Amifostine Protects Against Cisplatin-Induced Ototoxicity in Children With Average-Risk Medulloblastoma
To determine the role of amifostine as a protectant against cisplatin-induced ototoxicity in patients with average-risk (AR) medulloblastoma treated with craniospinal radiotherapy and four cycles of cisplatin-based, dose-intense chemotherapy and stem-cell rescue. The primary objective was to determi...
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creator | FOULADI, Maryam CHINTAGUMPALA, Murali HALE, Gregory A KASOW, Kimberly A MERCHANT, Thomas E MORRIS, Brannon KRASIN, Matthew KUN, Larry E BOYETT, James M GAJJAR, Amar ASHLEY, David KELLIE, Stewart GURURANGAN, Sridharan HASSALL, Tim GRONEWOLD, Lindsey STEWART, Clinton F WALLACE, Dana BRONISCER, Alberto |
description | To determine the role of amifostine as a protectant against cisplatin-induced ototoxicity in patients with average-risk (AR) medulloblastoma treated with craniospinal radiotherapy and four cycles of cisplatin-based, dose-intense chemotherapy and stem-cell rescue.
The primary objective was to determine whether, in patients with AR medulloblastoma (n = 62), amifostine would decrease the need for hearing aids (defined as >or= grade 3 ototoxicity in one ear) compared with a control group (n = 35), 1 year from initiating treatment. Ninety-seven patients received craniospinal irradiation (23.4 Gy) followed by 55.8 Gy to the primary tumor bed using three-dimensional conformal technique, and four cycles of high-dose cyclophosphamide (4,000 mg/m(2)/cycle), cisplatin (75 mg/m(2)/cycle), and vincristine (two 1.5 mg/m(2) doses/cycle) and stem-cell rescue. When used, amifostine (600 mg/m(2)/dose) was administered as a bolus immediately before and 3 hours into the cisplatin infusion.
The median age of the 97 patients was 8.7 years (range, 3.2 to 20.2 years). The study and control groups were similar in age and sex distribution. Amifostine was well-tolerated. One year after treatment initiation, 13 patients (37.1%) in the control group versus nine (14.5%; one-sided chi(2) test P = .005) of the amifostine-treated patients had at least grade 3 ototoxicity, requiring hearing aid in at least one ear.
Amifostine administered before and during the cisplatin infusion can significantly reduce the risk of severe ototoxicity in patients with AR medulloblastoma receiving dose-intense chemotherapy. |
doi_str_mv | 10.1200/JCO.2007.14.3974 |
format | Article |
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The primary objective was to determine whether, in patients with AR medulloblastoma (n = 62), amifostine would decrease the need for hearing aids (defined as >or= grade 3 ototoxicity in one ear) compared with a control group (n = 35), 1 year from initiating treatment. Ninety-seven patients received craniospinal irradiation (23.4 Gy) followed by 55.8 Gy to the primary tumor bed using three-dimensional conformal technique, and four cycles of high-dose cyclophosphamide (4,000 mg/m(2)/cycle), cisplatin (75 mg/m(2)/cycle), and vincristine (two 1.5 mg/m(2) doses/cycle) and stem-cell rescue. When used, amifostine (600 mg/m(2)/dose) was administered as a bolus immediately before and 3 hours into the cisplatin infusion.
The median age of the 97 patients was 8.7 years (range, 3.2 to 20.2 years). The study and control groups were similar in age and sex distribution. Amifostine was well-tolerated. One year after treatment initiation, 13 patients (37.1%) in the control group versus nine (14.5%; one-sided chi(2) test P = .005) of the amifostine-treated patients had at least grade 3 ototoxicity, requiring hearing aid in at least one ear.
