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. 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. RESULTS: Twenty-two patients with progressive/metastatic PGLs or...
Pheochromocytomas and paragangliomas (extra-adrenal pheochromocytomas) are relatively rare catechola...
Context: No therapies are approved for the treatment of metastatic and/or recurrent pheochromocytoma...
Paragangliomas (PGLs) are neuroendocrine tumors that arise embryologically from the neural crest. Sy...
Introduction. Peptide receptor radionuclide therapy (PRRT) with 177Lu-DOTATATE and 90Y-DOTATOC showe...
Pheochromocytoma and paraganglioma (PPGL) have currently only limited treatment options available fo...
Peptide receptor radiotherapy (PRRT) with 177Lu-DOTATATE has emerged as a promising therapy for neur...
There is little evidence to direct the management of malignant paragangliomas (mPGL) beyond initial ...
PURPOSE OF REVIEW: Pheochromocytomas and paragangliomas are rare tumors arising, respectively, from ...
Background: Phaeochromocytoma (phaeo) and paraganglioma (PGL) are rare conditions, which are maligna...
Malignant pheochromocytomas, a group of tumors that include metastatic paragangliomas, often produce...
Peptide receptor radionuclide therapy (PRRT) is used to treat patients with advanced malignant pheoc...
Introduction: Radionuclide therapy is a promising treatment modality in metastatic pheochromocytoma/...
AIM: Paragangliomas and pheochromocytomas are rare tumors arising from chromaffin cells. Approximate...
Paragangliomas (PGLs) are neuroendocrine tumors that arise embryologically from the neural crest. Sy...
Somatostatin receptor-targeting peptides are widely used for the imaging and therapy of neuroendocri...
Pheochromocytomas and paragangliomas (extra-adrenal pheochromocytomas) are relatively rare catechola...
Context: No therapies are approved for the treatment of metastatic and/or recurrent pheochromocytoma...
Paragangliomas (PGLs) are neuroendocrine tumors that arise embryologically from the neural crest. Sy...
Introduction. Peptide receptor radionuclide therapy (PRRT) with 177Lu-DOTATATE and 90Y-DOTATOC showe...
Pheochromocytoma and paraganglioma (PPGL) have currently only limited treatment options available fo...
Peptide receptor radiotherapy (PRRT) with 177Lu-DOTATATE has emerged as a promising therapy for neur...
There is little evidence to direct the management of malignant paragangliomas (mPGL) beyond initial ...
PURPOSE OF REVIEW: Pheochromocytomas and paragangliomas are rare tumors arising, respectively, from ...
Background: Phaeochromocytoma (phaeo) and paraganglioma (PGL) are rare conditions, which are maligna...
Malignant pheochromocytomas, a group of tumors that include metastatic paragangliomas, often produce...
Peptide receptor radionuclide therapy (PRRT) is used to treat patients with advanced malignant pheoc...
Introduction: Radionuclide therapy is a promising treatment modality in metastatic pheochromocytoma/...
AIM: Paragangliomas and pheochromocytomas are rare tumors arising from chromaffin cells. Approximate...
Paragangliomas (PGLs) are neuroendocrine tumors that arise embryologically from the neural crest. Sy...
Somatostatin receptor-targeting peptides are widely used for the imaging and therapy of neuroendocri...
Pheochromocytomas and paragangliomas (extra-adrenal pheochromocytomas) are relatively rare catechola...
Context: No therapies are approved for the treatment of metastatic and/or recurrent pheochromocytoma...
Paragangliomas (PGLs) are neuroendocrine tumors that arise embryologically from the neural crest. Sy...