TOPGEAR: a randomised phase III trial of perioperative ECF chemotherapy versus preoperative chemoradiation plus perioperative ECF chemotherapy for resectable gastric cancer (an international, intergroup trial of the AGITG/TROG/EORTC/NCIC CTG)
Creators
- 1. Peter MacCallum Cancer Centre, Locked Bag 1, A'Beckett Street, Victoria, 8006 (Australia)
- 2. Upper Gastro-intestinal and Soft Tissue Unit, School of Medicine, University of Queensland, Princess Alexandra Hospital, Ipswich Road, Woolloongabba, QLD 4102 (Australia)
- 3. NHMRC Clinical Trials Centre, University of Sydney, Locked bag 77, Camperdown, NSW 1450 (Australia)
- 4. School of Public Health and Preventive Medicine, Monash University, Level 5 The Alfred Centre, 99 Commercial Road, Melbourne, VIC 3004 (Australia)
- 5. Radiation Oncology, University Hospitals Leuven, Department of Oncology, KU, Leuven (Belgium)
- 6. University Cancer Center Leipzig (UCCL), University Medicine Leipzig, Leipzig (Germany)
- 7. European Clinical Research Infrastructure Network, ECRIN-ERIC, Paris Biopark, 5 rue Watt, 75013 Paris (France)
- 8. Mount Sinai Hospital, Rm 1225, 600 University Avenue, Toronto, ON M5G 1X5 (Canada)
- 9. Toronto General Hospital, 9N-955, 200 Elizabeth St, Toronto, ON M5G 2C4 (Canada)
- 10. Princess Margaret Hospital, Rm 5-807, 610 University Avenue, Toronto, M5G 2M9 (Canada)
Description
The optimal management of patients with resectable gastric cancer continues to evolve in Western countries. Following publication of the US Intergroup 0116 and UK Medical Research Council MAGIC trials, there are now two standards of care for adjuvant therapy in resectable gastric cancer, at least in the Western world: postoperative chemoradiotherapy and perioperative epirubicin/cisplatin/fluorouracil (ECF) chemotherapy. We hypothesize that adding chemoradiation to standard perioperative ECF chemotherapy will achieve further survival gains. We also believe there are advantages to administering chemoradiation in the preoperative rather than postoperative setting. In this article, we describe the TOPGEAR trial, which is a randomised phase III trial comparing control arm therapy of perioperative ECF chemotherapy with experimental arm therapy of preoperative chemoradiation plus perioperative ECF chemotherapy. Eligible patients with resectable adenocarcinoma of the stomach or gastroesophageal junction will be randomized to receive either perioperative chemotherapy alone (3 preoperative and 3 postoperative cycles of ECF) or perioperative chemotherapy plus preoperative chemoradiation. In the chemoradiation arm, patients receive 2 cycles of ECF plus chemoradiation prior to surgery, and then following surgery 3 further cycles of ECF are given. The trial is being conducted in two Parts; Part 1 (phase II component) has recruited 120 patients with the aim of assessing feasibility, safety and preliminary efficacy of preoperative chemoradiation. Part 2 (phase III component) will recruit a further 632 patients to provide a total sample size of 752 patients. The primary endpoint of the phase III trial is overall survival. The trial includes quality of life and biological substudies, as well as a health economic evaluation. In addition, the trial incorporates a rigorous quality assurance program that includes real time central review of radiotherapy plans and central review of surgical technique. TOPGEAR is an international, intergroup collaboration led by the Australasian Gastro-Intestinal Trials Group (AGITG), in collaboration with the Trans-Tasman Radiation Oncology Group (TROG), European Organisation for Research and Treatment of Cancer (EORTC) and the NCIC Clinical Trials Group. It addresses a globally significant question that will help inform future international standards for clinical practice in resectable gastric cancer
Availability note (English)
Available from http://dx.doi.org/10.1186/s12885-015-1529-x; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507314Additional details
Identifiers
Publishing Information
- Journal Title
- BMC cancer (Online)
- Journal Volume
- 15
- Journal Page Range
- vp.
- ISSN
- 1471-2407
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47084146
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CARCINOMAS; CHEMOTHERAPY; CLINICAL TRIALS; COMBINED THERAPY; PATIENTS; QUALITY ASSURANCE; RADIOTHERAPY; STANDARD OF LIVING; SURGERY
- Descriptors DEC
- DISEASES; MEDICINE; NEOPLASMS; NUCLEAR MEDICINE; RADIOLOGY; TESTING; THERAPY
Optional Information
- Copyright
- Copyright (c) Leong et al. 2015
- Notes
- PMCID: PMC4507314; PMID: 26194186; PUBLISHER-ID: 1529; OAI: oai:pubmedcentral.nih.gov:4507314