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dc.contributor.authorAndree, KC
dc.contributor.authorMentink, A
dc.contributor.authorZeune, LL
dc.contributor.authorTerstappen, LWMM
dc.contributor.authorStoecklein, NH
dc.contributor.authorNeves, RP
dc.contributor.authorDriemel, C
dc.contributor.authorLampignano, R
dc.contributor.authorYang, L
dc.contributor.authorNeubauer, H
dc.contributor.authorFehm, T
dc.contributor.authorFischer, JC
dc.contributor.authorRossi, E
dc.contributor.authorManicone, M
dc.contributor.authorBasso, U
dc.contributor.authorMarson, P
dc.contributor.authorZamarchi, R
dc.contributor.authorLoriot, Y
dc.contributor.authorLapierre, V
dc.contributor.authorFaugeroux, V
dc.contributor.authorOulhen, M
dc.contributor.authorFarace, F
dc.contributor.authorFowler, G
dc.contributor.authorSousa Fontes, M
dc.contributor.authorEbbs, B
dc.contributor.authorLambros, M
dc.contributor.authorCrespo, M
dc.contributor.authorFlohr, P
dc.contributor.authorde Bono, JS
dc.date.accessioned2020-11-10T11:29:51Z
dc.date.issued2018-11-15
dc.identifier.citationInternational journal of cancer, 2018, 143 (10), pp. 2584 - 2591
dc.identifier.issn0020-7136
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4219
dc.identifier.eissn1097-0215
dc.identifier.doi10.1002/ijc.31752
dc.description.abstractFrequently, the number of circulating tumor cells (CTC) isolated in 7.5 mL of blood is too small to reliably determine tumor heterogeneity and to be representative as a "liquid biopsy". In the EU FP7 program CTCTrap, we aimed to validate and optimize the recently introduced Diagnostic LeukApheresis (DLA) to screen liters of blood. Here we present the results obtained from 34 metastatic cancer patients subjected to DLA in the participating institutions. About 7.5 mL blood processed with CellSearch® was used as "gold standard" reference. DLAs were obtained from 22 metastatic prostate and 12 metastatic breast cancer patients at four different institutions without any noticeable side effects. DLA samples were prepared and processed with different analysis techniques. Processing DLA using CellSearch resulted in a 0-32 fold increase in CTC yield compared to processing 7.5 mL blood. Filtration of DLA through 5 μm pores microsieves was accompanied by large CTC losses. Leukocyte depletion of 18 mL followed by CellSearch yielded an increase of the number of CTC but a relative decrease in yield (37%) versus CellSearch DLA. In four out of seven patients with 0 CTC detected in 7.5 mL of blood, CTC were detected in DLA (range 1-4 CTC). The CTC obtained through DLA enables molecular characterization of the tumor. CTC enrichment technologies however still need to be improved to isolate all the CTC present in the DLA.
dc.formatPrint-Electronic
dc.format.extent2584 - 2591
dc.languageeng
dc.language.isoeng
dc.publisherWILEY
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0
dc.subjectHumans
dc.subjectBreast Neoplasms
dc.subjectLeukapheresis
dc.subjectFemale
dc.subjectMale
dc.subjectNeoplastic Cells, Circulating
dc.subjectProstatic Neoplasms, Castration-Resistant
dc.subjectLiquid Biopsy
dc.titleToward a real liquid biopsy in metastatic breast and prostate cancer: Diagnostic LeukApheresis increases CTC yields in a European prospective multicenter study (CTCTrap).
dc.typeJournal Article
dcterms.dateAccepted2018-06-25
rioxxterms.versionofrecord10.1002/ijc.31752
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc/4.0
rioxxterms.licenseref.startdate2018-11
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfInternational journal of cancer
pubs.issue10
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/Cancer Biomarkers
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Cancer Biomarkers
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Prostate Cancer Targeted Therapy Group
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/Cancer Biomarkers
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Cancer Biomarkers
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Prostate Cancer Targeted Therapy Group
pubs.publication-statusPublished
pubs.volume143
pubs.embargo.termsNot known
icr.researchteamCancer Biomarkers
icr.researchteamProstate Cancer Targeted Therapy Group
dc.contributor.icrauthorDe Bono, Johann


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Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc/4.0