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dc.contributor.authorBanerji, U
dc.contributor.authorWorkman, P
dc.date.accessioned2016-10-19T16:37:51Z
dc.date.issued2016-08-01
dc.identifier.citationSeminars in oncology, 2016, 43 (4), pp. 436 - 445
dc.identifier.issn0093-7754
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/181
dc.identifier.eissn1532-8708
dc.identifier.doi10.1053/j.seminoncol.2016.06.001
dc.description.abstractThe Pharmacological Audit Trail (PhAT) comprises a set of critical questions that need to be asked during discovery and development of an anticancer drug. Key aspects include: (1) defining a patient population; (2) establishing pharmacokinetic characteristics; (3) providing evidence of target engagement, pathway modulation, and biological effect with proof of concept pharmacodynamic biomarkers; (4) determining intermediate biomarkers of response; (5) assessing tumor response; and (6) determining how to overcome resistance by combination or sequential therapy and new target/drug discovery. The questions asked in the PhAT should be viewed as a continuum and not used in isolation. Different drug development programmes derive different types of benefit from these questions. The PhAT is critical in making go-no-go decisions in the development of currently studied drugs and will continue to be relevant to discovery and development of future generations of anticancer agents.
dc.formatPrint-Electronic
dc.format.extent436 - 445
dc.languageeng
dc.language.isoeng
dc.publisherW B SAUNDERS CO-ELSEVIER INC
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
dc.subjectHumans
dc.subjectNeoplasms
dc.subjectDNA Damage
dc.subjectNeovascularization, Pathologic
dc.subjectAntineoplastic Agents
dc.subjectPositron-Emission Tomography
dc.subjectTreatment Outcome
dc.subjectApoptosis
dc.subjectCell Proliferation
dc.subjectDrug Resistance, Neoplasm
dc.subjectPatient Selection
dc.subjectDrug Discovery
dc.subjectBiomarkers, Tumor
dc.titleCritical parameters in targeted drug development: the pharmacological audit trail.
dc.typeJournal Article
dcterms.dateAccepted2015-10-23
rioxxterms.versionofrecord10.1053/j.seminoncol.2016.06.001
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
rioxxterms.licenseref.startdate2016-08
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfSeminars in oncology
pubs.issue4
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Medicine Drug Development Unit (de Bono)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Pharmacology – Adaptive Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Medicine Drug Development Unit (de Bono)
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Medicine Drug Development Unit (de Bono)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Pharmacology – Adaptive Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Medicine Drug Development Unit (de Bono)
pubs.publication-statusPublished
pubs.volume43
pubs.embargo.termsNot known
icr.researchteamClinical Pharmacology – Adaptive Therapy
icr.researchteamMedicine Drug Development Unit (de Bono)
dc.contributor.icrauthorBanerji, Udai
dc.contributor.icrauthorWorkman, Paul


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