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7529528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society of Clinical Oncology |
record_format | MEDLINE/PubMed |
spelling | pubmed-75295282020-10-02 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 JCO Precis Oncol Original Reports 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. American Society of Clinical Oncology 2020-09-29 /pmc/articles/PMC7529528/ /pubmed/33015526 http://dx.doi.org/10.1200/PO.20.00050 Text en © 2020 by American Society of Clinical Oncology https://creativecommons.org/licenses/by/4.0/ Licensed under the Creative Commons Attribution 4.0 License: https://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Reports 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 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 |
title | 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 |
title_full | 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 |
title_fullStr | 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 |
title_full_unstemmed | 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 |
title_short | 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 |
title_sort | 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 |
topic | Original Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529528/ https://www.ncbi.nlm.nih.gov/pubmed/33015526 http://dx.doi.org/10.1200/PO.20.00050 |
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