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177Lu-PSMA radioligand therapy of predominant lymph node metastatic prostate cancer.
von Eyben, Finn Edler; Singh, Aviral; Zhang, Jingjing; Nipsch, Karin; Meyrick, Danielle; Lenzo, Nat; Kairemo, Kalevi; Joensuu, Timo; Virgolini, Irene; Soydal, Cigdem; Kulkarni, Harshad R; Baum, Richard Paul.
Afiliação
  • von Eyben FE; Center of Tobacco Control Research, Odense, Denmark.
  • Singh A; Theranostics Center for Molecular Radiotherapy and Molecular Imaging, Zentralklinik Bad Berka, Bad Berka, Germany.
  • Zhang J; Theranostics Center for Molecular Radiotherapy and Molecular Imaging, Zentralklinik Bad Berka, Bad Berka, Germany.
  • Nipsch K; Theranostics Center for Molecular Radiotherapy and Molecular Imaging, Zentralklinik Bad Berka, Bad Berka, Germany.
  • Meyrick D; GenesisCare Oncology, Theranostics, East Freemantle, Australia.
  • Lenzo N; GenesisCare Oncology, Theranostics, East Freemantle, Australia.
  • Kairemo K; School of Medicine and Pharmacology, University of Western Australia, Nedlands, Australia.
  • Joensuu T; Docrates Cancer Center, Helsinki, Finland.
  • Virgolini I; Docrates Cancer Center, Helsinki, Finland.
  • Soydal C; Department of Nuclear Medicine, University Hospital in Innsbruck, Innsbruck, Austria.
  • Kulkarni HR; Department of Nuclear Medicine, University of Ankara, Faculty of Medicine, Universitesi Tip Faultesi Sikkiye, Ankara, Turkey.
  • Baum RP; Theranostics Center for Molecular Radiotherapy and Molecular Imaging, Zentralklinik Bad Berka, Bad Berka, Germany.
Oncotarget ; 10(25): 2451-2461, 2019 Mar 29.
Article em En | MEDLINE | ID: mdl-31069008
ABSTRACT
177Lu-PSMA radioligand therapy (LuPRLT) is mainly used for patients with metastatic castration-resistant prostate cancer who are resistant to established drugs. This study describes LuPRLT, either LuPSMA I&T or LuPSMA RLT-617, for 45 patients with predominant lymph node metastatic prostate cancer (LNM PC). Thirty-five patients had LNM and ten patients had LNM and one or two bone metastases. Before LuPRLT, the patients had prostate specific antigen (PSA) of median 18 µg/l (interquartile range (IQR) 3.3-39). LuPRLT was given with a cumulative injected 177Lu activity of median 14.5 GBq (IQR 12.2-20.4). Maximum percentage decline of PSA was median 92% (IQR 70-99). Thirty-five patients with only LNM had a better overall survival (OS) than ten patients with LNM and one or two bone metastases. Thirty-three docetaxel-naïve patients had a longer PSMA PET/CT progression-free survival than twelve patients who were resistant to docetaxel. Twenty-two patients who received LuPRLT with a cumulative injected 177Lu activity ≥ 14.8 GBq had a better PSMA PET/CT progression-free survival than 23 patients who received LuPRLT with a lower cumulative injected 177Lu activity. Seventeen patients with relapse after LuPRLT who received rechallenge LuPRLT or ActPRLT had a better OS than five patients who received other forms for relapse treatment. LuPRLT gave mild and transitory adverse effects. The findings of the present study suggest that LuPRLT of patients with LNM may be effective and safe. The promising results motivate randomized phase II trials to further quantify the impact of LuPRLT as treatment of patients with LNM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2019 Tipo de documento: Article