Benefit of adjuvant chemotherapy on recurrence free survival per consensus molecular subtype in stage III colon cancer

Author:

van de Weerd Simone123,Torang Arezo13ORCID,van den Berg Inge45ORCID,Lammers Veerle13,van den Bergh Saskia13,Brouwer Nelleke2ORCID,Nagtegaal Iris D.2,Koopman Miriam5,Vink Geraldine R.56,van der Baan Frederieke H.5,van Krieken Han2,Koster Jan1,Ijzermans Jan N.4,Roodhart Jeanine M. L.5ORCID,Medema Jan Paul13

Affiliation:

1. Amsterdam UMC location University of Amsterdam Center for Experimental and Molecular Medicine, Cancer Center Amsterdam Amsterdam The Netherlands

2. Department of Pathology Radboud University Medical Center Nijmegen The Netherlands

3. Oncode Institute, Amsterdam UMC University of Amsterdam Amsterdam The Netherlands

4. Department of Surgery, Erasmus MC University Medical center Rotterdam Rotterdam The Netherlands

5. Department of Medical Oncology, University Medical Center Utrecht Utrecht University Utrecht The Netherlands

6. Department of Research and Development Netherlands Comprehensive Cancer Organisation Utrecht The Netherlands

Abstract

AbstractThe consensus molecular subtype (CMS) classification divides colon tumors into four subtypes holding promise as a predictive biomarker. However, the effect of adjuvant chemotherapy on recurrence free survival (RFS) per CMS in stage III patients remains inadequately explored. With this intention, we selected stage III colon cancer (CC) patients from the MATCH cohort (n = 575) and RadboudUMC (n = 276) diagnosed between 2005 and 2018. Patients treated with and without adjuvant chemotherapy were matched based on tumor location, T‐ and N‐stage (n = 522). Tumor material was available for 464 patients, with successful RNA extraction and CMS subtyping achieved in 390 patients (surgery alone group: 192, adjuvant chemotherapy group: 198). In the overall cohort, CMS4 was associated with poorest prognosis (HR 1.55; p = .03). Multivariate analysis revealed favorable RFS for the adjuvant chemotherapy group in CMS1, CMS2, and CMS4 tumors (HR 0.19; p = .01, HR 0.27; p < .01, HR 0.19; p < .01, respectively), while no significant difference between treatment groups was observed within CMS3 (HR 0.68; p = .51). CMS subtyping in this non‐randomized cohort identified patients with poor prognosis and patients who may not benefit significantly from adjuvant chemotherapy.

Funder

KWF Kankerbestrijding

Publisher

Wiley

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