131I-Meta-Iodobenzylguanidine Therapy for Pheochromocytoma/Paraganglioma and Neuroblastoma

0Citations
Citations of this article
4Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Patients with malignant/metastatic pheochromocytoma/paraganglioma (PHEO/PG) benefit from 131I-meta-iodobenzylguanidine (131I-mIBG) treatment: symptomatic response is high, ranging between 75 and 90 %, biochemical response rate is 45–74 %, and morphologic response is 27–47 %. Nevertheless, complete response is low, ranging from 0 to 18 %, whereas 5-year survival ranges between 45 and 85 %. Patients with neuroblastomas (NB), after 131I-mIBG treatment, have 65 % 2-year overall survival. For the majority of adult patients with PHEO/PG or NB, a realistic goal is to stabilize disease, provide symptomatic relief, and elicit biochemical response. For younger patients with refractory or relapsing NB, already burdened by prior therapies, therapeutic 131I-mIBG is considered when other treatment options are ineffective. In the future, high-purity, carrier-free 131I-mIBG may be further used and assessed.

Cite

CITATION STYLE

APA

Ilias, I., & Meristoudis, G. (2017). 131I-Meta-Iodobenzylguanidine Therapy for Pheochromocytoma/Paraganglioma and Neuroblastoma. In Contemporary Endocrinology (pp. 401–409). Humana Press Inc. https://doi.org/10.1007/978-3-319-46038-3_19

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free