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

Author:

Fontana Elisa12,Nyamundanda Gift12,Cunningham David3ORCID,Tu Dongsheng4ORCID,Cheang Maggie C.U.56ORCID,Jonker Derek J.7,Siu Lillian L.8,Sclafani Francesco39,Eason Katherine1ORCID,Ragulan Chanthirika12,Bali Maria Antonietta1011ORCID,Hulkki-Wilson Sanna1,Loree Jonathan M.12ORCID,Waring Paul M.13ORCID,Giordano Mirella14,Lawrence Patrick12,Rodrigues Daniel Nava3ORCID,Begum Ruwaida3,Shapiro Jeremy D.15,Price Timothy J.16,Cremolini Chiara1718ORCID,Starling Naureen3ORCID,Pietrantonio Filippo1920ORCID,Trusolino Livio2122ORCID,O’Callaghan Christopher J.4,Sadanandam Anguraj12ORCID

Affiliation:

1. Division of Molecular Pathology, The Institute of Cancer Research, London, United Kingdom

2. The Royal Marsden Hospital, London, United Kingdom

3. GI Cancer Unit, The Royal Marsden Hospital, London, United Kingdom

4. Canadian Clinical Trial Group, Kingston, Ontario, Canada

5. Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, United Kingdom

6. Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, United Kingdom

7. The Ottawa Hospital, Ottawa, Ontario, Canada

8. Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada

9. GI Cancer Unit, Institut Jules Bordet, Brussels, Belgium

10. Radiology Department, The Royal Marsden Hospital, London, United Kingdom

11. Radiology Department, Jules Bordet, Brussels, Belgium

12. BC Cancer, Vancouver, British Columbia, Canada

13. Department of Pathology, University of Melbourne, Melbourne, Victoria, Australia

14. Department of Surgical, Medical, Molecular Pathology, and Critical Area, University of Pisa, Pisa, Italy

15. Cabrini Health, Department of Medical Oncology, Malvern, Victoria, Australia

16. Queen Elizabeth Hospital, Adelaide, South Australia, Australia

17. Medical Oncology Unit, Azienda Ospedaliero‐Universitaria Pisana, Pisa, Italy

18. Department of Translational Research and New Technologies in Medicine, University of Pisa, Pisa, Italy

19. Medical Oncology Department, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico Istituto Nazionale dei Tumori, Milan, Italy

20. Oncology and Hemato-Oncology Department, Milan University, Milan, Italy

21. Department of Oncology, University of Torino Medical School, Candiolo, Torino, Italy

22. Translational Cancer Medicine, Candiolo Cancer Institute, FPO IRCCS, Candiolo, Torino, Italy

Abstract

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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3