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dc.contributor.authorCollins, DC
dc.contributor.authorSundar, R
dc.contributor.authorLim, JSJ
dc.contributor.authorYap, TA
dc.date.accessioned2017-03-02T16:58:15Z
dc.date.issued2017-01
dc.identifier.citationTrends in pharmacological sciences, 2017, 38 (1), pp. 25 - 40
dc.identifier.issn0165-6147
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/468
dc.identifier.eissn1873-3735
dc.identifier.doi10.1016/j.tips.2016.10.012
dc.description.abstractPrecision medicine continues to be the benchmark to which we strive in cancer research. Seeking out actionable aberrations that can be selectively targeted by drug compounds promises to optimize treatment efficacy and minimize toxicity. Utilizing these different targeted agents in combination or in sequence may further delay resistance to treatments and prolong antitumor responses. Remarkable progress in the field of immunotherapy adds another layer of complexity to the management of cancer patients. Corresponding advances in companion biomarker development, novel methods of serial tumor assessments, and innovative trial designs act synergistically to further precision medicine. Ongoing hurdles such as clonal evolution, intra- and intertumor heterogeneity, and varied mechanisms of drug resistance continue to be challenges to overcome. Large-scale data-sharing and collaborative networks using next-generation sequencing (NGS) platforms promise to take us further into the cancer 'ome' than ever before, with the goal of achieving successful precision medicine.
dc.formatPrint-Electronic
dc.format.extent25 - 40
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://www.rioxx.net/licenses/all-rights-reserved
dc.subjectHumans
dc.subjectNeoplasms
dc.subjectBiopsy
dc.subjectImmunotherapy
dc.subjectDrug Resistance, Neoplasm
dc.subjectClinical Trials as Topic
dc.subjectHigh-Throughput Nucleotide Sequencing
dc.subjectBiomarkers, Tumor
dc.subjectPrecision Medicine
dc.titleTowards Precision Medicine in the Clinic: From Biomarker Discovery to Novel Therapeutics.
dc.typeJournal Article
dcterms.dateAccepted2016-10-19
rioxxterms.versionofrecord10.1016/j.tips.2016.10.012
rioxxterms.licenseref.urihttps://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2017-01
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfTrends in pharmacological sciences
pubs.issue1
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/Medicine Drug Development Unit (de Bono)
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
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/Medicine Drug Development Unit (de Bono)
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume38
pubs.embargo.termsNot known
icr.researchteamMedicine Drug Development Unit (de Bono)en_US
dc.contributor.icrauthorYap, Timothy
dc.contributor.icrauthorMarsden,


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