Time to recurrence and its relation to survival after recurrence in patients resected for stage III colon cancer.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
11 2023
Historique:
received: 25 06 2023
revised: 22 08 2023
accepted: 26 08 2023
medline: 27 11 2023
pubmed: 6 10 2023
entrez: 5 10 2023
Statut: ppublish

Résumé

It is intuitively thought that early relapse is associated with poor survival after recurrence (SAR) in resected colon cancer (CC) patients, but this has never been formally studied. We pooled data from stage III patients treated with oxaliplatin-based adjuvant therapy in two phase III trials, to analyse time to recurrence (TTR) and its relationship with SAR. TTR and SAR were also studied according to molecular status (mismatch repair (MMR), RAS, and BRAF 4548 stage III CC patients were included in the present analysis. Deficient MMR (dMMR) CC patients experienced fewer recurrences than proficient (p)MMR CC patients (18.8% versus 27.6%) but had a significantly shorter median TTR (mTTR; 0.74 versus 1.40 years, p < 0.0001). In pMMR patients, BRAF and RAS mutations were also associated with earlier mTTR as compared to double wild-type (WT) patients (0.99 versus 1.38 versus 1.54 years, respectively, p < 0.0001). Early recurrence occurred in 397 patients and was associated with a median SAR (2.2 versus 3.3 years, p = 0.0007). However, this association was mainly due to pMMR/RAS and BRAF In resected stage III CC treated with standard oxaliplatin-based adjuvant therapy, TTR varies between dMMR, pMMR/RAS, or BRAF

Sections du résumé

BACKGROUND
It is intuitively thought that early relapse is associated with poor survival after recurrence (SAR) in resected colon cancer (CC) patients, but this has never been formally studied.
METHODS
We pooled data from stage III patients treated with oxaliplatin-based adjuvant therapy in two phase III trials, to analyse time to recurrence (TTR) and its relationship with SAR. TTR and SAR were also studied according to molecular status (mismatch repair (MMR), RAS, and BRAF
RESULTS
4548 stage III CC patients were included in the present analysis. Deficient MMR (dMMR) CC patients experienced fewer recurrences than proficient (p)MMR CC patients (18.8% versus 27.6%) but had a significantly shorter median TTR (mTTR; 0.74 versus 1.40 years, p < 0.0001). In pMMR patients, BRAF and RAS mutations were also associated with earlier mTTR as compared to double wild-type (WT) patients (0.99 versus 1.38 versus 1.54 years, respectively, p < 0.0001). Early recurrence occurred in 397 patients and was associated with a median SAR (2.2 versus 3.3 years, p = 0.0007). However, this association was mainly due to pMMR/RAS and BRAF
CONCLUSION
In resected stage III CC treated with standard oxaliplatin-based adjuvant therapy, TTR varies between dMMR, pMMR/RAS, or BRAF

Identifiants

pubmed: 37797388
pii: S0959-8049(23)00623-8
doi: 10.1016/j.ejca.2023.113321
pii:
doi:

Substances chimiques

Proto-Oncogene Proteins B-raf EC 2.7.11.1
Oxaliplatin 04ZR38536J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113321

