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Peptide Receptor Radionuclide Treatment and (131)I-MIBG in the management of patients with metastatic/progressive phaeochromocytomas and paragangliomas.

Authors :
Nastos K
Cheung VTF
Toumpanakis C
Navalkissoor S
Quigley AM
Caplin M
Khoo B
Source :
Journal of surgical oncology [J Surg Oncol] 2017 Mar; Vol. 115 (4), pp. 425-434. Date of Electronic Publication: 2017 Feb 06.
Publication Year :
2017

Abstract

Background and Objectives: Radionuclide therapy has been used to treat patients with progressive/metastatic paragangliomas (PGLs) and phaeochromocytomas (PCCs). The aim of the present study is to retrospectively compare the therapeutic outcomes of these modalities in patients with progressive/metastatic PCCs and PGLs.<br />Methods: Patients with progressive/metastatic PGLs and PCCs that were subjected to radionuclide treatment in our department were retrieved from our department's database for the period 1998-2013. Overall survival (OS), progression free survival (PFS), event free survival (EFS), and response to treatment were calculated. Treatment toxicity was documented.<br />Results: Twenty-two patients with progressive/metastatic PGLs or PCCs were treated with either (131)I-MIBG, (90)Y-DOTATATE or (177)Lu-DOTATATE. A total of 30 treatments were administered (16 treatments with (131)I-MIBG, 2 with (177)Lu-DOTATATE, and 12 with (90)Y-DOTATATE. Patients treated with PRRT had increased PFS and response to treatment compared to (131)I-MIBG treated patients (Pā€‰<ā€‰0.05). However, difference in OS was non significant (Pā€‰=ā€‰0.09). There was no difference in major toxicities between groups. When comparing only patients with PGLs, OS, PFS, EFS, and response to treatment were significantly higher in the PRRT treatment group.<br />Conclusion: PRRT treatment offers increased OS, PFS, EFS, and response to treatment compared to (131)I-MIBG therapy in patients with progressive/malignant PGLs.<br /> (© 2017 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1096-9098
Volume :
115
Issue :
4
Database :
MEDLINE
Journal :
Journal of surgical oncology
Publication Type :
Academic Journal
Accession number :
28166370
Full Text :
https://doi.org/10.1002/jso.24553