@article{discovery10131513,
            note = {This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.},
           month = {July},
         journal = {British Journal of Cancer},
            year = {2021},
           title = {Molecular subtype-specific efficacy of anti-EGFR therapy in colorectal cancer is dependent on the chemotherapy backbone},
             url = {https://doi.org/10.1038/s41416-021-01477-9},
        abstract = {BACKGROUND: Patient selection for addition of anti-EGFR therapy to chemotherapy for patients with RAS and BRAF wildtype metastatic colorectal cancer can still be optimised. Here we investigate the effect of anti-EGFR therapy on survival in different consensus molecular subtypes (CMSs) and stratified by primary tumour location. METHODS: Retrospective analyses, using the immunohistochemistry-based CMS classifier, were performed in the COIN (first-line oxaliplatin backbone with or without cetuximab) and PICCOLO trial (second-line irinotecan with or without panitumumab). Tumour tissue was available for 323 patients (20\%) and 349 (41\%), respectively. RESULTS: When using an irinotecan backbone, anti-EGFR therapy is effective in both CMS2/3 and CMS4 in left-sided primary tumours (progression-free survival (PFS): HR 0.44, 95\% CI 0.26-0.75, P = 0.003 and HR 0.12, 95\% CI 0.04-0.36, P {\ensuremath{<}} 0.001, respectively) and in CMS4 right-sided tumours (PFS HR 0.17, 95\% CI 0.04-0.71, P = 0.02). Efficacy using an oxaliplatin backbone was restricted to left-sided CMS2/3 tumours (HR 0.57, 95\% CI 0.36-0.96, P = 0.034). CONCLUSIONS: The subtype-specific efficacy of anti-EGFR therapy is dependent on the chemotherapy backbone. This may provide the possibility of subtype-specific treatment strategies for a more optimal use of anti-EGFR therapy.},
          author = {Ten Hoorn, S and Sommeijer, DW and Elliott, F and Fisher, D and de Back, TR and Trinh, A and Koens, L and Maughan, T and Seligmann, J and Seymour, MT and Quirke, P and Adams, R and Richman, SD and Punt, CJA and Vermeulen, L},
        keywords = {Chemotherapy, Colorectal cancer, Metastasis}
}