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dc.contributor.authorMuselaers, CHJ
dc.contributor.authorBoers-Sonderen, MJ
dc.contributor.authorvan Oostenbrugge, TJ
dc.contributor.authorBoerman, OC
dc.contributor.authorDesar, IME
dc.contributor.authorStillebroer, AB
dc.contributor.authorMulder, SF
dc.contributor.authorvan Herpen, CML
dc.contributor.authorLangenhuijsen, JF
dc.contributor.authorOosterwijk, E
dc.contributor.authorOyen, WJG
dc.contributor.authorMulders, PFA
dc.date.accessioned2017-04-03T11:22:54Z
dc.date.issued2016-05
dc.identifier.citationEuropean urology, 2016, 69 (5), pp. 767 - 770
dc.identifier.issn0302-2838
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/554
dc.identifier.eissn1873-7560
dc.identifier.doi10.1016/j.eururo.2015.11.033
dc.description.abstractUnlabelled Despite advances in the treatment of metastatic clear cell renal cell carcinoma (ccRCC), there is still an unmet need in the treatment of this disease. A phase 2 radioimmunotherapy (RIT) trial with lutetium 177 ((177)Lu)-girentuximab was initiated to evaluate the efficacy of this approach. In this nonrandomized single-arm trial, patients with progressive metastatic ccRCC who met the inclusion criteria received 2405 MBq/m(2) of (177)Lu-girentuximab intravenously. In the absence of persistent toxicity and progressive disease, patients were eligible for retreatment after 3 mo with 75% of the previous activity dose. A total of 14 patients were included. After the first therapeutic infusion, eight patients (57%) had stable disease (SD) and one (7%) had a partial regression. The treatment was generally well tolerated but resulted in grade 3-4 myelotoxicity in most patients. After the second cycle, continued SD was observed in five of six patients, but none were eligible for retreatment due to prolonged thrombocytopenia. In conclusion, RIT with (177)Lu-girentuximab resulted in disease stabilization in 9 of 14 patients with progressive metastatic ccRCC, but myelotoxicity prevented retreatment in some patients.Patient summary We investigated the efficacy of lutetium 177-girentuximab radioimmunotherapy in patients with metastatic kidney cancer. The treatment resulted in disease stabilization in 9 of 14 patients. The main toxicity was prolonged low blood cell counts.Trial registration ClinicalTrials.gov identifier: NCT02002312 (https://clinicaltrials.gov/ct2/show/NCT02002312).
dc.formatPrint-Electronic
dc.format.extent767 - 770
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://www.rioxx.net/licenses/all-rights-reserved
dc.subjectHumans
dc.subjectCarcinoma, Renal Cell
dc.subjectKidney Neoplasms
dc.subjectThrombocytopenia
dc.subjectNeutropenia
dc.subjectLutetium
dc.subjectRadioisotopes
dc.subjectAntibodies, Monoclonal
dc.subjectDisease-Free Survival
dc.subjectRadioimmunotherapy
dc.subjectRetreatment
dc.subjectNon-Randomized Controlled Trials as Topic
dc.subjectCarbonic Anhydrase IX
dc.subjectAntineoplastic Agents, Immunological
dc.titlePhase 2 Study of Lutetium 177-Labeled Anti-Carbonic Anhydrase IX Monoclonal Antibody Girentuximab in Patients with Advanced Renal Cell Carcinoma.
dc.typeJournal Article
dcterms.dateAccepted2015-11-27
rioxxterms.versionofrecord10.1016/j.eururo.2015.11.033
rioxxterms.licenseref.urihttps://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2016-05
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfEuropean urology
pubs.issue5
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/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Translational Molecular Imaging
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/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Translational Molecular Imaging
pubs.publication-statusPublished
pubs.volume69
pubs.embargo.termsNot known
icr.researchteamTranslational Molecular Imagingen_US
dc.contributor.icrauthorOyen, Willem


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