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 |
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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. |
doi_str_mv | 10.1097/00000421-199908000-00008 |
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C ; SHAPIRO, B ; SHULKIN, B. L ; URBA, S ; ZEMPEL, S ; SPAULDING, S</creator><creatorcontrib>SISSON, J. C ; SHAPIRO, B ; SHULKIN, B. L ; URBA, S ; ZEMPEL, S ; SPAULDING, S</creatorcontrib><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.</description><identifier>ISSN: 0277-3732</identifier><identifier>EISSN: 1537-453X</identifier><identifier>DOI: 10.1097/00000421-199908000-00008</identifier><identifier>PMID: 10440191</identifier><identifier>CODEN: AJCODI</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>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</subject><ispartof>American journal of clinical oncology, 1999-08, Vol.22 (4), p.364-370</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-b1f4127b05c505ccfdfd756cf10bc65e71ffa9d606369f1a68fbb3213335791e3</citedby><cites>FETCH-LOGICAL-c340t-b1f4127b05c505ccfdfd756cf10bc65e71ffa9d606369f1a68fbb3213335791e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1925581$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10440191$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SISSON, J. C</creatorcontrib><creatorcontrib>SHAPIRO, B</creatorcontrib><creatorcontrib>SHULKIN, B. L</creatorcontrib><creatorcontrib>URBA, S</creatorcontrib><creatorcontrib>ZEMPEL, S</creatorcontrib><creatorcontrib>SPAULDING, S</creatorcontrib><title>Treatment of malignant pheochromocytomas with 131-I metaiodobenzylguanidine and chemotherapy</title><title>American journal of clinical oncology</title><addtitle>Am J Clin Oncol</addtitle><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.</description><subject>3-Iodobenzylguanidine - therapeutic use</subject><subject>Adrenal Gland Neoplasms - diagnostic imaging</subject><subject>Adrenal Gland Neoplasms - drug therapy</subject><subject>Adrenal Gland Neoplasms - pathology</subject><subject>Adrenal Gland Neoplasms - radiotherapy</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Combined Modality Therapy</subject><subject>Combined treatments (chemotherapy of immunotherapy associated with an other treatment)</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Dacarbazine - administration & dosage</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Pheochromocytoma - diagnostic imaging</subject><subject>Pheochromocytoma - drug therapy</subject><subject>Pheochromocytoma - radiotherapy</subject><subject>Pheochromocytoma - secondary</subject><subject>Radionuclide Imaging</subject><subject>Radiopharmaceuticals - therapeutic use</subject><subject>Vincristine - administration & dosage</subject><issn>0277-3732</issn><issn>1537-453X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkEtLxDAUhYMozjj6FyQLt9HcpmmapQw-BgbcjOBCKGmaTCtNU5KK1F9vxxkfFy6Xc_jOXRyEMNBroFLc0N2kCRCQUtJ8EmTn5EdoDpwJknL2cozmNBGCMMGSGTqL8W0ieEbFKZoBTVMKEubodROMGpzpBuwtdqpttp2aRF8br-vgndfj4J2K-KMZagwMyAo7M6jGV7403efYbt9V11RNZ7DqKqxr4_xQm6D68RydWNVGc3G4C_R8f7dZPpL108NqebsmmqV0ICXYFBJRUq75tNpWthI80xZoqTNuBFirZJXRjGXSgspyW5YsAcYYFxIMW6B8_1cHH2MwtuhD41QYC6DFrrDip7Dit7BvK5-il_to_146U_0L7huagKsDoKJWrQ2q003842TCeQ7sC9X-dGo</recordid><startdate>19990801</startdate><enddate>19990801</enddate><creator>SISSON, J. C</creator><creator>SHAPIRO, B</creator><creator>SHULKIN, B. L</creator><creator>URBA, S</creator><creator>ZEMPEL, S</creator><creator>SPAULDING, S</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19990801</creationdate><title>Treatment of malignant pheochromocytomas with 131-I metaiodobenzylguanidine and chemotherapy</title><author>SISSON, J. C ; SHAPIRO, B ; SHULKIN, B. L ; URBA, S ; ZEMPEL, S ; SPAULDING, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-b1f4127b05c505ccfdfd756cf10bc65e71ffa9d606369f1a68fbb3213335791e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>3-Iodobenzylguanidine - therapeutic use</topic><topic>Adrenal Gland Neoplasms - diagnostic imaging</topic><topic>Adrenal Gland Neoplasms - drug therapy</topic><topic>Adrenal Gland Neoplasms - pathology</topic><topic>Adrenal Gland Neoplasms - radiotherapy</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Combined Modality Therapy</topic><topic>Combined treatments (chemotherapy of immunotherapy associated with an other treatment)</topic><topic>Cyclophosphamide - administration & dosage</topic><topic>Dacarbazine - administration & dosage</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. 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 & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SISSON, J. C</creatorcontrib><creatorcontrib>SHAPIRO, B</creatorcontrib><creatorcontrib>SHULKIN, B. L</creatorcontrib><creatorcontrib>URBA, S</creatorcontrib><creatorcontrib>ZEMPEL, S</creatorcontrib><creatorcontrib>SPAULDING, S</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>American journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SISSON, J. C</au><au>SHAPIRO, B</au><au>SHULKIN, B. L</au><au>URBA, S</au><au>ZEMPEL, S</au><au>SPAULDING, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment of malignant pheochromocytomas with 131-I metaiodobenzylguanidine and chemotherapy</atitle><jtitle>American journal of clinical oncology</jtitle><addtitle>Am J Clin Oncol</addtitle><date>1999-08-01</date><risdate>1999</risdate><volume>22</volume><issue>4</issue><spage>364</spage><epage>370</epage><pages>364-370</pages><issn>0277-3732</issn><eissn>1537-453X</eissn><coden>AJCODI</coden><abstract>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.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>10440191</pmid><doi>10.1097/00000421-199908000-00008</doi><tpages>7</tpages></addata></record> |
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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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