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  3. Survival after somatostatin based radiopeptide therapy with (90)Y-DOTATOC vs. (90)Y-DOTATOC plus (177)Lu-DOTATOC in metastasized gastrinoma.
 

Survival after somatostatin based radiopeptide therapy with (90)Y-DOTATOC vs. (90)Y-DOTATOC plus (177)Lu-DOTATOC in metastasized gastrinoma.

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BORIS DOI
10.7892/boris.67183
Date of Publication
2015
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Dumont, Rebecca A
Seiler, Daniela
Marincek, Nicolas
Universitätsklinik für Nuklearmedizin
Brunner, Philippe
Radojewski, Piotr
Universitätsklinik für Nuklearmedizin
Rochlitz, Christoph
Müller-Brand, Jan
Maecke, Helmut R
Briel, Matthias
Walter, Martin Alexanderorcid-logo
Universitätsklinik für Nuklearmedizin
Subject(s)

600 - Technology::610...

Series
American journal of nuclear medicine and molecular imaging
ISSN or ISBN (if monograph)
2160-8407
Language
English
PubMed ID
25625026
Uncontrolled Keywords

Yttrium

gastrinoma

lutetium

somatostatin

survival

Description
We aimed to explore the effects of (90)Y-DOTATOC and (90)Y-DOTATOC plus (177)Lu-DOTATOC on survival of patients with metastasized gastrinoma. Patients with progressive metastasized gastrinoma were treated with repeated cycles of (90)Y-DOTATOC or with cycles alternating between (90)Y-DOTATOC and (177)Lu-DOTATOC until tumor progression or permanent toxicity. Multivariable Cox regression analyses were used to study predictors of survival. A total of 36 patients were enrolled; 30 patients received (90)Y-DOTATOC (median activity per patient 11.8GBq; range: 6.1-62.2GBq) and 6 patients received (90)Y-DOTATOC plus (177)Lu-DOTATOC (median activity per patient: 14.8GBq; range: 7.4-14.8GBq). Response was found in 26 patients (72.2%), including morphological (n=12, 33.3%), biochemical (n=14, 38.9%) and/or clinical response (n=6, 16.2%). A total of 21 patients (58.3%) experienced hematotoxicity grade 1/2, while 1 patient (2.8%) experienced hematotoxicity grade 3; no grade 4 hematotoxicity occurred. Furthermore, 2 patients (5.6%) developed grade 4 renal toxicity; no grade 5 renal toxicity occurred. Responders had a significantly longer median survival from time of enrollment than non-responders (45.1 months, range: 37.1-53.1 months vs. 12.6 months, range: 11.0-14.2, hazard ratio: 0.12 (0.027-0.52), p=0.005). Additionally, there was a trend towards longer median survival with (90)Y-DOTATOC plus (177)Lu-DOTATOC as compared to (90)Y-DOTATOC alone (60.2 months, range: 19.8-100.6 months vs. 27.0 months, range: 4.0-50.0, hazard ratio: 0.21 (0.01-3.98), p=0.16). Response to (90)Y-DOTATOC and (90)Y-DOTATOC plus (177)Lu-DOTATOC therapy is associated with a longer survival in patients with metastasized gastrinoma. Both treatment regimens are promising tools for management of progressive gastrinoma.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/132184
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ajnmmi0002037.pdftextAdobe PDF966.31 KBAttribution-NonCommercial (CC BY-NC 4.0)publishedOpen
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