Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Clinical Oncology 2020
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
_version_ 1783589453661470720
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
work_keys_str_mv AT fontanaelisa intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT nyamundandagift intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT cunninghamdavid intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT tudongsheng intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT cheangmaggiecu intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT jonkerderekj intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT siulillianl intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT sclafanifrancesco intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT easonkatherine intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT ragulanchanthirika intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT balimariaantonietta intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT hulkkiwilsonsanna intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT loreejonathanm intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT waringpaulm intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT giordanomirella intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT lawrencepatrick intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT rodriguesdanielnava intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT begumruwaida intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT shapirojeremyd intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT pricetimothyj intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT cremolinichiara intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT starlingnaureen intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT pietrantoniofilippo intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT trusolinolivio intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT ocallaghanchristopherj intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial
AT sadanandamanguraj intratumoraltranscriptomeheterogeneityisassociatedwithpatientprognosisandsidednessinpatientswithcolorectalcancertreatedwithantiegfrtherapyfromtheco20trial