Treatment of Malignant Pheochromocytomas With 131-I Metaiodobenzylguanidine and Chemotherapy
| Autor: | James C. Sisson, Shirley A. Zempel, Brahm Shapiro, Barry L. Shulkin, Susan A. Spaulding, Susan Urba |
|---|---|
| Rok vydání: | 1999 |
| Předmět: |
Adult
Male Cancer Research Vincristine medicine.medical_specialty Cyclophosphamide medicine.medical_treatment Dacarbazine Adrenal Gland Neoplasms Urology Pheochromocytoma chemistry.chemical_compound Antineoplastic Combined Chemotherapy Protocols medicine Humans Radionuclide Imaging Aged Chemotherapy business.industry Middle Aged medicine.disease Combined Modality Therapy Nitrogen mustard Surgery Radiation therapy 3-Iodobenzylguanidine Oncology chemistry Female Radiopharmaceuticals business Progressive disease medicine.drug |
| Zdroj: | American Journal of Clinical Oncology. 22:364-370 |
| ISSN: | 0277-3732 |
| DOI: | 10.1097/00000421-199908000-00008 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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