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Development of a best-practice clinical guideline for the use of bleomycin in the treatment of germ cell tumours in the UK

Bleomycin, a cytotoxic chemotherapy agent, forms a key component of curative regimens for lymphoma and germ cell tumours. It can be associated with severe toxicity, long-term complications and even death in extreme cases. There is a lack of evidence or consensus on how to prevent and monitor bleomyc...

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Autores principales: Watson, Robert A., De La Peña, Hugo, Tsakok, Maria T., Joseph, Johnson, Stoneham, Sara, Shamash, Jonathan, Joffe, Johnathan, Mazhar, Danish, Traill, Zoe, Ho, Ling-Pei, Brand, Sue, Protheroe, Andrew S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219480/
https://www.ncbi.nlm.nih.gov/pubmed/30356125
http://dx.doi.org/10.1038/s41416-018-0300-x
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author Watson, Robert A.
De La Peña, Hugo
Tsakok, Maria T.
Joseph, Johnson
Stoneham, Sara
Shamash, Jonathan
Joffe, Johnathan
Mazhar, Danish
Traill, Zoe
Ho, Ling-Pei
Brand, Sue
Protheroe, Andrew S.
author_facet Watson, Robert A.
De La Peña, Hugo
Tsakok, Maria T.
Joseph, Johnson
Stoneham, Sara
Shamash, Jonathan
Joffe, Johnathan
Mazhar, Danish
Traill, Zoe
Ho, Ling-Pei
Brand, Sue
Protheroe, Andrew S.
author_sort Watson, Robert A.
collection PubMed
description Bleomycin, a cytotoxic chemotherapy agent, forms a key component of curative regimens for lymphoma and germ cell tumours. It can be associated with severe toxicity, long-term complications and even death in extreme cases. There is a lack of evidence or consensus on how to prevent and monitor bleomycin toxicity. We surveyed 63 germ cell cancer physicians from 32 cancer centres across the UK to understand their approach to using bleomycin. Subsequent guideline development was based upon current practice, best available published evidence and expert consensus. We observed heterogeneity in practice in the following areas: monitoring; route of administration; contraindications to use; baseline and follow-up investigations performed, and advice given to patients. A best-practice clinical guideline for the use of bleomycin in the treatment of germ cell tumours has been developed and includes recommendations regarding baseline investigations, the use of pulmonary function tests, route of administration, monitoring and patient advice. It is likely that existing heterogeneity in clinical practice of bleomycin prescribing has significant economic, safety and patient experience implications. The development of an evidence-based consensus guideline was supported by 93% of survey participants and aims to address these issues and homogenise practice across the UK.
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spelling pubmed-62194802019-10-25 Development of a best-practice clinical guideline for the use of bleomycin in the treatment of germ cell tumours in the UK Watson, Robert A. De La Peña, Hugo Tsakok, Maria T. Joseph, Johnson Stoneham, Sara Shamash, Jonathan Joffe, Johnathan Mazhar, Danish Traill, Zoe Ho, Ling-Pei Brand, Sue Protheroe, Andrew S. Br J Cancer Consensus Statement Bleomycin, a cytotoxic chemotherapy agent, forms a key component of curative regimens for lymphoma and germ cell tumours. It can be associated with severe toxicity, long-term complications and even death in extreme cases. There is a lack of evidence or consensus on how to prevent and monitor bleomycin toxicity. We surveyed 63 germ cell cancer physicians from 32 cancer centres across the UK to understand their approach to using bleomycin. Subsequent guideline development was based upon current practice, best available published evidence and expert consensus. We observed heterogeneity in practice in the following areas: monitoring; route of administration; contraindications to use; baseline and follow-up investigations performed, and advice given to patients. A best-practice clinical guideline for the use of bleomycin in the treatment of germ cell tumours has been developed and includes recommendations regarding baseline investigations, the use of pulmonary function tests, route of administration, monitoring and patient advice. It is likely that existing heterogeneity in clinical practice of bleomycin prescribing has significant economic, safety and patient experience implications. The development of an evidence-based consensus guideline was supported by 93% of survey participants and aims to address these issues and homogenise practice across the UK. Nature Publishing Group UK 2018-10-25 2018-10-30 /pmc/articles/PMC6219480/ /pubmed/30356125 http://dx.doi.org/10.1038/s41416-018-0300-x Text en © Cancer Research UK 2018 https://creativecommons.org/licenses/by/4.0/Note: This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0).
spellingShingle Consensus Statement
Watson, Robert A.
De La Peña, Hugo
Tsakok, Maria T.
Joseph, Johnson
Stoneham, Sara
Shamash, Jonathan
Joffe, Johnathan
Mazhar, Danish
Traill, Zoe
Ho, Ling-Pei
Brand, Sue
Protheroe, Andrew S.
Development of a best-practice clinical guideline for the use of bleomycin in the treatment of germ cell tumours in the UK
title Development of a best-practice clinical guideline for the use of bleomycin in the treatment of germ cell tumours in the UK
title_full Development of a best-practice clinical guideline for the use of bleomycin in the treatment of germ cell tumours in the UK
title_fullStr Development of a best-practice clinical guideline for the use of bleomycin in the treatment of germ cell tumours in the UK
title_full_unstemmed Development of a best-practice clinical guideline for the use of bleomycin in the treatment of germ cell tumours in the UK
title_short Development of a best-practice clinical guideline for the use of bleomycin in the treatment of germ cell tumours in the UK
title_sort development of a best-practice clinical guideline for the use of bleomycin in the treatment of germ cell tumours in the uk
topic Consensus Statement
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219480/
https://www.ncbi.nlm.nih.gov/pubmed/30356125
http://dx.doi.org/10.1038/s41416-018-0300-x
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