نتایج جستجو برای: 177lu

تعداد نتایج: 759  

Journal: :Nuclear medicine review. Central & Eastern Europe 2013
Jolanta Kunikowska Adam Bajera Magdalena Sawicka Piotr Czwarnowski Bożena Pawłowicz Dariusz Aksamit Dariusz Pawlak Leszek Królicki

BACKGROUND Neuroendocrine tumors (NETs) are a heterogeneous group of neoplasms derived from endocrine stem cells.These tumors are characterized by overexpression of somatostatin receptors (SSTR), which is utilized for imaging using SSTR analogs. Peptide receptor radionuclide therapy (PRRT) somatostatin analogs labeled with 90Y and 177Lu in neuroendocrine tumors (NETs) results in symptomatic imp...

2017
In Ho Song Youn Noh Junhye Kwon Jae Ho Jung Byung Chul Lee Kwang Il Kim Yong Jin Lee Joo Hyun Kang Chae Seo Rhee Chul Hee Lee Tae Sup Lee Ik Joon Choi

The epidermal growth factor receptor (EGFR) is one of the most comprehensively studied molecular targets in head and neck squamous cell carcinoma (HNSCC). However, inherent and acquired resistance are serious problems and are responsible for limited clinical efficacy and tumor recurrence. In this study, we evaluated the feasibility of immuno-positron emission tomography (PET) imaging and radioi...

Journal: :Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2017
Anna-Karin Elf Peter Bernhardt Tobias Hofving Yvonne Arvidsson Eva Forssell-Aronsson Bo Wängberg Ola Nilsson Viktor Johanson

Neuroendocrine tumors (NETs) can be treated by peptide receptor radionuclide therapy using radiolabeled somatostatin analogs. However, the efficacy of such treatment is low and needs to be optimized. Our study evaluated the potential radiosensitizing effects of inhibition of nicotineamide phosphoribosyltransferase on 177Lu-DOTATATE treatment in a NET model. METHODS Nude mice xenografted with ...

2016
Nafise Salek Mojtaba Shamsaei Mohammad Ghannadi Maragheh Simindokht Shirvani Arani Ali Bahrami Samani

Skeletal uptake of radiolabeled-1, 4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetramethylene phosphoric acid (e.g., 177Lu-DOTMP) complex, is used for bone pain palliation. The moderate energy of β-emitting 177Lu (T½ = 6.7 d, Eβmax = 497keV) has been considered as a potential radionuclide for development of the bone-seeking radiopharmaceutical. Since the specific activity of the radiolabeled car...

Journal: :Molecular cancer therapeutics 2017
Ahmet Krasniqi Matthias D'Huyvetter Catarina Xavier Kevin Van der Jeught Serge Muyldermans José Van Der Heyden Tony Lahoutte Jan Tavernier Nick Devoogdt

Anti-CD20 radioimmunotherapy is an effective approach for therapy of relapsed or refractory CD20pos lymphomas, but faces limitations due to poor tumor penetration and undesirable pharmacokinetics of full antibodies. Camelid single-domain Ab fragments (sdAb) might circumvent some of the limitations of radiolabeled full antibodies. In this study, a set of hCD20-targeting sdAbs was generated, and ...

2014
Alexander H Staudacher Fares Al-Ejeh Cara K Fraser Jocelyn M Darby David M Roder Andrew Ruszkiewicz Jim Manavis Michael P Brown

BACKGROUND The lupus-associated (La)-specific murine monoclonal antibody DAB4 (APOMAB®) specifically binds dead cancer cells. Using DAB4, we examined La expression in human lung cancer samples to assess its suitability as a cancer-selective therapeutic target. We evaluated the safety and effectiveness of radioimmunotherapy (RIT) using DAB4 radiolabeled with Lutetium-177 (177Lu) in the murine Le...

2013
Amir Sabet James Nagarajah Ahmet Semih Dogan Hans-Jürgen Biersack Amin Sabet Stefan Guhlke Samer Ezziddin

BACKGROUND Peptide receptor radionuclide therapy (PRRT) with 177Lu-[DOTA0,Tyr3]octreotate (177Lu-octreotate) is generally performed using a fixed activity of 7.4 GBq (200 mCi) per course bound to 180 to 300 μg of the peptide. While this single activity may lead to suboptimal radiation doses in neuroendocrine tumors (NET) with advanced or bulky disease, dose escalation has been withheld due to c...

2017
Aurelie Maisonial-Besset Tiffany Witkowski Isabelle Navarro-Teulon Odile Berthier-Vergnes Giovanna Fois Yingying Zhu Sophie Besse Olivia Bawa Arnaud Briat Mercedes Quintana Alexandre Pichard Mathilde Bonnet Eric Rubinstein Jean-Pierre Pouget Paule Opolon Lydia Maigne Elisabeth Miot-Noirault Jean-Michel Chezal Claude Boucheix Françoise Degoul

Tetraspanin 8 (TSPAN8) overexpression is correlated with poor prognosis in human colorectal cancer (CRC). A murine mAb Ts29.2 specific for human TSPAN8 provided significant efficiency for immunotherapy in CRC pre-clinical models. We therefore evaluate the feasability of targeting TSPAN8 in CRC with radiolabeled Ts29.2. Staining of tissue micro-arrays with Ts29.2 revealed that TSPAN8 espression ...

2017
Libo Zhang Douglass C Vines Deborah A Scollard Trevor McKee Teesha Komal Milan Ganguly Trevor Do Bing Wu Natasha Alexander Reza Vali Amer Shammas Travis Besanger Sylvain Baruchel

Peptide-receptor imaging and therapy with radiolabeled somatostatin analogs such as 68Ga-DOTA-TATE and 177Lu-DOTA-TATE have become an effective treatment option for SSTR-positive neuroendocrine tumors. The purpose of this study was to evaluate the correlation of somatostatin receptor-2 (SSTR2) expression with 68Ga-DOTA-TATE uptake and 177Lu-DOTA-TATE therapy in neuroblastoma (NB) xenograft mode...

Journal: :Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2004
Anneli Schmitt Peter Bernhardt Ola Nilsson Håkan Ahlman Lars Kölby Helmut R Maecke Eva Forssell-Aronsson

UNLABELLED Small cell lung cancer (SCLC) is a tumor of neuroendocrine (NE) origin with very low survival rate. Somatostatin receptor scintigraphy using 111In-DTPA-octreotide (DTPA is diethylenetriaminepentaacetic acid) is a well-established method for the visualization of somatostatin receptor-expressing NE tumors. Recently, new combinations of radionuclides and somatostatin analogs have been i...

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