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          Resource-Sparing Curative Treatment for Rectal Cancer

          Closed for proposals

          Project Type

          Coordinated Research Project

          Project Code

          E33034

          CRP

          1524

          Approved Date

          11 June 2009

          Status

          Closed

          Start Date

          4 September 2009

          Expected End Date

          4 September 2014

          Completed Date

          26 November 2015

          Description

          The use of a shortened fractionation schedule in the neoadjuvant (preoperative) treatment of rectal cancer has been popular in Europe since its introduction by a Swedish group in 1990.
          This form of treatment is given in one week, thus providing convenience for the patients and resource-sparing for the treatment centres and has been widely tested in a number of European studies in resectable rectal cancer and more recently in unresectable rectal cancer as well, yielding encouraging results. However, this hypofractionated schedule has not been adopted in developing countries yet.
          This CRP attempts to compare the short fractionation to a standard fractionation plus chemotherapy (the control arm) with the double aim of turning unresectable patients resectable (and thus increasing their chances of operability and cure) as well as make the participating centres familiar with this schedule and adopt it in their routine practice.
          Therefore this is a prospective randomized phase III clinical trial comparing a short fractionation schedule of 25 Gy in 5 fractions over one week, to 50 Gy in 25 fractions over 5 weeks combined with chemotherapy as pre-operative treatment for locally advanced, unresectable rectal cancer. The use of pre-operative chemotherapy in the short fractionation arm of the study will be decided during the First Coordination Meeting.

          Objectives

          The primary end point of this study is resectability. This is a short-term outcome which is
          influenced directly by neo-adjuvant treatments. Secondary endpoints include survival, changes
          in CEA, pathological findings at surgery, acute and delayed toxicities, and rates of pelvic control
          of cancer. Although neo-adjuvant treatments may influence many of these secondary
          outcomes, some may be less influenced by neo-adjuvant treatments, and such influence may
          be indirect.

          Specific objectives

          Resectability
          R0 (negative margins) resectability
          Overall survival
          Biological effects of treatment
          Quality of Life
          Economic impact

          Impact

          The CRP potentially has high impact in our MS where radiotherapy resources are inadequate. Use of a short fractionation may allow more patients initially deemed inoperable to receive radical treatment in a timely fashion and proceed to curative surgery.

          Relevance

          Highly relevant in IAEA MS

          CRP Publications

          Type

          Abstract to international meeting

          Year

          2013

          Description

          Oral presentatiion to be given in the annual ALATRO meeting in Cartagena, Colombia, July 2013.

          Country/Organization

          Austria IAEA

          Type

          Abstract to international meeting

          Year

          2013

          Description

          Oral presentatiion to be given in the annual ALATRO meeting in Cartagena, Colombia, July 2013.

          Country/Organization

          Austria IAEA

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