A national pharmacogenetics service

Pharmacogenetics 1

 

An alarming 6.5 per cent of hospital admissions are due to adverse drug reactions. Now a unique drug monitoring service is helping to ensure that drugs prescribed to treat life-threatening diseases don't themselves make patients ill due to serious side effects. The pharmacogenetics service is based in the Purine Research Laboratory, part of GSTS Pathology LLP - the UK's leading supplier of pathology services provided jointly by Guy's and St Thomas' and King's College Hospital NHS Foundation Trusts and Serco plc.

Variation in drug response is often due to specific differences in the genetic make-up between individuals.  By studying genes involved in drug metabolism, the pharmacogenetic researchers can identify markers predicting serious side effects to therapy. Therapy can then be changed in these patients, avoiding hospital stays and treatment failure.

Investment by the Charity in the new service has led to tests for genetic markers to help optimise commonly used drug therapies in cancer and autoimmune conditions. A grant from the Charity of £190,000 has enabled Dr Jeremy Sanderson (Consultant Gastroenterologist) and Dr Marinaki's team in the Purine Research Laboratory to develop a national service to optimise azathioprine therapy for inflammatory bowel disease. With these tests guiding new treatment strategies, azathioprine therapy can now be personalised to unprecedented levels, thereby preventing patients from requiring surgery or more toxic therapies.  Working with Dr Paul Ross in Medical Oncology, the team have identified pharmacogenetic markers predicting serious toxicity to the fluoropyrimidine drugs capecitabine and 5-fluorouracil.  These markers have been brought into the diagnostic service by GSTS Pathology and will directly benefit patients at Guy's and St Thomas' and King's College Hospital and the more than 100,000 patients treated with these drugs each year across the NHS.

In addition to its general funding, the Charity has recognised the positive impact that pharmacogenetics will have on patient care and has awarded £561,000 to fund research to find genetic markers predicting serious side effects to drugs used for the treatment of lung cancer and for preventing rejection in renal transplantation. This research will benefit patients directly. In addition, pharmacogenetic markers have commercial value as diagnostic tests and the use of these diagnostic tests will provide a return on investment for the Charity - for new investment into future health service innovations.

 "Being able to identify the genetic markers which lead to an adverse reaction can make a massive difference to patients, as well as presenting a cost saving to the NHS in avoidable hospitalisation", said Dr Tony Marinaki, Clinical Biochemist.