Evidence map›Paper›PMID 41512219›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2026

Three Versus 6 Months of Adjuvant Oxaliplatin-Fluoropyrimidine Chemotherapy for Colorectal Cancer: Final Results of SCOT-An International, Randomized, Phase III, Noninferiority Trial.

Timothy Iveson, Mark P Saunders, Caroline Kelly, Rachel S Kerr, Jim Cassidy, Niels Henrik Hollander, Josep Tabernero, Andrew Haydon, Bengt Glimelius, Andrea Harkin and 22 more

Abstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

32 authors.

Timothy IvesonUniversity of Southampton, Southampton, United Kingdom.ORCID 0000-0002-4681-2712
Mark P SaundersThe Christie Hospital, Manchester, United Kingdom.
Caroline KellyGlasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-5330-7888
Rachel S KerrDepartment of Oncology, University of Oxford, Oxford, United Kingdom.
Jim CassidyGlasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.
Niels Henrik HollanderDepartment of Oncology and Palliative Care, Zealand University Hospital, Naestved, Denmark.ORCID 0000-0003-2509-2231
Josep TaberneroVall d'Hebron Hospital Campus and Institute of Oncology (VHIO), UVic-UCC, IOB-Quiron, CIBERONC, Barcelona, Spain.ORCID 0000-0002-2495-8139
Andrew HaydonAustralasian Gastro-Intestinal Trials Group (AGITG), Alfred Hospital, Melbourne, Australia.ORCID 0000-0002-4631-5855
Bengt GlimeliusDepartment of Immunology, Genetics and Pathology, University of Uppsala, Uppsala, Sweden.ORCID 0000-0002-5440-791X
Andrea HarkinGlasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-8831-7381
Karen AllanGlasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.
John McQueenGlasgow Oncology Clinical Trials Unit, School of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0001-5950-8819
Sarah PearsonOCTO, Department of Oncology, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-5386-1953
Kathleen A BoydInstitute of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-9764-0113
Andrew H BriggsInstitute of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom.
Ashita WaterstonBeatson West of Scotland Cancer Centre, NHS GGC HB, Glasgow, United Kingdom.
Louise MedleyRoyal United Hospital, Bath, United Kingdom.ORCID 0000-0003-0725-3812
Richard EllisRoyal Cornwall Hospitals NHS Trust, Cornwall, United Kingdom.
Amandeep S DhaddaCastle Hill Hospital, Hull, United Kingdom.
Mark HarrisonMount Vernon Cancer Centre, Northwood, United Kingdom.
Stephen FalkBristol Cancer Institute, Bristol, United Kingdom.
Charlotte ReesSouthampton University Hospital NHS Foundation Trust, Southampton, United Kingdom.
Rene K OlesenDepartment of Oncology, Aarhus University Hospital, Aarhus C, Denmark.ORCID 0000-0002-3331-6904
David PropperBarts Cancer Institute, Queen Mary, University of London, London, United Kingdom.ORCID 0000-0002-4274-5460
John BridgewaterUniversity College London, London, United Kingdom (part funded by the UCLH/UCL Biomedical Research Centre).ORCID 0000-0001-9186-1604
Ashraf AzzabiNewcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle, United Kingdom.ORCID 0009-0005-5278-1835
David CunninghamRoyal Marsden, London, United Kingdom (funded by NIHR BRC at the Royal Marsden).ORCID 0000-0001-5158-1069
Tamas HickishUniversity Hospitals Dorset/Bournemouth University, Bournemouth, United Kingdom.ORCID 0000-0001-6770-7279
Simon GollinsNorth Wales Cancer Treatment Centre, Rhyl, United Kingdom.
Harpreet S WasanHammersmith Hospital, Imperial College London, London, United Kingdom.ORCID 0000-0002-6268-2030
David ChurchDepartment of Oncology, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-4617-962X
Enric DomingoDepartment of Oncology, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-4390-8767

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adjuvant chemotherapy for colorectal cancer (CRC) with oxaliplatin and fluoropyrimidine was traditionally given for 6 months but is associated with cumulative peripheral neuropathy. The SCOT study (ISRCTN59757862) was an international, randomized, phase III, noninferiority trial investigating treatment reduction from 6 to 3 months. It originally reported noninferior disease-free survival with reduced toxicity and improved quality of life for 3 months of treatment in 6,088 patients. Here, we report overall survival (OS) with 38 months of additional follow-up. Patients with high-risk stage II and stage III CRC were assigned (1:1) to receive 3 or 6 months of either capecitabine and oxaliplatin (CAPOX) or infusional fluorouracil, leucovorin, and oxaliplatin (FOLFOX; bolus and infused fluorouracil with oxaliplatin) that were selected before random assignment. With a median of 113 months follow-up and 1,255 OS events, 5-year OS for 3 versus 6 months of treatment was 82.4% in both groups (hazard ratio, 0.96; 95% CI, 0.8 to 1.07), proving noninferiority of 3 months of treatment. Noninferiority of 3 months of treatment for OS was also shown in 1,087 patients with rectal cancer. The duration effect is regimen-dependent with noninferiority shown for CAPOX but not for FOLFOX. In summary, SCOT has shown noninferiority for OS with 3 months of adjuvant chemotherapy treatment, which should be recommended for most patients.

Identifiers

PMID41512219
PMCPMC12931879

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.