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   Infocentre

Last Update: 07-07-2014  
Related category(ies):
Health & life sciences  |  Special Collections

 

Countries involved in the project described in the article:
France  |  Germany  |  Italy  |  Spain  |  United Kingdom
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Why cancer drugs affect young children differently

Cancer drugs save lives, but they are highly toxic. Using the right amounts is crucial. EU-funded research focusing on doxorubicin, one of the main drugs used in chemotherapy, has generated new knowledge that will help to refine the dosages for children.

Photo of baby with a headscarf beating the disease

© Gelpi - Fotolia.com

Getting the balance right in chemotherapy is a conundrum. Give too much of these powerful drugs, and the problems they cause may outweigh the potential benefits. Give too little and the benefit could be reduced. Much depends on the speed at which the body eliminates – or ‘clears’ – the drug. This clearance rate can vary greatly from one person to another.

The findings of the EPOC project indicate that clearance rates for doxorubicin, corrected for body size, are similar in older children and in adults, but that children under three eliminate the drug more slowly.

This observation, which suggests that the drug concentrations achieved in very young children may be higher than in those in older patients, has implications for cancer treatment and could help to develop strategies to reduce the risk of serious side effects.

A delicate balance

In addition to side effects during the treatment, there can also be long-term implications: some drugs can cause problems that persist or occur after the therapy has ended. Above a defined cumulative dose, doxorubicin, for example, can permanently weaken the heart. This risk must be taken into account in order to secure the best chances of patients being cured of their cancer and going on to lead long, healthy lives.

“There are two considerations here,” says project coordinator Professor Alan Boddy of Newcastle University. “One is that you wouldn’t want to not give the drug, and that you would want to give the appropriate dose of the drug to maximise the chance of it working. Another is that a lot of the patients treated with this drug have a prospect of very long-term survival, and you want to avoid chronic side effects that may result from the treatment.”

Better knowledge, better treatment

Dosages for children are often derived from those used for adults, adjusted for body size, and may also be specific to the type of tumour. While the success rates of these treatments are very high, this approach does not necessarily account for the fact that children aren’t simply small adults. New insights could, therefore, help to make the treatment of childhood cancers more effective and safe.

The need for research in this area had been highlighted by the European Medicines Agency (EMA) in its Priority List for Studies into Paediatric Medicinal Products. EPOC set out to provide the required information for doxorubicin.

To do so, the researchers collected data from 100 chemotherapy patients aged from 0 to 17. As childhood cancers are, luckily, quite rare, finding enough patients for the study led to the participation of a number of clinical centres in different EU countries.

The research, which was non-interventional and did not expose the children to any additional risk, involved 20 clinical centres in 4 countries. It was divided into three age groups: the under-threes, children aged 3 to 11, and patients aged 12 to 17.

The difference in clearance was one of the team’s main observations. “It suggests that we need to know more about what influences the elimination of this drug in those very young children,” Prof. Boddy notes. “To some extent, the study has generated new questions as well.”

The team is also looking into the possibilities of using its data to personalise treatment of children with cancer, for example through an assessment of how genetic differences among patients may influence the risk of damage to the heart.

EPOC ended in October 2013, and the team is disseminating the results. Professor Boddy and his colleagues have approached the EMA about incorporating the information into the summary of product characteristics for doxorubicin. They are also collaborating with the teams involved in the EU-funded PANCARE network, which focuses on the long-term implications of paediatric cancer treatment.

 

Project details

  • Project acronym: EPOC
  • Participants: UK (Coordinator), Italy, France, Spain, Germany
  • Project FP7 222910
  • Total costs: € 2 575 594
  • EU contribution: € 1 997 862
  • Duration: February 2009 - October 2013

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