xml version="1.0" encoding="iso-8859-1"?> The Institute of Cancer Research: Epidemiology Section : Clinical Trials and Statistics Unit
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Research
Research Groups: Section of Clinical Trials

Director: Judith Bliss
Deputy Director: Emma Hall

The Clinical Trials and Statistics Unit became an independent research section in January 2004

History

The Clinical Trials and Statistics Unit was established in the 1980s at The Institute Of Cancer Research (ICR) as part of the Section of Epidemiology. Under Judith Bliss’s leadership the ICR-CTSU has developed from a small local statistical support group into an independent research section with a national reputation and an increasing international perspective. The ICR-CTSU receives core funding from Cancer Research UK.  

The main objective of the ICR-CTSU is to design, initiate, conduct and analyse national and international randomised clinical trials of cancer treatment which will directly influence routine clinical practice within the National Health Service and worldwide.

Our trials form an important component of the National Cancer Research Networks portfolio of randomised trials in breast cancer, melanoma and urological cancers.                                   

The ICR-CTSU also provides a randomisation service for 24 Phase II and III trials run locally (Royal Marsden Hospital Trust and other Trusts in the South-West London Cancer Research Network).

During 2003 we have:

  • become an NCRI accredited trials unit
  • begun exploitation of data from large trials such as START  and TACT which is helping to answer subsidiary questions about disease and its effect on patients' quality of life
  • completed accrual of over 4,000 patients, in under 30 months, to the UK TACT trial assessing sequential Taxotere as adjuvant chemotherapy in early breast cancer
  • developed three new trials: MARS, PARSPORT and SOFEA

Associated research

Integral Quality of Life (QOL) studies are routinely conducted as part of ICR-CTSU’s clinical trials.   For three of our breast cancer trials (ABC, START, and TACT) similar instruments have been used, thus providing datasets that can be combined to provide highly detailed QOL data on large numbers of breast cancer patients (eg single measures such as separate anxiety and depression levels can be compared and contrasted between populations participating in different trials).  

The added value of collecting histological specimens (bloods, tumours) within large scale randomised trials is well recognised by ICR-CTSU and translational research forms a key component of our collaborative research programme.  

Summary of Current Trials

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Highlight of 2003

Associated Research

Summary of Current Trials

Summary poster

Last Updated:
January 28, 2005

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