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest JT has received honoraria as a speaker or in an advisory role from Sanofi, Roche, Merck Serono, Amgen, Servier, Pierre Fabre, Lilly, AstraZeneca, and MSD. PLP has received honoraria as a speaker or in an advisory role from ESMO, Amgen, Servier, Pierre Fabre, Biocartis, and stocks from Methys DX. SL has received honoraria as an invited speaker from Roche, Eli Lilly, Bristol Myers Squibb, Servier, Merck Serono, Pierre Fabre, GlaxoSmithKline, Amgen, and has participated in an advisory board for Amgen, Merck Serono, Eli Lilly, AstraZeneca, Incyte, Daiichi-Sankyo, Bristol Myers Squibb, Servier, and Merck Sharp & Dohme. TA has attended advisory board meetings and received consulting fees from AstraZeneca, Astellas, Aptitude Health, Bristol Myers Squibb, Gritstone Oncology, GamaMabs Pharma SA, Gilead, GlaxoSmithKline, Merck & Co. Inc., Nordic Oncology, Pierre Fabre, Seagen, Servier and Transgene; has received honoraria from AstraZeneca, Bristol Myers Squibb, GlaxoSmithKline, Merck & Co. Inc., Merck Serono, Pierre Fabre, Roche, Sanofi, Seagen and Servier; and has received support for meetings from Merck & Co. Inc., and Servier. CL was a consultant and had an advisory role for Novartis and AAA, and has received speaker honoraria from AMGEN, and Bayer. OB has received honoraria as a speaker and in an advisory role from Merck Serono, Amgen, Bayer, Servier, Pierre Fabre, Deciphera, Apmonia Therapeutics, and MSD. AL has received honoraria as a consultant and speaker from Advance Accelerator Applications, Amgen, Bayer, F. Hofmann-La Roche, Incyte Corporation, Ipsen Biopharmaceuticals Inc, Mylan Pharmaceuticals Inc, Novartis, Pierre Fabre Pharmaceuticals Inc, Sandoz, Sanofi Pasteur Inc and has received research grants from Bayer and Lilly Deutschland. CLO reports personal fees and non-financial support from Merck, Roche; personal fees from Servier; and personal fees from Amgen outside the submitted work. JBB has received personal fees from Amgen, Bayer, Bristol Myers Squibb, Merck Serono, Merck Sharp & Dohme, Pierre Fabre, Sanofi, Servier, and non-financial support from Amgen, Merck Serono, and Roche, outside the submitted work. JB is involved as an advisory board member for AstraZeneca, Bristol-Myers Squibb, MSD, Novartis, Ipsen, Servier, and Sanofi and has received honoraria from AstraZeneca, Bayer, Bristol Myers Squibb, Merck, MSD, Daiichi, Servier, Ipsen, Jansen, and Sanofi. CB has received honoraria as a consultant from Bayer, Molecular Partners, MSD, Pierre Fabre, and Servier, and has received research grants from Bayer, Roche, and Boehringer. All remaining authors have declared no conflicts of interest.

Auteurs

Cosimo Rasola (C)

Department of Gastroenterology and GI Oncology, Georges Pompidou European Hospital, SIRIC CARPEM, Université Paris-Cité, Paris, France; Department of Oncology, Veneto Institute of Oncology IRCCS, Padua, Italy; Medical Oncology 3, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy; Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy.

Pierre Laurent-Puig (P)

Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université de Paris Cité, team Personalized Medicine, Phamacogenomics and Therapeutic Optimization, Paris, France; Institut du Cancer Paris CARPEM, AP-HP,Centre Department of Gastroenterology and Digestive Oncology, Hôpital Européen Georges Pompidou, Paris, France.

Thierry André (T)

Sorbonne Université and Medical Oncology Department, Hôpital Saint-Antoine, Paris, France.

Antoine Falcoz (A)

University Hospital of Besançon, Methodology and Quality of Life Unit in Oncology, Besançon, France; INSERM, Établissement Français du Sang Bourgogne Franche-Comté, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, Besançon, France.

Come Lepage (C)

Gastroenterology and Digestive Oncology, Hôpital Universitaire Le Bocage, Dijon, France.

Thomas Aparicio (T)

Université Paris-Cité, Gastroenterology Department, Hôpital Saint Louis, APHP, Paris, France.

Olivier Bouché (O)

Dept of Digestive Oncology, CHU Reims, Reims, France.

Astrid Lievre (A)

Digestive Unit, Hôpital Universitaire de Pontchaillou, Rennes, France.

Laurent Mineur (L)

Oncology Department, Clinique Sainte-Catherine, Avignon, France.

Jaafar Bennouna (J)

Department of Medical Oncology, Hôpital Foch, Suresnes, France.

Christophe Louvet (C)

Department of Medical Oncology, Institute Mutualiste Montsouris, Paris, France.

Jean Baptiste Bachet (JB)

Sorbonne University, Hepatogastroenterology and Digestive Oncology Department, Pitié Salpêtrière hospital, APHP, Paris, France.

Christophe Borg (C)

Department of Medical Oncology, University Hospital of Besançon, France.

Dewi Vernerey (D)

University Hospital of Besançon, Methodology and Quality of Life Unit in Oncology, Besançon, France; INSERM, Établissement Français du Sang Bourgogne Franche-Comté, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, Besançon, France.

Sara Lonardi (S)

Department of Oncology, Veneto Institute of Oncology IRCCS, Padua, Italy; Medical Oncology 3, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.

Julien Taieb (J)

Department of Gastroenterology and GI Oncology, Georges Pompidou European Hospital, SIRIC CARPEM, Université Paris-Cité, Paris, France. Electronic address: jtaieb75@gmail.com.

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