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Time From Colorectal Cancer Surgery to Adjuvant Chemotherapy: Post Hoc Analysis of the SCOT Randomized Clinical Trial.
Gögenur, Mikail; Rosen, Andreas Weinberger; Iveson, Timothy; Kerr, Rachel S; Saunders, Mark P; Cassidy, Jim; Tabernero, Josep; Haydon, Andrew; Glimelius, Bengt; Harkin, Andrea; Allan, Karen; Pearson, Sarah; Boyd, Kathleen A; Briggs, Andrew H; Waterston, Ashita; Medley, Louise; Ellis, Richard; Dhadda, Amandeep S; Harrison, Mark; Falk, Stephen; Rees, Charlotte; Olesen, Rene K; Propper, David; Bridgewater, John; Azzabi, Ashraf; Cunningham, David; Hickish, Tamas; Gollins, Simon; Wasan, Harpreet S; Kelly, Caroline; Gögenur, Ismail; Holländer, Niels Henrik.
Affiliation
  • Gögenur M; Center for Surgical Science, Department of Surgery, Zealand University Hospital, Køge, Denmark.
  • Rosen AW; Center for Surgical Science, Department of Surgery, Zealand University Hospital, Køge, Denmark.
  • Iveson T; Southampton University, Southampton, United Kingdom.
  • Kerr RS; Department of Oncology, University of Oxford, Oxford, United Kingdom.
  • Saunders MP; The Christie Hospital, Manchester, United Kingdom.
  • Cassidy J; Glasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.
  • 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.
  • Haydon A; Australasian Gastro-Intestinal Trials Group, Sydney, Australia.
  • Glimelius B; Department of Immunology, Genetics and Pathology, University of Uppsala, Uppsala, Sweden.
  • Harkin A; Glasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.
  • Allan K; Glasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.
  • Pearson S; Oncology Clinical Trials Office, Department of Oncology, University of Oxford, Oxford, United Kingdom.
  • Boyd KA; School of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom.
  • Briggs AH; School of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom.
  • Waterston A; London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Medley L; Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.
  • Ellis R; Royal United Hospital, Bath, United Kingdom.
  • Dhadda AS; Royal Cornwall Hospitals, National Health Service Trust, Cornwall, United Kingdom.
  • Harrison M; Castle Hill Hospital, Hull, United Kingdom.
  • Falk S; Mount Vernon Cancer Centre, Northwood, United Kingdom.
  • Rees C; Bristol Cancer Institute, Bristol, United Kingdom.
  • Olesen RK; Southampton University, Southampton, United Kingdom.
  • Propper D; Department of Oncology, Aalborg University Hospital, Aalborg, Denmark.
  • Bridgewater J; Southampton University, Southampton, United Kingdom.
  • Azzabi A; Barts Cancer Institute, Queen Mary, University of London, London, United Kingdom.
  • Cunningham D; University College London, London, United Kingdom.
  • Hickish T; Newcastle upon Tyne Hospitals, National Health Service Foundation Trust, Newcastle, United Kingdom.
  • Gollins S; Brighton and Sussex University Hospital Trust, Brighton, United Kingdom.
  • Wasan HS; University Hospitals Dorset, Bournemouth University, Bournemouth, United Kingdom.
  • Kelly C; North Wales Cancer Treatment Centre, Rhyl, United Kingdom.
  • Gögenur I; Hammersmith Hospital, Imperial College London, London, United Kingdom.
  • Holländer NH; Glasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.
JAMA Surg ; 2024 Jun 12.
Article in En | MEDLINE | ID: mdl-38865139
ABSTRACT
Importance 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.

Objective:

To analyze the association between the timing of adjuvant chemotherapy after surgery for colorectal cancer and disease-free survival. Design, Setting, and

Participants:

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. Intervention 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. Main Outcomes and

Measures:

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.

Results:

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). Conclusions and Relevance 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. Trial Registration isrctn.org Identifier ISRCTN59757862.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JAMA Surg Year: 2024 Document type: Article Affiliation country: Denmark

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JAMA Surg Year: 2024 Document type: Article Affiliation country: Denmark