Journal article
High-Specific-Activity- 131 I-MIBG versus 177 Lu-DOTATATE Targeted Radionuclide Therapy for Metastatic Pheochromocytoma and Paraganglioma
Clinical cancer research, Vol.27(11), pp.2989-2995
06/01/2021
DOI: 10.1158/1078-0432.CCR-20-3703
PMCID: PMC8172462
PMID: 33685867
Abstract
Targeted radionuclide therapies (TRT) using
I-metaiodobenzylguanidine (
I-MIBG) and peptide receptor radionuclide therapy (
Lu or
Y) represent several of the therapeutic options in the management of metastatic/inoperable pheochromocytoma/paraganglioma. Recently, high-specific-activity-
I-MIBG therapy was approved by the FDA and both
Lu-DOTATATE and
I-MIBG therapy were recommended by the National Comprehensive Cancer Network guidelines for the treatment of metastatic pheochromocytoma/paraganglioma. However, a clinical dilemma often arises in the selection of TRT, especially when a patient can be treated with either type of therapy based on eligibility by MIBG and somatostatin receptor imaging. To address this problem, we assembled a group of international experts, including oncologists, endocrinologists, and nuclear medicine physicians, with substantial experience in treating neuroendocrine tumors with TRTs to develop consensus and provide expert recommendations and perspectives on how to select between these two therapeutic options for metastatic/inoperable pheochromocytoma/paraganglioma. This article aims to summarize the survival outcomes of the available TRTs; discuss personalized treatment strategies based on functional imaging scans; address practical issues, including regulatory approvals; and compare toxicities and risk factors across treatments. Furthermore, it discusses the emerging TRTs.
Details
- Title: Subtitle
- High-Specific-Activity- 131 I-MIBG versus 177 Lu-DOTATATE Targeted Radionuclide Therapy for Metastatic Pheochromocytoma and Paraganglioma
- Creators
- Abhishek Jha - Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentDavid Taïeb - Aix-Marseille UniversitéJorge A Carrasquillo - Memorial Sloan Kettering Cancer CenterDaniel A Pryma - University of PennsylvaniaMayank Patel - Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentCorina Millo - National Institutes of HealthWouter W de Herder - Erasmus MC Cancer InstituteJaydira Del Rivero - Center for Cancer ResearchJoakim Crona - Uppsala UniversityBarry L Shulkin - St. Jude Children's Research HospitalIrene Virgolini - Innsbruck Medical UniversityAlice P Chen - Division of Cancer Treatment and Diagnosis, NCI, NIH, Bethesda, Maryland.Bhagwant R Mittal - Post Graduate Institute of Medical Education and ResearchSandip Basu - Homi Bhabha National InstituteJoseph S Dillon - University of Iowa Hospitals and ClinicsThomas A Hope - University of California, San FranciscoCarina Mari Aparici - Stanford University School of MedicineAndrei H Iagaru - Stanford UniversityRodney J Hicks - The University of MelbourneAnca M Avram - University of MichiganJonathan R Strosberg - Moffitt Cancer CenterAli Cahid Civelek - Johns Hopkins UniversityFrank I Lin - National Institutes of HealthNeeta Pandit-Taskar - Memorial Sloan Kettering Cancer CenterKarel Pacak - Eunice Kennedy Shriver National Institute of Child Health and Human Development
- Resource Type
- Journal article
- Publication Details
- Clinical cancer research, Vol.27(11), pp.2989-2995
- DOI
- 10.1158/1078-0432.CCR-20-3703
- PMID
- 33685867
- PMCID
- PMC8172462
- NLM abbreviation
- Clin Cancer Res
- ISSN
- 1078-0432
- eISSN
- 1557-3265
- Grant note
- P30 CA008748 / NCI NIH HHS Z01 HD008735 / Intramural NIH HHS P30 CA086862 / NCI NIH HHS
- Language
- English
- Date published
- 06/01/2021
- Academic Unit
- Fraternal Order of Eagles Diabetes Research Center; Endocrinology and Metabolism; Internal Medicine
- Record Identifier
- 9984359866402771
Metrics
14 Record Views