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Open Access Highly Accessed Study protocol

A randomised trial of robotic and open prostatectomy in men with localised prostate cancer

Robert A Gardiner123*, John Yaxley2, Geoff Coughlin2, Nigel Dunglison2, Stefano Occhipinti4, Sandra Younie5, Rob Carter5, Scott Williams6, Robyn J Medcraft12, Nigel Bennett1, Martin F Lavin17 and Suzanne Kathleen Chambers1348

Author Affiliations

1 University of Queensland Centre for Clinical Research, Royal Brisbane Hospital, Queensland, Australia

2 Department of Urology, Royal Brisbane Hospital, Queensland, Australia

3 Edith Cowan University Health and Wellness Institute, Edith Cowan University, Western Australia, Australia

4 Griffith Health Institute, Griffith University, Queensland Victoria,, Australia

5 Deakin Health Economics, Deakin University, Victoria, Australia

6 Peter MacCallum Cancer Centre, Queensland, Australia

7 Radiation Biology and Oncology Laboratory, Queensland Institute of Medical Research, Victoria, Australia

8 Cancer Council Queensland, Queensland, Australia

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BMC Cancer 2012, 12:189  doi:10.1186/1471-2407-12-189

Published: 25 May 2012

Abstract

Background

Prostate cancer is the most common male cancer in the Western world however there is ongoing debate about the optimal treatment strategy for localised disease. While surgery remains the most commonly received treatment for localised disease in Australia more recently a robotic approach has emerged as an alternative to open and laparoscopic surgery. However, high level data is not yet available to support this as a superior approach or to guide treatment decision making between the alternatives. This paper presents the design of a randomised trial of Robotic and Open Prostatectomy for men newly diagnosed with localised prostate cancer that seeks to answer this question.

Methods/design

200 men per treatment arm (400 men in total) are being recruited after diagnosis and before treatment through a major public hospital outpatient clinic and randomised to 1) Robotic Prostatectomy or 2) Open Prostatectomy. All robotic prostatectomies are being performed by one surgeon and all open prostatectomies are being performed by one other surgeon. Outcomes are being measured pre-operatively and at 6 weeks and 3, 6, 12 and 24 months post-surgery. Oncological outcomes are being related to positive surgical margins, biochemical recurrence +/− the need for further treatment. Non-oncological outcome measures include: pain, physical and mental functioning, fatigue, summary (preference-based utility scores) and domain-specific QoL (urinary incontinence, bowel function and erectile function), cancer specific distress, psychological distress, decision-related distress and time to return to usual activities. Cost modelling of each approach, as well as full economic appraisal, is also being undertaken.

Discussion

The study will provide recommendations about the relative benefits of Robotic and Open Prostatectomy to support informed patient decision making about treatment for localised prostate cancer; and to assist in treatment services planning for this patient group.

Trial registration

ACTRN12611000661976