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dc.contributor.authorDemirkol, Mehmet Onur
dc.contributor.authorEsen, Bariş
dc.contributor.authorSeymen, Hülya
dc.contributor.authorŞen, Melis
dc.contributor.authorUçar, Burcu
dc.contributor.authorKurtuldu, Sevgilay
dc.contributor.authorMandel, Nil Molinas
dc.contributor.authorBavbek, Sevil
dc.contributor.authorFalay, Okan
dc.contributor.authorTilki, Derya
dc.contributor.authorEsen, Tarik
dc.date.accessioned2023-12-25T11:42:59Z
dc.date.available2023-12-25T11:42:59Z
dc.date.issued2023en_US
dc.identifier.citationDemirkol, M. O., Esen, B., Seymen, H., Şen, M., Uçar, B., Kurtuldu, S., ... & Esen, T. (2022). Radioligand Therapy With 177Lu-PSMA-I&T in Patients With Metastatic Prostate Cancer: Oncological Outcomes and Toxicity Profile. Clinical Nuclear Medicine, 10-1097.en_US
dc.identifier.issn03639762
dc.identifier.urihttps://doi.org/10.1097/RLU.0000000000004901
dc.identifier.urihttps://hdl.handle.net/20.500.12294/3999
dc.description.abstractIntroduction This study aimed to investigate the oncological outcomes and toxicity profile of 177Lu-PSMA-I&T radioligand therapy (RLT) in patients with metastatic castration-resistant prostate cancer (mCRPC), as well as our initial experience in metastatic hormone-sensitive prostate cancer (mHSPC). Patients and Methods A total of 38 consecutive patients with metastatic prostate cancer (33 mCRPC and 5 mHSPC) received 177Lu-PSMA-I&T RLT, with a median of 2 cycles per patient (range, 1-7). Response to RLT was evaluated based on prostate-specific antigen (PSA) changes and imaging response. Clinical progression-free survival and overall survival were used to report oncological outcomes. Toxicity was assessed using the Common Toxicity Criteria for Adverse Events criteria. Results In mCRPC, 22 (69%), 18 (56%), and 11 (34%) patients achieved any PSA decline, PSA response of 30%, and PSA response of 50%, respectively. The clinical progression-free survival and overall survival after the first cycle of RLT were 6.3 and 21.4 months, respectively. In mHSPC, 177Lu-PSMA-I&T RLT resulted in excellent PSA response (93.0%-99.9%) in all cases. Clinical progression and cancer-related mortality occurred in only 1 case. Toxicity profile was favorable in both mHSPC and mCRPC. Conclusions 177Lu-PSMA-I&T RLT demonstrated favorable PSA response (30%) in over half of the patients with mCRPC and excellent PSA response in all patients with mHSPC. Toxicity profile was favorable in both mHSPC and mCRPC settings. Further studies are needed to evaluate the role of 177Lu-PSMA-I&T RLT in the management of metastatic prostate cancer. © Wolters Kluwer Health, Inc. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherLippincott Williams and Wilkinsen_US
dc.relation.ispartofClinical Nuclear Medicineen_US
dc.identifier.doi10.1097/RLU.0000000000004901en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectProstate Canceren_US
dc.subjectMetastaticen_US
dc.subjectPSMAen_US
dc.subjectRadioligand Therapyen_US
dc.subjectLu-177-PSMA-I&Ten_US
dc.titleRadioligand Therapy With 177Lu-PSMA-I&T in Patients With Metastatic Prostate Cancer Oncological Outcomes and Toxicity Profileen_US
dc.typearticleen_US
dc.departmentMühendislik ve Mimarlık Fakültesi, Biyomedikal Mühendisliği Bölümüen_US
dc.authorid0000-0002-8540-7832en_US
dc.identifier.volume48en_US
dc.identifier.issue12en_US
dc.identifier.startpageE564en_US
dc.identifier.endpageE569en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.institutionauthorUçar, Burcu
dc.authorwosidJTO-2477-2023en_US
dc.authorscopusid56487383400en_US
dc.identifier.wosqualityQ1en_US
dc.identifier.wosWOS:001100827700002en_US
dc.identifier.scopus2-s2.0-85176495147en_US
dc.identifier.pmid37844332en_US


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