Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Helmut R. Mäcke"'
Publikováno v:
J Nucl Med
The objective of this study was to assess the safety, dosimetry, and efficacy of the (177)Lu-labeled somatostatin receptor (SSTR) antagonist DOTA-p-Cl-Phe-cyclo(d-Cys-Tyr-d-4-amino-Phe(carbamoyl)-Lys-Thr-Cys)d-Tyr-NH(2) ((177)Lu-DOTA-LM3) in patients
Autor:
Frank Rösch, Cristina Müller, Aviral Singh, Jingjing Zhang, Nicholas P. van der Meulen, HJ Wester, Theodosia Maina, Christiane Schuchardt, Richard P. Baum, Dirk Müller, Harshad R. Kulkarni, Helmut R. Mäcke
Publikováno v:
Seminars in Nuclear Medicine. 49:422-437
Precision oncology is being driven by rapid advances in novel diagnostics and therapeutic interventions, with treatments targeted to the needs of individual patients on the basis of genetic, biomarker, phenotypic, or psychosocial characteristics that
Publikováno v:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 61(6)
Targeting tumor-expressed receptors using selective molecules for diagnostic, therapeutic, or both diagnostic and therapeutic (theragnostic) purposes is a promising approach in oncologic applications. Such approaches have increased significantly over
Publikováno v:
Journal of Nuclear Medicine. 57:67S-72S
Imaging plays an important role in prostate cancer (PC), including accurate evaluation of the extent of disease, assessment of sites of recurrent disease, and monitoring of response to treatment. Molecular imaging techniques are among the novel devel
Autor:
Helmut R. Mäcke, Dominik Cordier, Adrian Merlo, Martin Sailer, Stefan Kneifel, Jan Müller-Brand, Luigi Mariani, Flavio Forrer
Complete surgical resection beyond tumor margins cannot be achieved in glioblastoma multiforme (GBM) because of infiltrative nature. In several cancers, neoadjuvant treatment has been implemented to reduce the risk of tumor cell spreading during rese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39a719f9f9a8e0516a39ca568f811dcf
http://doc.rero.ch/record/310762/files/11060_2010_Article_153.pdf
http://doc.rero.ch/record/310762/files/11060_2010_Article_153.pdf
Autor:
Flavio Forrer, Adrian Merlo, Alfred Morgenstern, Frank Bruchertseifer, Dominik Cordier, Helmut R. Mäcke
Publikováno v:
Swiss Medical Forum ‒ Schweizerisches Medizin-Forum.
Die diffusible Radiopeptid-Brachytherapie mit Betastrahlern ist effektiv, aber mit einer betrachtlichen Spat-Neurotoxizitat behaftet. Durch die Verwendung von Alphastrahlern kann diese wesentlich vermindert werden.
Autor:
Martin A. Walter, Piotr Radojewski, Jan Müller-Brand, Matthias Briel, Philippe Brunner, Rebecca A. Dumont, Nicolas Marincek, Helmut R. Mäcke
Publikováno v:
Eur J Nucl Med Mol Imaging
Radojewski, Piotr; Dumont, Rebecca; Marincek, Nicolas; Brunner, Philippe; Mäcke, Helmut R; Müller-Brand, Jan; Briel, Matthias; Walter, Martin Alexander (2015). Towards tailored radiopeptide therapy. European journal of nuclear medicine and molecular imaging, 42(8), pp. 1231-1237. Springer 10.1007/s00259-015-3030-9
Radojewski, Piotr; Dumont, Rebecca; Marincek, Nicolas; Brunner, Philippe; Mäcke, Helmut R; Müller-Brand, Jan; Briel, Matthias; Walter, Martin Alexander (2015). Towards tailored radiopeptide therapy. European journal of nuclear medicine and molecular imaging, 42(8), pp. 1231-1237. Springer 10.1007/s00259-015-3030-9
PURPOSE Somatostatin receptor-targeted radiopeptide therapy is commonly performed using single radioisotopes. We evaluated the benefits and harms of combining radioisotopes in radiopeptide therapy in patients with neuroendocrine tumor. METHODS Using
Publikováno v:
Nature Reviews Urology. 10:235-244
Gastrin releasing peptide (GRP) is a regulatory peptide that acts through its receptor (GRPR) to regulate physiological functions in various organs. GRPR is overexpressed in neoplastic cells of most prostate cancers and some renal cell cancers and in
Publikováno v:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 58(2)
There is recent in vitro and in vivo evidence that somatostatin receptor sst2 antagonists are better tools to target neuroendocrine tumors (NET) than sst2 agonists. Indeed, antagonists bind to a greater number of sst2 sites than agonists. Whether sst
Autor:
Philippe Brunner, Jan Müller-Brand, Helmut Rasch, Nicolas Marincek, Anna Imhof, Helmut R. Mäcke, Martin A. Walter, Christoph Rochlitz, Christian Schindler, Matthias Briel
Publikováno v:
J Clin Oncol
Purpose To investigate response, survival, and safety profile of the somatostatin-based radiopeptide 90yttrium-labeled tetraazacyclododecane-tetraacetic acid modified Tyr-octreotide ([90Y-DOTA]-TOC) in neuroendocrine cancers. Patients and Methods In