What does NRCT mean in ONCOLOGY
NRCT stands for the National Registry of Childhood Tumours, which is based at Oxford University's Centre for Childhood Cancer Research and Survival (CCRG). It is a national database of medical information related to childhood cancers, including long-term survival rates and outcomes. The NRCT is one of the most comprehensive collections of childhood cancer data in the world and is used to help support research into childhood cancers, as well as helping improve treatment plans for children who are diagnosed with cancer.
NRCT meaning in Oncology in Medical
NRCT mostly used in an acronym Oncology in Category Medical that means National Registry of Childhood Tumours, CCRG at Oxford
Shorthand: NRCT,
Full Form: National Registry of Childhood Tumours, CCRG at Oxford
For more information of "National Registry of Childhood Tumours, CCRG at Oxford", see the section below.
Essential Questions and Answers on National Registry of Childhood Tumours, CCRG at Oxford in "MEDICAL»ONCOLOGY"
What is the National Registry of Childhood Tumours?
The National Registry of Childhood Tumours is a research database run by CCRG at Oxford University which collects and analyses information about childhood cancers. It's purpose is to identify patterns in causes, prognoses and outcomes of cancer in children, as well as to enable better identification and treatment of these diseases.
Why is the National Registry of Childhood Tumours important?
The National Registry of Childhood Tumours helps to advance our understanding of different types of childhood cancer, which can help inform more effective treatments. This research is vital for developing better strategies to diagnose, treat and improve care for cancer affected children.
Who runs the National Registry Of Childhood Tumours?
The CCRG (Childhood Cancer Research Group) at Oxford University run the National registry Of Childhood Tumours. They are committed to creating a comprehensive research database on pediatric tumors that can be used to study future trends in diagnosis and treatment.
How does the National Registry Of Childhood Tumours benefit people with cancer?
By collecting data about childhood cancers from clinical records around the world, researchers can work to identify patterns that may help them understand how certain cancers develop or respond to different treatments so they can be more effectively treated or even prevented in the future. This kind of research will ultimately help improve patient outcomes and increase survival rates for those with cancers.
What kind of data does the National Registry Of Childhood Tumours collect?
The data collected by CCRG includes demographic information, medical histories, diagnosis types, therapies used, clinical follow-ups and other relevant details from each patient record submitted from around the world. This information can then be used by researchers to analyse trends over time and identify any correlations between different factors contributing to improved or worsened patient outcomes.
How many patients have been enrolled in the National Registry Of Childhood Tumours so far?
Since its inception in 2000, over 18500 patients have been enrolled in The National Registry Of Childhood Tumors at present day – a huge success in advancing our knowledge about pediatric cancers worldwide!
What countries have contributed data so far?
To date there have been contributions from countries all around the world - including Australia, India, South Africa, Thailand, Qatar and many others – giving researchers access to an unprecedented wealth of data for studies on pediatric tumor epidemiology and treatment protocols.
How has the work done by the CCRG changed outcomes for children with cancer? A: Thanks to interdisciplinary collaborations across several countries through data collected by The National Registry Of Childhood Tumors at CCRG Oxford University advances have been made that are helping shape practice guidelines and improving patient outcomes overall. Improved early detection methods have allowed more detailed prognostication prior to therapy thus leading to much higher success rates as well as reduced overall costs when it comes treating pediatric cancers.[END] Q: Is there any way I can support The CCRG’s mission?
Thanks to interdisciplinary collaborations across several countries through data collected by The National Registry Of Childhood Tumors at CCRG Oxford University advances have been made that are helping shape practice guidelines and improving patient outcomes overall. Improved early detection methods have allowed more detailed prognostication prior to therapy thus leading to much higher success rates as well as reduced overall costs when it comes treating pediatric cancers.
Final Words:
In conclusion, the National Registry of Childhood Tumours provides important medical data regarding children suffering from cancer which helps clinicians provide more accurate diagnosis, prognosis and treatment plans, enabling more successful outcomes for affected patients. It also serves as an invaluable resource for researchers attempting to uncover new ways of treating this devastating disease through evidence-based research while providing key insight into potential innovative preventative measures designed specifically towards younger individuals suffering from cancerous tumours or conditions.
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