Successful Second-Line Metronomic Temozolomide in Metastatic Paraganglioma: Case Reports and Review of the Literature

Author:

Tena Isabel12,Gupta Garima2,Tajahuerce Marcos1,Benavent Marta3,Cifrián Manuel4,Falcon Alejandro3,Fonfria María2,Olmo Maribel del4,Reboll Rosa5,Conde Antonio1,Moreno Francisca4,Balaguer Julia4,Cañete Adela4,Palasí Rosana4,Bello Pilar4,Marco Alfredo4,Ponce José Luis4,Merino Juan Francisco4,Llombart Antonio5,Sanchez Alfredo1,Pacak Karel2

Affiliation:

1. Department of Medical Oncology, Castellon Provincial Hospital, Castellón, Spain

2. Section on Medical Neuroendocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA

3. Medical Oncology Department, Virgen del Rocío University Hospital, Seville, Spain

4. University Hospital La Fe, Valencia, Spain

5. Department of Medical Oncology, Arnau de Vilanova Hospital, Valencia, Spain

Abstract

Metastatic pheochromocytoma and paraganglioma (mPHEO/PGL) are frequently associated with succinate dehydrogenase B ( SDHB) mutations. Cyclophosphamide-dacarbazine-vincristine (CVD) regimen is recommended as standard chemotherapy for advanced mPHEO/PGL. There is limited evidence to support the role of metronomic schemes (MS) of chemotherapy in mPHEO/PGL treatment. We report 2 patients with SDHB-related mPGL who received a regimen consisting of MS temozolomide (TMZ) and high-dose lanreotide after progression on both CVD chemotherapy and high-dose lanreotide. Molecular profiling of the tumor tissue from both patients revealed hypermethylation of the O6-methylguanine-DNA-methyltransferase ( MGMT) promoter. In one patient, progression-free survival was 13 months and the second patient remained under treatment after 27 months of stabilization of metabolic response of his disease. Treatment was well tolerated, and adverse effects were virtually absent. A modification in the scheme of TMZ from standard schemes to MS is safe and feasible and can be considered in patients with progressive mPHEO/PGL refractory to dacarbazine in standard doses.

Publisher

SAGE Publications

Subject

Oncology

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