Bringing a genomic perspective to the safety of drug treatment in oncology [version 1; referees: 3 approved]

This article describes the clinical relevance of toxicity of therapies administered to patients with cancer, putting the patient, rather than disease, at the center of the evaluation of safety of anti-cancer therapy. Hence, the implications of adverse events are described from the patient perspectiv...

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Main Author: Federico Innocenti
Format: Article
Language:English
Published: F1000 Research Ltd 2017-03-01
Series:F1000Research
Subjects:
Online Access:https://f1000research.com/articles/6-385/v1
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author Federico Innocenti
author_facet Federico Innocenti
author_sort Federico Innocenti
collection DOAJ
description This article describes the clinical relevance of toxicity of therapies administered to patients with cancer, putting the patient, rather than disease, at the center of the evaluation of safety of anti-cancer therapy. Hence, the implications of adverse events are described from the patient perspective, focusing on the impact of patient safety on quality of life and efficacy of treatment. Issues revolving around other types of safety, such as financial toxicity, are also discussed. The role played by genetics in the assessment of a patient’s risk of adverse events is also discussed, both in relation to the potential of genomic research and in the context of current tools of fruition in clinical care.
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spelling doaj.art-6e999abdf8144f08970b189272ddedae2022-12-21T23:45:31ZengF1000 Research LtdF1000Research2046-14022017-03-01610.12688/f1000research.10475.111288Bringing a genomic perspective to the safety of drug treatment in oncology [version 1; referees: 3 approved]Federico Innocenti0Eshelman School of Pharmacy, Center for Pharmacogenomics and Individualized Therapy, Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USAThis article describes the clinical relevance of toxicity of therapies administered to patients with cancer, putting the patient, rather than disease, at the center of the evaluation of safety of anti-cancer therapy. Hence, the implications of adverse events are described from the patient perspective, focusing on the impact of patient safety on quality of life and efficacy of treatment. Issues revolving around other types of safety, such as financial toxicity, are also discussed. The role played by genetics in the assessment of a patient’s risk of adverse events is also discussed, both in relation to the potential of genomic research and in the context of current tools of fruition in clinical care.https://f1000research.com/articles/6-385/v1Cancer TherapeuticsGenomicsMedical GeneticsPharmacogenomicsToxicology
spellingShingle Federico Innocenti
Bringing a genomic perspective to the safety of drug treatment in oncology [version 1; referees: 3 approved]
F1000Research
Cancer Therapeutics
Genomics
Medical Genetics
Pharmacogenomics
Toxicology
title Bringing a genomic perspective to the safety of drug treatment in oncology [version 1; referees: 3 approved]
title_full Bringing a genomic perspective to the safety of drug treatment in oncology [version 1; referees: 3 approved]
title_fullStr Bringing a genomic perspective to the safety of drug treatment in oncology [version 1; referees: 3 approved]
title_full_unstemmed Bringing a genomic perspective to the safety of drug treatment in oncology [version 1; referees: 3 approved]
title_short Bringing a genomic perspective to the safety of drug treatment in oncology [version 1; referees: 3 approved]
title_sort bringing a genomic perspective to the safety of drug treatment in oncology version 1 referees 3 approved
topic Cancer Therapeutics
Genomics
Medical Genetics
Pharmacogenomics
Toxicology
url https://f1000research.com/articles/6-385/v1
work_keys_str_mv AT federicoinnocenti bringingagenomicperspectivetothesafetyofdrugtreatmentinoncologyversion1referees3approved