“… A pattern of genetic defects in tumours could indicate whether ovarian cancer patients will respond to common chemotherapy drugs before treatment starts, reveals a Cancer Research UK study published in the Proceedings of the National Academy of Sciences … The researchers studied patterns of gene expression that indicate high levels of abnormal chromosomes or chromosomal instability (CIN) in cancer. …Patients with high levels of the CIN gene pattern were more resistant to paclitaxel. Crucially, patients with high levels of CIN responded well to carboplatin – another commonly used ovarian cancer drug. In contrast, tumours with low levels of CIN were resistant to carboplatin but responded to paclitaxel. …”
“Cancer Research UK scientists discover pattern of genetic faults to predict cancer drug success
Cancer Research UK
MONDAY 4 MAY 2009
Cancer Research UK Press Release
A pattern of genetic defects in tumours could indicate whether ovarian cancer patients will respond to common chemotherapy drugs before treatment starts, reveals a Cancer Research UK study published in the Proceedings of the National Academy of Sciences* today (Monday).
They then investigated whether CIN can help doctors identify which patients are most likely to respond to the chemotherapy drugs paclitaxel or carboplatin in a prospective clinical trial of ovarian cancer patients. Patients with high levels of the CIN gene pattern were more resistant to paclitaxel. Crucially, patients with high levels of CIN responded well to carboplatin – another commonly used ovarian cancer drug. In contrast, tumours with low levels of CIN were resistant to carboplatin but responded to paclitaxel.
The researchers believe clinical tests for CIN – which can be identified by dye-stained cells under a microscope – may be available within five years, saving patients from ineffective chemotherapy and leading to personalised treatment.
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Senior author Dr. Julian Downward, based at Cancer Research UK’s London Research Institute, said: ‘Our work suggests that resistance to paclitaxel is driven by distinct irregularities in the cancer cell that lead to abnormal cancer cell division. These changes may also render cancers more sensitive to carboplatin treatment.’
Each year in the UK over 6,600 cases of ovarian cancer are diagnosed, and around 4,500 women die from the disease.
Senior co-author Dr James Brenton, based at Cancer Research UK’s Cambridge Research Institute and an ovarian cancer clinician at Addenbrooke’s Hospital said: ‘All ovarian cancer patients are treated with carboplatin but most who have more aggressive cancers are treated with paclitaxel as well. As we don’t know which patients will benefit from having additional paclitaxel it is very important that we develop better tests to choose the right drugs for individual patients.’
Lead author Dr Charles Swanton, based at Cancer Research UK’s London Research Institute and at the Royal Marsden Hospital said: ‘Until now it has been difficult to predict which patients may benefit from individual chemotherapy drugs before treatment. We hope that simple tests based on these findings will save patients from unnecessary treatments with paclitaxel that can have severe side-effects with limited benefit.’
Dr Lesley Walker, director of cancer information at Cancer Research UK, said: ‘This is an excellent example of how basic science can translate into discoveries that improve treatments given to patients. One of Cancer Research UK’s goals is to create more targeted treatments with fewer side effects, and this is a crucially important step in achieving this – potentially personalising the treatment of thousands of people with cancer.’
For media enquiries please contact the Cancer Research UK press office on 020 7061 8300 or, out-of-hours, the duty press officer on 07050 264 059.
Notes to editors:
Normal human cells each have 23 pairs of chromosomes, which hold all of our genes. A key part of mitosis is making sure each of the two resulting daughter cells has the right number of correct chromosomes. A complex set of proteins controls this process – the so-called ‘spindle assembly checkpoint‘. If these proteins don’t work properly, cells can end up with too many or too few chromosomes, a condition known as chromosomal instability.
* Chromosomal Instability Determines Taxane Response. Swanton et al. 2009. Proceedings of the National Academy of Sciences.
** The drug Herceptin has been shown to provide clinical benefit to patients with high levels of HER2 receptor on the surface of, although how to accurately determine HER2 status is still under discussion. Around a quarter of breast cancers has HER2 on the surface of cells and tests for this are done before treatment.
*** This method for assessing CIN in colon cancer is currently being studied in an early clinical trial at the Royal Marsden Hospital. The clinical trial, called CINATRA, is testing whether doctors can predict whether a paclitaxel-like drug is effective at treating colorectal tumours that do not have CIN.
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The pattern for detecting CIN was first discovered in 2006 by study co-author Dr Zoltan Szallasi.”
About Cancer Research UK
Cancer Research UK (CRUK) launched in February 2002 following the merger of The Cancer Research Campaign and Imperial Cancer Research Fund. CRUK is the world’s leading independent organization dedicated to cancer research. The charity supports research into all aspects of cancer through the work of more than 4,500 scientists, doctors and nurses. CRUK is the European leader in the development of novel anti-cancer treatments.
Source: Cancer Research UK scientists discover pattern of genetic faults to predict cancer drug success, Cancer Research UK Press Release, Cancer Research UK, May 4, 2009.