Treatment of malignant pheochromocytomas with 131-I metaiodobenzylguanidine and chemotherapy

Malignant pheochromocytomas have exhibited partial responses to treatments with 131-I metaiodobenzylguanidine (MIBG) and with chemotherapy. The authors combined these two therapeutic methods to determine if beneficial effects from each would be additive. Patients with documented malignant pheochromo...

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Veröffentlicht in:American journal of clinical oncology 1999-08, Vol.22 (4), p.364-370
Hauptverfasser: SISSON, J. C, SHAPIRO, B, SHULKIN, B. L, URBA, S, ZEMPEL, S, SPAULDING, S
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container_issue 4
container_start_page 364
container_title American journal of clinical oncology
container_volume 22
creator SISSON, J. C
SHAPIRO, B
SHULKIN, B. L
URBA, S
ZEMPEL, S
SPAULDING, S
description Malignant pheochromocytomas have exhibited partial responses to treatments with 131-I metaiodobenzylguanidine (MIBG) and with chemotherapy. The authors combined these two therapeutic methods to determine if beneficial effects from each would be additive. Patients with documented malignant pheochromocytomas were recruited with the intent of administering 131-I MIBG in three substantial amounts of radioactivity at 3-month intervals followed by a year of chemotherapy in which cyclophosphamide, dacarbazine, and vincristine were to be given in 21-day cycles. Six patients entered the protocol. After the 131-I MIBG treatments, three patients manifested declines in the presence of tumor (smaller tumor volume or abnormalities on bone and 131-I MIBG scans) and the function of tumor (decreased rate of normetanephrine excretion as the major index). Two patients completed at least 9 months of chemotherapy and showed further reductions in the presence and function of tumors and were classified as having partial responses. Progressive disease afflicted three of the other four subjects. Even though toxicity was minimal from 131-I MIBG, it was sufficient to force reduction in the dosages or duration of chemotherapy. A combination of 131-I MIBG treatments and chemotherapy produced additive effects in reducing malignant pheochromocytomas. Toxicity moderately curtailed the proposed chemotherapy protocol.
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Drug treatments</topic><topic>Pheochromocytoma - diagnostic imaging</topic><topic>Pheochromocytoma - drug therapy</topic><topic>Pheochromocytoma - radiotherapy</topic><topic>Pheochromocytoma - secondary</topic><topic>Radionuclide Imaging</topic><topic>Radiopharmaceuticals - therapeutic use</topic><topic>Vincristine - administration &amp; dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SISSON, J. C</creatorcontrib><creatorcontrib>SHAPIRO, B</creatorcontrib><creatorcontrib>SHULKIN, B. 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subjects 3-Iodobenzylguanidine - therapeutic use
Adrenal Gland Neoplasms - diagnostic imaging
Adrenal Gland Neoplasms - drug therapy
Adrenal Gland Neoplasms - pathology
Adrenal Gland Neoplasms - radiotherapy
Adult
Aged
Antineoplastic agents
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Combined Modality Therapy
Combined treatments (chemotherapy of immunotherapy associated with an other treatment)
Cyclophosphamide - administration & dosage
Dacarbazine - administration & dosage
Female
Humans
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
Pheochromocytoma - diagnostic imaging
Pheochromocytoma - drug therapy
Pheochromocytoma - radiotherapy
Pheochromocytoma - secondary
Radionuclide Imaging
Radiopharmaceuticals - therapeutic use
Vincristine - administration & dosage
title Treatment of malignant pheochromocytomas with 131-I metaiodobenzylguanidine and chemotherapy
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