نتایج جستجو برای: lu 177

تعداد نتایج: 19172  

2013
F. Guerriero M. E. Ferrari F. Botta F. Fioroni E. Grassi A. Versari A. Sarnelli M. Pacilio E. Amato L. Strigari L. Bodei G. Paganelli M. Iori G. Pedroli M. Cremonesi

Kidney dosimetry in (177)Lu and (90)Y PRRT requires 3 to 6 whole-body/SPECT scans to extrapolate the peptide kinetics, and it is considered time and resource consuming. We investigated the most adequate timing for imaging and time-activity interpolating curve, as well as the performance of a simplified dosimetry, by means of just 1-2 scans. Finally the influence of risk factors and of the pepti...

2016
Tobias Magnander Johanna Svensson Magnus Båth Peter Gjertsson Peter Bernhardt

The aims of this study were to determine how different background regions of interest (ROIs) around the kidney represent true background activity in over- and underlying tissues in (177)Lu-DOTA-octreatate ((177)Lu-DOTATATE) treatments and to determine the influence of the background positions on the kidney activity concentration estimates by the conjugate view (ConjV) and posterior view (PostV)...

Radioimmunotherapy (RIT) of Non-Hodgkin’s lymphoma (NHL) is said to be more advantageous compared to unlabelled therapeutic antibodies. To this date, radiolabelled murine anti-CD20 mAbs, Zevalin® and Bexxar® have been approved for imaging and therapy. A preparation containing rituximab, chimeric mAb radioimmunoconjugate suitable for Lu-177 labeling, could provide better imaging and therapeutic ...

Journal: :Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2004
Mark W Konijnenberg Magda Bijster Eric P Krenning Marion De Jong

UNLABELLED The therapeutic effects of peptide receptor-based radionuclide therapy are extensively being investigated in rats bearing tumors. Both the dose to the tumor and the therapy-limiting dose to normal tissues, such as kidneys and bone marrow, are of interest for these preclinical studies. The aim of this work was to develop a generalized computational model for internal dosimetry in rats...

2014
Mark W Konijnenberg Wout A P Breeman Erik de Blois Ho Sze Chan Otto C Boerman Peter Laverman Petra Kolenc-Peitl Marleen Melis Marion de Jong

BACKGROUND Targeted radionuclide therapy with high-energy beta-emitters is generally considered suboptimal to cure small tumours (<300 mg). Tumour targeting of the CCK2 receptor-binding minigastrin analogue PP-F11 was determined in a tumour-bearing mouse model at increasing peptide amounts. The optimal therapy was analysed for PP-F11 labelled with (90)Y, (177)Lu or (213)Bi, accounting for the r...

Journal: :Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2016
Richard P Baum Harshad R Kulkarni Christiane Schuchardt Aviral Singh Martina Wirtz Stefan Wiessalla Margret Schottelius Dirk Mueller Ingo Klette Hans-Jürgen Wester

UNLABELLED The objective of this study was to analyze the safety and efficacy of the (177)Lu-labeled DOTAGA-based prostate-specific membrane antigen (PSMA) ligand (177)Lu-DOTAGA-(I-y)fk(Sub-KuE) ((177)Lu-PSMA) in patients with metastatic castration-resistant prostate cancer (mCRPC). METHODS Fifty-six mCRPC patients underwent PSMA radioligand therapy (RLT) with (177)Lu-PSMA. (68)Ga-PSMA-(N,N'-...

2016
Eero Hippeläinen Mikko Tenhunen Hanna Mäenpää Antti Sohlberg

BACKGROUND In targeted radionuclide therapy (TRT), accurate quantification using SPECT/CT images is important for optimizing radiation dose delivered to both the tumour and healthy tissue. Quantitative SPECT images are regularly reconstructed using the ordered subset expectation maximization (OSEM) algorithm with various compensation methods such as attenuation (A), scatter (S) and detector and...

2016
Seval Beykan Jan S. Dam Uta Eberlein Jens Kaufmann Benedict Kjærgaard Lars Jødal Hakim Bouterfa Romain Bejot Michael Lassmann Svend Borup Jensen

BACKGROUND (177)Lu is used in peptide receptor radionuclide therapies for the treatment of neuroendocrine tumors. Based on the recent literature, SST2 antagonists are superior to agonists in tumor uptake. The compound OPS201 is the novel somatostatin antagonist showing the highest SST2 affinity. The aim of this study was to measure the in vivo biodistribution and dosimetry of (177)Lu-OPS201 in ...

2011
Chungen Pan Lifeng Cai Hong Lu Lu Lu Shibo Jiang

A novel chimeric protein-based HIV-1 fusion inhibitor targeting gp41 with high potency and stability Chungen Pan, Lifeng Cai, Hong Lu, Lu Lu, and Shibo Jiang* From Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065 MOE/MOH Key Laboratory of Medical Molecular Virology and Institute of Biomedical Sciences, Shanghai Medical College, Fudan University, Shanghai 200032,...

2009
Masanao Miwa Satoshi Honjo Petcharin Srivatanakul Lu Zeng Akihiro Ueda Chuanxu Jao Emi Ohta Takahiro Fujii Banchob Sripa Adisorn Jedpiyawongse Somyos Deerasamee Mantana Matharit Chutiwan Viwatthanasittiphong Dhiraphol Chenvidhya

Masanao Miwa, Satoshi Honjo, Petcharin Srivatanakul, Lu Zeng, Akihiro Ueda, Chuanxu Jao, Emi Ohta, Takahiro Fujii, Banchob Sripa, Adisorn Jedpiyawongse, Somyos Deerasamee, Mantana Matharit, Chutiwan Viwatthanasittiphong, Dhiraphol Chenvidhya, Masanao Miwa Bioscience, Nagahama Institute of Bio-Science and Technology, Japan, Fukuoka Hospital, National Hospital Organization, Japan, National Cancer...

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