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3-month versus 6-month adjuvant chemotherapy for patients with high-risk stage II and III colorectal cancer: 3-year follow-up of the SCOT non-inferiority RCT.
Iveson, Timothy; Boyd, Kathleen A; Kerr, Rachel S; Robles-Zurita, Jose; Saunders, Mark P; Briggs, Andrew H; Cassidy, Jim; Hollander, Niels Henrik; Tabernero, Josep; Haydon, Andrew; Glimelius, Bengt; Harkin, Andrea; Allan, Karen; McQueen, John; Pearson, Sarah; Waterston, Ashita; Medley, Louise; Wilson, Charles; Ellis, Richard; Essapen, Sharadah; Dhadda, Amandeep S; Harrison, Mark; Falk, Stephen; Raouf, Sherif; Rees, Charlotte; Olesen, Rene K; Propper, David; Bridgewater, John; Azzabi, Ashraf; Farrugia, David; Webb, Andrew; Cunningham, David; Hickish, Tamas; Weaver, Andrew; Gollins, Simon; Wasan, Harpreet; Paul, James.
Afiliación
  • Iveson T; Southampton University Hospital NHS Foundation Trust, Southampton, UK.
  • Boyd KA; Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
  • Kerr RS; Department of Oncology, University of Oxford, Oxford, UK.
  • Robles-Zurita J; Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
  • Saunders MP; The Christie Hospital NHS Foundation Trust, Manchester, UK.
  • Briggs AH; Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
  • Cassidy J; Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
  • Hollander NH; Department of Oncology and Palliative Care, Zealand University Hospital, Naestved, Denmark.
  • Tabernero J; Vall d'Hebron University Hospital and Institute of Oncology, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Haydon A; Australasian Gastro-Intestinal Trials Group, Camperdown, NSW, Australia.
  • Glimelius B; University of Uppsala, Uppsala, Sweden.
  • Harkin A; Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
  • Allan K; Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
  • McQueen J; Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
  • Pearson S; Oncology Clinical Trials Office, Department of Oncology, University of Oxford, Oxford, UK.
  • Waterston A; Beatson West of Scotland Cancer Centre, Glasgow, UK.
  • Medley L; Royal United Hospital, Bath, UK.
  • Wilson C; Addenbrooke's Hospital, Cambridge, UK.
  • Ellis R; Royal Cornwall Hospitals NHS Trust, Cornwall, UK.
  • Essapen S; St Luke's Cancer Centre, Royal Surrey County Hospital NHS Foundation Trust, Guildford, UK.
  • Dhadda AS; Castle Hill Hospital, Hull, UK.
  • Harrison M; Mount Vernon Cancer Centre, Northwood, UK.
  • Falk S; Bristol Cancer Institute, Bristol, UK.
  • Raouf S; Barking Havering and Redbridge University Hospital NHS Trust, Barking, UK.
  • Rees C; Southampton University Hospital NHS Foundation Trust, Southampton, UK.
  • Olesen RK; Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
  • Propper D; Barts Cancer Institute, Queen Mary University of London, London, UK.
  • Bridgewater J; Department of Oncology, University College London, London, UK.
  • Azzabi A; Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Farrugia D; Gloucestershire Oncology Centre, Cheltenham General Hospital, UK.
  • Webb A; Brighton and Sussex University Hospital Trust, Brighton, UK.
  • Cunningham D; Royal Marsden NHS Foundation Trust, London, UK.
  • Hickish T; Poole Hospital NHS Foundation Trust, Poole, UK.
  • Weaver A; Department of Oncology, Oxford University Hospitals Foundation Trust, Oxford, UK.
  • Gollins S; North Wales Cancer Treatment Centre, Rhyl, UK.
  • Wasan H; Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.
  • Paul J; The Christie Hospital NHS Foundation Trust, Manchester, UK.
Health Technol Assess ; 23(64): 1-88, 2019 12.
Article en En | MEDLINE | ID: mdl-31852579
ABSTRACT

BACKGROUND:

Oxaliplatin and fluoropyrimidine chemotherapy administered over 6 months is the standard adjuvant regimen for patients with high-risk stage II or III colorectal cancer. However, the regimen is associated with cumulative toxicity, characterised by chronic and often irreversible neuropathy.

OBJECTIVES:

To assess the efficacy of 3-month versus 6-month adjuvant chemotherapy for colorectal cancer and to compare the toxicity, health-related quality of life and cost-effectiveness of the durations.

DESIGN:

An international, randomised, open-label, non-inferiority, Phase III, parallel-group trial.

SETTING:

A total of 244 oncology clinics from six countries UK (England, Scotland, Wales and Northern Ireland), Denmark, Spain, Sweden, Australia and New Zealand.

PARTICIPANTS:

Adults aged ≥ 18 years who had undergone curative resection for high-risk stage II or III adenocarcinoma of the colon or rectum.

INTERVENTIONS:

The adjuvant treatment regimen was either oxaliplatin and 5-fluorouracil or oxaliplatin and capecitabine, randomised to be administered over 3 or 6 months. MAIN OUTCOME

MEASURES:

The primary outcome was disease-free survival. Overall survival, adverse events, neuropathy and health-related quality of life were also assessed. The main cost categories were chemotherapy treatment and hospitalisation. Cost-effectiveness was assessed through incremental cost comparisons and quality-adjusted life-year gains between the options and was reported as net monetary benefit using a willingness-to-pay threshold of £30,000 per quality-adjusted life-year per patient.

