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Laparoscopically assisted versus open oesophagectomy for patients with oesophageal cancer—the Randomised Oesophagectomy: Minimally Invasive or Open (ROMIO) study: protocol for a randomised controlled trial (RCT)
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IntroductionSurgery (oesophagectomy), with neoadjuvant chemo(radio)therapy, is the main curative treatment for patients with oesophageal cancer. Several surgical approaches can be used to remove an oesophageal tumour. The Ivor Lewis (two-phase procedure) is usually used in the UK. This can be performed as an open oesophagectomy (OO), a laparoscopically assisted oesophagectomy (LAO) or a totally minimally invasive oesophagectomy (TMIO). All three are performed in the National Health Service, with LAO and OO the most common. However, there is limited evidence about which surgical approach is best for patients in terms of survival and postoperative health-related quality of life.Methods and analysisWe will undertake a UK multicentre randomised controlled trial to compare LAO with OO in adult patients with oesophageal cancer. The primary outcome is patient-reported physical function at 3 and 6 weeks postoperatively and 3 months after randomisation. Secondary outcomes include: postoperative complications, survival, disease recurrence, other measures of quality of life, spirometry, success of patient blinding and quality assurance measures. A cost-effectiveness analysis will be performed comparing LAO with OO. We will embed a randomised substudy to evaluate the safety and evolution of the TMIO procedure and a qualitative recruitment intervention to optimise patient recruitment. We will analyse the primary outcome using a multi-level regression model. Patients will be monitored for up to 3 years after their surgery.Ethics and disseminationThis study received ethical approval from the South-West Franchay Research Ethics Committee. We will submit the results for publication in a peer-reviewed journal.Trial registration numberNCT10386621.
BMJ
Rachel C Brierley
Daisy Gaunt
Chris Metcalfe
Jane M Blazeby
Natalie S Blencowe
Marcus Jepson
Richard G Berrisford
Kerry N L Avery
William Hollingworth
Caoimhe T Rice
Aida Moure-Fernandez
Newton Wong
Joanna Nicklin
Anni Skilton
Alex Boddy
James P Byrne
Tim Underwood
Ravi Vohra
James A Catton
Kish Pursnani
Rachel Melhado
Bilal Alkhaffaf
Richard Krysztopik
Peter Lamb
Lucy Culliford
Chris Rogers
Benjamin Howes
Katy Chalmers
Sian Cousins
Jackie Elliott
Jenny Donovan
Rachael Heys
Robin A Wickens
Paul Wilkerson
Andrew Hollowood
Christopher Streets
Dan Titcomb
Martyn Lee Humphreys
Tim Wheatley
Grant Sanders
Arun Ariyarathenam
Jamie Kelly
Fergus Noble
Graeme Couper
Richard J E Skipworth
Chris Deans
Sukhbir Ubhi
Robert Williams
David Bowrey
David Exon
Paul Turner
Vinutha Daya Shetty
Ram Chaparala
Khurshid Akhtar
Naheed Farooq
Simon L Parsons
Neil T Welch
Rebecca J Houlihan
Joanne Smith
Rachel Schranz
Nicola Rea
Jill Cooke
Alexandra Williams
Carolyn Hindmarsh
Sally Maitland
Lucy Howie
Christopher Paul Barham
Title: Laparoscopically assisted versus open oesophagectomy for patients with oesophageal cancer—the Randomised Oesophagectomy: Minimally Invasive or Open (ROMIO) study: protocol for a randomised controlled trial (RCT)
Description:
IntroductionSurgery (oesophagectomy), with neoadjuvant chemo(radio)therapy, is the main curative treatment for patients with oesophageal cancer.
Several surgical approaches can be used to remove an oesophageal tumour.
The Ivor Lewis (two-phase procedure) is usually used in the UK.
This can be performed as an open oesophagectomy (OO), a laparoscopically assisted oesophagectomy (LAO) or a totally minimally invasive oesophagectomy (TMIO).
All three are performed in the National Health Service, with LAO and OO the most common.
However, there is limited evidence about which surgical approach is best for patients in terms of survival and postoperative health-related quality of life.
Methods and analysisWe will undertake a UK multicentre randomised controlled trial to compare LAO with OO in adult patients with oesophageal cancer.
The primary outcome is patient-reported physical function at 3 and 6 weeks postoperatively and 3 months after randomisation.
Secondary outcomes include: postoperative complications, survival, disease recurrence, other measures of quality of life, spirometry, success of patient blinding and quality assurance measures.
A cost-effectiveness analysis will be performed comparing LAO with OO.
We will embed a randomised substudy to evaluate the safety and evolution of the TMIO procedure and a qualitative recruitment intervention to optimise patient recruitment.
We will analyse the primary outcome using a multi-level regression model.
Patients will be monitored for up to 3 years after their surgery.
Ethics and disseminationThis study received ethical approval from the South-West Franchay Research Ethics Committee.
We will submit the results for publication in a peer-reviewed journal.
Trial registration numberNCT10386621.
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