Time From Colorectal Cancer Surgery to Adjuvant Chemotherapy: Post Hoc Analysis of the SCOT Randomized Clinical Trial.


Journal

JAMA surgery
ISSN: 2168-6262
Titre abrégé: JAMA Surg
Pays: United States
ID NLM: 101589553

Informations de publication

Date de publication:
12 Jun 2024
Historique:
medline: 12 6 2024
pubmed: 12 6 2024
entrez: 12 6 2024
Statut: aheadofprint

Résumé

The timing of adjuvant chemotherapy after surgery for colorectal cancer and its association with long-term outcomes have been investigated in national cohort studies, with no consensus on the optimal time from surgery to adjuvant chemotherapy. To analyze the association between the timing of adjuvant chemotherapy after surgery for colorectal cancer and disease-free survival. This is a post hoc analysis of the phase 3 SCOT randomized clinical trial, from 244 centers in 6 countries, investigating the noninferiority of 3 vs 6 months of adjuvant chemotherapy. Patients with high-risk stage II or stage III nonmetastatic colorectal cancer who underwent curative-intended surgery were randomized to either 3 or 6 months of adjuvant chemotherapy consisting of fluoropyrimidine and oxaliplatin regimens. Those with complete information on the date of surgery, treatment type, and long-term follow-up were investigated for the primary and secondary end points. Data were analyzed from May 2022 to February 2024. In the post hoc analysis, patients were grouped according to the start of adjuvant chemotherapy being less than 6 weeks vs greater than 6 weeks after surgery. The primary end point was disease-free survival. The secondary end points were adverse events in the total treatment period or the first cycle of adjuvant chemotherapy. A total of 5719 patients (2251 [39.4%] female; mean [SD] age, 63.4 [9.3] years) were included in the primary analysis after data curation; among them, 914 were in the early-start group and 4805 were in the late-start group. Median (IQR) follow-up was 72.0 (47.3-88.1) months, with a median (IQR) of 56 (41-66) days from surgery to chemotherapy. Five-year disease-free survival was 78.0% (95% CI, 75.3%-80.8%) in the early-start group and 73.2% (95% CI, 72.0%-74.5%) in the late-start group. In an adjusted Cox regression analysis, the start of adjuvant chemotherapy greater than 6 weeks after surgery was associated with worse disease-free survival (hazard ratio, 1.24; 95% CI, 1.06-1.46; P = .01). In adjusted logistic regression models, there was no association with adverse events in the total treatment period (odds ratio, 0.82; 95% CI, 0.65-1.04; P = .09) or adverse events in the first cycle of treatment (odds ratio, 0.77; 95% CI, 0.56-1.09; P = .13). In this international population of patients with high-risk stage II and stage III colorectal cancer, starting adjuvant chemotherapy more than 6 weeks after surgery was associated with worse disease-free survival, with no difference in adverse events between the groups. isrctn.org Identifier: ISRCTN59757862.

Identifiants

pubmed: 38865139
pii: 2820077
doi: 10.1001/jamasurg.2024.1555
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Mikail Gögenur (M)

Center for Surgical Science, Department of Surgery, Zealand University Hospital, Køge, Denmark.

Andreas Weinberger Rosen (AW)

Center for Surgical Science, Department of Surgery, Zealand University Hospital, Køge, Denmark.

Timothy Iveson (T)

Southampton University, Southampton, United Kingdom.

Rachel S Kerr (RS)

Department of Oncology, University of Oxford, Oxford, United Kingdom.

Mark P Saunders (MP)

The Christie Hospital, Manchester, United Kingdom.

Jim Cassidy (J)

Glasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.

Josep Tabernero (J)

Vall d'Hebron University Hospital and Institute of Oncology, Universitat Autònoma de Barcelona, Centro de Investigación Biomédica en Red de Cáncer, Barcelona, Spain.

Andrew Haydon (A)

Australasian Gastro-Intestinal Trials Group, Sydney, Australia.

Bengt Glimelius (B)

Department of Immunology, Genetics and Pathology, University of Uppsala, Uppsala, Sweden.

Andrea Harkin (A)

Glasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.

Karen Allan (K)

Glasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.

Sarah Pearson (S)

Oncology Clinical Trials Office, Department of Oncology, University of Oxford, Oxford, United Kingdom.

Kathleen A Boyd (KA)

School of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom.

Andrew H Briggs (AH)

School of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom.
London School of Hygiene and Tropical Medicine, London, United Kingdom.

Ashita Waterston (A)

Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.

Louise Medley (L)

Royal United Hospital, Bath, United Kingdom.

Richard Ellis (R)

Royal Cornwall Hospitals, National Health Service Trust, Cornwall, United Kingdom.

Amandeep S Dhadda (AS)

Castle Hill Hospital, Hull, United Kingdom.

Mark Harrison (M)

Mount Vernon Cancer Centre, Northwood, United Kingdom.

Stephen Falk (S)

Bristol Cancer Institute, Bristol, United Kingdom.

Charlotte Rees (C)

Southampton University, Southampton, United Kingdom.

Rene K Olesen (RK)

Department of Oncology, Aalborg University Hospital, Aalborg, Denmark.

David Propper (D)

Southampton University, Southampton, United Kingdom.
Barts Cancer Institute, Queen Mary, University of London, London, United Kingdom.

John Bridgewater (J)

University College London, London, United Kingdom.

Ashraf Azzabi (A)

Newcastle upon Tyne Hospitals, National Health Service Foundation Trust, Newcastle, United Kingdom.

David Cunningham (D)

Brighton and Sussex University Hospital Trust, Brighton, United Kingdom.

Tamas Hickish (T)

University Hospitals Dorset, Bournemouth University, Bournemouth, United Kingdom.

Simon Gollins (S)

North Wales Cancer Treatment Centre, Rhyl, United Kingdom.

Harpreet S Wasan (HS)

Hammersmith Hospital, Imperial College London, London, United Kingdom.

Caroline Kelly (C)

Glasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.

Ismail Gögenur (I)

Center for Surgical Science, Department of Surgery, Zealand University Hospital, Køge, Denmark.
Danish Colorectal Cancer Group, Copenhagen, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Niels Henrik Holländer (NH)

Department of Clinical Oncology and Palliative Care, Zealand University Hospital, Køge, Denmark.

Classifications MeSH