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177Lu-labeled MOv18 as compared to 131I- or 90Y-labeled MOv18 has the better therapeutic effect in eradication of alpha folate receptor-expressing tumor xenografts.
Nucl. Med. Biol. 36, 759-770 (2009)
The mouse monoclonal antibody MOv18, directed against the alpha-isoform of folate receptor (FR), was investigated to identify the optimal radioconjugate for radioimmunotherapy of minimal residual disease in ovarian cancer. Methods: Pharmacokinetics, biodistribution, long-term therapeutic efficacy and toxicity of MOv18, labeled with the beta-emitters I-131, Y-90 and Lu-177, were compared in a xenografted mouse model, composed by two cell lines, A431FR and A431MK, differing only for FR expression. Results: A shorter blood clearance and a higher tumor uptake were observed for Y-90- and Lu-177- compared to I-131-MOv18, and a shorter blood pharmacokinetics was recorded in A431FR-bearing animals. At equitoxic maximum tolerable doses, the general irradiation by I-131- and Y-90-MOv18 gives rise to strong targeted effects on A431FR and nontargeted effects on A431MK tumors, while Lu-177-MOv18 was able to eradicate small size tumor masses expressing the antigen of interest exerting only mild non-targeted effects. Conclusion: Lu-177-MOv18 at the maximal tolerated dose is the immunoradioconjugate with the best therapeutic window in experimental conditions of small tumor volume.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Times Cited
Scopus
Cited By
Cited By
Altmetric
2.419
0.900
17
25
Anmerkungen
Besondere Publikation
Auf Hompepage verbergern
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Ovarian cancer; Monoclonal antibody MOv18; Radioimmunotherapy; Radiometals; Folate Receptor; monoclonal-antibody MOV18; ovarian-cancer; nude-mice; colorectal-cancer; radioimmunotherapy; carcinoma; efficacy; binding; model; Y-90
Sprache
englisch
Veröffentlichungsjahr
2009
HGF-Berichtsjahr
2009
ISSN (print) / ISBN
0969-8051
e-ISSN
0969-8051
Zeitschrift
Nuclear Medicine and Biology
Quellenangaben
Band: 36,
Heft: 7,
Seiten: 759-770
Verlag
Elsevier
Verlagsort
New York
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Radiation Protection (ISS)
PSP-Element(e)
G-501100-007
Scopus ID
69249203546
PubMed ID
19720288
Erfassungsdatum
2009-10-09