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dc.contributor.authorYilmaz, Ebru
dc.contributor.authorEngin, Muege Nur
dc.contributor.authorOezkan, Zeynep Goezde
dc.contributor.authorKovan, Bilal
dc.contributor.authorBueyuekkaya, Fikret
dc.contributor.authorPoyanli, Arzu
dc.contributor.authorTuerkmen, Cueneyt
dc.date.accessioned2020-12-02T18:01:21Z
dc.date.available2020-12-02T18:01:21Z
dc.date.issued2020
dc.identifier.issn0143-3636
dc.identifier.issn1473-5628
dc.identifier.urihttps://doi.org/10.1097/MNM.0000000000001284
dc.identifier.urihttp://hdl.handle.net/11446/3583
dc.descriptionWOS: 000589817400004en_US
dc.descriptionPubMed: 32941405en_US
dc.description.abstractBackground Peptide receptor radionuclide therapy and selective internal radiation therapy are effective radionuclide therapy modalities for unresectable metastatic neuroendocrine tumor patients that cannot be controlled with somatostatin analogs. the present study is intended to evaluate the therapeutic efficacy and toxicity of the combined therapy of selective internal radiation therapy and peptide receptor radionuclide therapy and stand-alone selective internal radiation therapy in patients with neuroendocrine tumor, a liver-dominant disease. Methods This cohort consists of 27 patients with metastatic neuroendocrine tumor and liver-dominant disease. They were grouped as the patients who were treated with selective internal radiation therapy for unresectable liver metastasis (n = 15) and the patients who received a combination of selective internal radiation therapy and peptide receptor radionuclide therapy (n = 12) for hepatic and extrahepatic metastasis. Treatment efficacy and treatment-associated toxicity were retrospectively assessed in both groups. Results the objective treatment response and stable disease were found in 13 patients (86.6%) in the selective internal radiation therapy group and eight patients (66.6%) in the selective internal radiation therapy + peptide receptor radionuclide therapy group. the median overall survival rate was found to be 34.9 months, in the selective internal radiation therapy group and 67.5 months in the selective internal radiation therapy + peptide receptor radionuclide therapy group (P = 0.217). the median progression-free survival data was not reached, and the mean values of progression-free survival were 53.1 +/- 9.9 months in the selective internal radiation therapy group, and 27.2 +/- 5.9 months in the selective internal radiation therapy + peptide receptor radionuclide therapy group (P = 0.561). Temporary lymphopenia was the most common side effect. Grade 1-2 hepatotoxicity was observed to be 6.6% in the selective internal radiation therapy group, while it was not observed in selective internal radiation therapy + peptide receptor radionuclide therapy group. Conclusions in the neuroendocrine tumors with liver-dominant metastatic disease, personalized selective internal radiation therapy and peptide receptor radionuclide therapy and their combinations result in increased survival rates. Selective internal radiation therapy alone could be an effective treatment in patients with liver-limited and -dominant disease.en_US
dc.language.isodeuen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.identifier.doi10.1097/MNM.0000000000001284en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectLu-177-octreotateen_US
dc.subjectY-90 microspheresen_US
dc.subjectneuroendocrine tumorsen_US
dc.subjectpeptide receptor radionuclide therapyen_US
dc.subjectselective internal radiation therapyen_US
dc.titleY-90 selective internal radiation therapy and peptide receptor radionuclide therapy for the treatment of metastatic neuroendocrine tumors: combination or not?en_US
dc.typearticleen_US
dc.relation.journalNuclear Medicine Communicationsen_US
dc.departmentDBÜen_US
dc.identifier.issue12en_US
dc.identifier.volume41en_US
dc.identifier.startpage1242en_US
dc.identifier.endpage1249en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Yilmaz, Ebru; Engin, Muege Nur; Oezkan, Zeynep Goezde; Kovan, Bilal; Bueyuekkaya, Fikret; Tuerkmen, Cueneyt] Istanbul Univ, Istanbul Fac Med, Dept Nucl Med, Istanbul, Turkey; [Poyanli, Arzu] Istanbul Univ, Istanbul Fac Med, Dept Radiol, Istanbul, Turkey; [Basaran, Mert] Istanbul Univ, Istanbul Fac Med, Dept Med Oncol, Istanbul, Turkey; [Saglam, Sezer] Demiroglu Bilim Univ, Dept Med Oncol, Istanbul, Turkeyen_US


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