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Delayed adverse events in phase I trials of molecularly targeted and cytotoxic agents

BACKGROUND: Grade 3 and 4 adverse events (AEs) during cycle 1 are traditionally used for dose escalation decisions in Phase I oncology trials. With molecularly targeted agents (MTAs), assessment of lower grade AEs and those in later cycles is considered increasingly relevant. METHODS: We conducted a...

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Detalles Bibliográficos
Publicado en:Oncotarget
Autores principales: Jordan, Emma J., Spicer, James, Sarker, Debashis
Formato: Artigo
Lenguaje:Inglês
Publicado: Impact Journals LLC 2018
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6188052/
https://ncbi.nlm.nih.gov/pubmed/30338038
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.26104
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