RESULTS:

Recruitment is closed. In total, 6088 patients were randomised (3044 per group) between 27 March 2008 and 29 November 2013, with 6065 included in the intention-to-treat analyses (3-month analysis, n = 3035; 6-month analysis, n = 3030). Follow-up for the primary analysis is complete. The 3-year disease-free survival rate in the 3-month treatment group was 76.7% (standard error 0.8%) and in the 6-month treatment group was 77.1% (standard error 0.8%), equating to a hazard ratio of 1.006 (95% confidence interval 0.909 to 1.114; p-value for non-inferiority = 0.012), confirming non-inferiority for 3-month adjuvant chemotherapy. Frequent adverse events (alopecia, anaemia, anorexia, diarrhoea, fatigue, hand-foot syndrome, mucositis, sensory neuropathy, neutropenia, pain, rash, altered taste, thrombocytopenia and watery eye) showed a significant increase in grade with 6-month duration; the greatest difference was for sensory neuropathy (grade ≥ 3 was 4% for 3-month vs.16% for 6-month duration), for which a higher rate of neuropathy was seen for the 6-month treatment group from month 4 to ≥ 5 years (p < 0.001). Quality-of-life scores were better in the 3-month treatment group over months 4-6. A cost-effectiveness analysis showed 3-month treatment to cost £4881 less over the 8-year analysis period, with an incremental net monetary benefit of £7246 per patient.

CONCLUSIONS:

The study achieved its primary end point, showing that 3-month oxaliplatin-containing adjuvant chemotherapy is non-inferior to 6 months of the same regimen; 3-month treatment showed a better safety profile and cost less. For future work, further follow-up will refine long-term estimates of the duration effect on disease-free survival and overall survival. The health economic analysis will be updated to include long-term extrapolation for subgroups. We expect these analyses to be available in 2019-20. The Short Course Oncology Therapy (SCOT) study translational samples may allow the identification of patients who would benefit from longer treatment based on the molecular characteristics of their disease. TRIAL REGISTRATION Current Controlled Trials ISRCTN59757862 and EudraCT 2007-003957-10.

FUNDING:

This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 23, No. 64. See the NIHR Journals Library website for further project information. This research was supported by the Medical Research Council (transferred to NIHR Evaluation, Trials and Studies Coordinating Centre - Efficacy and Mechanism Evaluation; grant reference G0601705), the Swedish Cancer Society and Cancer Research UK Core Clinical Trials Unit Funding (funding reference C6716/A9894).
Patients diagnosed with bowel cancer are likely to have surgery to remove the tumour. Patients diagnosed with a more advanced stage of the disease are then likely to be offered what is known as adjuvant chemotherapy ­ chemotherapy to kill any cancer cells that have already spread but cannot be seen. Adjuvant chemotherapy is usually given over 6 months using two medicines known as oxaliplatin and fluoropyrimidine. This chemotherapy has side effects of diarrhoea, nausea and vomiting, and it reduces the numbers of cells in the blood. It can also damage nerves, which causes discomfort, numbness and tingling; in some cases, this can go on for years. These side effects are more likely to develop with longer treatment. This study looked at whether or not shortening the time over which patients were given oxaliplatin and fluoropyrimidine chemotherapy reduced its effectiveness. In this large study of over 6000 patients, half of the patients were allocated by chance to be treated for 3 months and the other half to be treated for 6 months. Reducing the time that patients had chemotherapy from 6 months to 3 months did not make the treatment less effective. When patients treated with chemotherapy over 3 months were compared with those treated over 6 months, 77% of patients in both groups were well with no detectable disease 3 years after surgery. Patients were less likely to get side effects with 3-month chemotherapy. In particular, the chance of persistent long-term nerve damage was lower, resulting in patients with 3-month chemotherapy having better health-related quality of life. Overall, the study showed that 3-month adjuvant chemotherapy for patients with bowel cancer is as effective as 6-month adjuvant chemotherapy and causes fewer side effects.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 3_ND Problema de salud: 3_diarrhea Asunto principal: Neoplasias Colorrectales / Protocolos de Quimioterapia Combinada Antineoplásica / Supervivencia sin Enfermedad / Capecitabina / Fluorouracilo / Oxaliplatino Tipo de estudio: Clinical_trials / Etiology_studies / Health_technology_assessment / Observational_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa / Oceania Idioma: En Revista: Health Technol Assess Asunto de la revista: PESQUISA EM SERVICOS DE SAUDE / TECNOLOGIA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 3_ND Problema de salud: 3_diarrhea Asunto principal: Neoplasias Colorrectales / Protocolos de Quimioterapia Combinada Antineoplásica / Supervivencia sin Enfermedad / Capecitabina / Fluorouracilo / Oxaliplatino Tipo de estudio: Clinical_trials / Etiology_studies / Health_technology_assessment / Observational_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa / Oceania Idioma: En Revista: Health Technol Assess Asunto de la revista: PESQUISA EM SERVICOS DE SAUDE / TECNOLOGIA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido
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