Abstract | PURPOSE: METHODS: Using multivariable-adjusted survival analyses and competing risk analyses we evaluated outcomes in patients with neuroendocrine tumor receiving (90)Y-DOTATOC, (177)Lu-DOTATOC or their combination. RESULTS: (90)Y-DOTATOC plus (177)Lu-DOTATOC treatment was associated with longer survival than (90)Y-DOTATOC (66.1 vs. 47.5 months; n = 1,358; p < 0.001) or (177)Lu-DOTATOC alone (66.1 vs. 45.5 months; n = 390; p < 0.001). (177)Lu-DOTATOC was associated with longer survival than (90)Y-DOTATOC in patients with solitary lesions (HR 0.3, range 0.1 - 0.7; n = 153; p = 0.005), extrahepatic metastases (HR 0.5, range 0.3 - 0.9; n = 256; p = 0.029) and metastases with low uptake (HR 0.1, range 0.05 - 0.4; n = 113; p = 0.001). (90)Y-DOTATOC induced higher hematotoxicity rates than combined treatment (9.5% vs. 4.0%, p = 0.005) or (177)Lu-DOTATOC (9.5 vs. 1.4%, p = 0.002). Renal toxicity was similar among the treatments. CONCLUSIONS:
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Authors | Piotr Radojewski, Rebecca Dumont, Nicolas Marincek, Philippe Brunner, Helmut R Mäcke, Jan Müller-Brand, Matthias Briel, Martin A Walter |
Journal | European journal of nuclear medicine and molecular imaging
(Eur J Nucl Med Mol Imaging)
Vol. 42
Issue 8
Pg. 1231-7
(Jul 2015)
ISSN: 1619-7089 [Electronic] Germany |
PMID | 25792454
(Publication Type: Evaluation Study, Journal Article)
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Chemical References |
- 177Lu-octreotide, DOTA(0)-Tyr(3)-
- Radiopharmaceuticals
- 90Y-octreotide, DOTA-Tyr(3)-
- Octreotide
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Female
- Humans
- Male
- Middle Aged
- Neuroendocrine Tumors
(radiotherapy)
- Octreotide
(administration & dosage, adverse effects, analogs & derivatives, therapeutic use)
- Radiopharmaceuticals
(administration & dosage, adverse effects, therapeutic use)
- Survival Analysis
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