Amifostine administered before and during the cisplatin infusion can significantly reduce the risk of severe ototoxicity in patients with AR medulloblastoma receiving dose-intense chemotherapy.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2007.14.3974</identifier><identifier>PMID: 18669462</identifier><language>eng</language><publisher>Baltimore, MD: American Society of Clinical Oncology</publisher><subject>Adolescent ; Adult ; Amifostine - adverse effects ; Amifostine - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Biological and medical sciences ; Cerebellar Neoplasms - drug therapy ; Cerebellar Neoplasms - radiotherapy ; Cerebellar Neoplasms - surgery ; Child ; Child, Preschool ; Cisplatin - administration & dosage ; Cranial Irradiation ; Cyclophosphamide - administration & dosage ; Disease-Free Survival ; Female ; Hearing Aids ; Hearing Loss - chemically induced ; Hearing Loss - prevention & control ; Hearing Loss - rehabilitation ; Humans ; Male ; Medical sciences ; Medulloblastoma - drug therapy ; Medulloblastoma - radiotherapy ; Medulloblastoma - surgery ; Neurology ; Prospective Studies ; Risk Assessment ; Stem Cell Transplantation ; Time Factors ; Treatment Outcome ; Tumors ; Tumors of the nervous system. Phacomatoses ; Vincristine - administration & dosage</subject><ispartof>Journal of clinical oncology, 2008-08, Vol.26 (22), p.3749-3755</ispartof><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-444e5c564040d540e9fe09309b5f724bae8295e753e667051420a2f59d74b1083</citedby><cites>FETCH-LOGICAL-c503t-444e5c564040d540e9fe09309b5f724bae8295e753e667051420a2f59d74b1083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3716,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20553442$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18669462$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FOULADI, Maryam</creatorcontrib><creatorcontrib>CHINTAGUMPALA, Murali</creatorcontrib><creatorcontrib>HALE, Gregory A</creatorcontrib><creatorcontrib>KASOW, Kimberly A</creatorcontrib><creatorcontrib>MERCHANT, Thomas E</creatorcontrib><creatorcontrib>MORRIS, Brannon</creatorcontrib><creatorcontrib>KRASIN, Matthew</creatorcontrib><creatorcontrib>KUN, Larry E</creatorcontrib><creatorcontrib>BOYETT, James M</creatorcontrib><creatorcontrib>GAJJAR, Amar</creatorcontrib><creatorcontrib>ASHLEY, David</creatorcontrib><creatorcontrib>KELLIE, Stewart</creatorcontrib><creatorcontrib>GURURANGAN, Sridharan</creatorcontrib><creatorcontrib>HASSALL, Tim</creatorcontrib><creatorcontrib>GRONEWOLD, Lindsey</creatorcontrib><creatorcontrib>STEWART, Clinton F</creatorcontrib><creatorcontrib>WALLACE, Dana</creatorcontrib><creatorcontrib>BRONISCER, Alberto</creatorcontrib><title>Amifostine Protects Against Cisplatin-Induced Ototoxicity in Children With Average-Risk Medulloblastoma</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>To determine the role of amifostine as a protectant against cisplatin-induced ototoxicity in patients with average-risk (AR) medulloblastoma treated with craniospinal radiotherapy and four cycles of cisplatin-based, dose-intense chemotherapy and stem-cell rescue.
The primary objective was to determine whether, in patients with AR medulloblastoma (n = 62), amifostine would decrease the need for hearing aids (defined as >or= grade 3 ototoxicity in one ear) compared with a control group (n = 35), 1 year from initiating treatment. Ninety-seven patients received craniospinal irradiation (23.4 Gy) followed by 55.8 Gy to the primary tumor bed using three-dimensional conformal technique, and four cycles of high-dose cyclophosphamide (4,000 mg/m(2)/cycle), cisplatin (75 mg/m(2)/cycle), and vincristine (two 1.5 mg/m(2) doses/cycle) and stem-cell rescue. When used, amifostine (600 mg/m(2)/dose) was administered as a bolus immediately before and 3 hours into the cisplatin infusion.
The median age of the 97 patients was 8.7 years (range, 3.2 to 20.2 years). The study and control groups were similar in age and sex distribution. Amifostine was well-tolerated. One year after treatment initiation, 13 patients (37.1%) in the control group versus nine (14.5%; one-sided chi(2) test P = .005) of the amifostine-treated patients had at least grade 3 ototoxicity, requiring hearing aid in at least one ear.
Amifostine administered before and during the cisplatin infusion can significantly reduce the risk of severe ototoxicity in patients with AR medulloblastoma receiving dose-intense chemotherapy.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Amifostine - adverse effects</subject><subject>Amifostine - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Biological and medical sciences</subject><subject>Cerebellar Neoplasms - drug therapy</subject><subject>Cerebellar Neoplasms - radiotherapy</subject><subject>Cerebellar Neoplasms - surgery</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cisplatin - administration & dosage</subject><subject>Cranial Irradiation</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Hearing Aids</subject><subject>Hearing Loss - chemically induced</subject><subject>Hearing Loss - prevention & control</subject><subject>Hearing Loss - rehabilitation</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medulloblastoma - drug therapy</subject><subject>Medulloblastoma - radiotherapy</subject><subject>Medulloblastoma - surgery</subject><subject>Neurology</subject><subject>Prospective Studies</subject><subject>Risk Assessment</subject><subject>Stem Cell Transplantation</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>Tumors of the nervous system. Phacomatoses</subject><subject>Vincristine - administration & dosage</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkEtv1DAUhS0EokNhzwp5g1hlev2Kkw3SKOJR1GoqBIKd5ThO4uLEI9tT6L8noxm1sLqL851zpQ-h1wTWhAJcfGm26-XKNeFrVkv-BK2IoLKQUoinaAWS0YJU7OcZepHSLQDhFRPP0RmpyrLmJV2hYTO5PqTsZotvYsjW5IQ3g3Zzyrhxaef1khWXc7c3tsPbHHL444zL99jNuBmd76Kd8Q-XR7y5s1EPtvjq0i98bbu996H1OuUw6ZfoWa99sq9O9xx9__jhW_O5uNp-umw2V4URwHLBObfCiJIDh05wsHVvoWZQt6KXlLfaVrQWVgpmy1KCIJyCpr2oO8lbAhU7R--Pu7t9O9nO2DlH7dUuuknHexW0U_8nsxvVEO4UFcAlq5cBOA6YGFKKtn_oElAH6WqRrg7SFeHqIH2pvPn352PhZHkB3p4AnYz2fdSzcemBoyAE4_zAvTtyoxvG3y5alSbt_TJL1a0JtFSUKiZ5zf4CDSqZIg</recordid><startdate>20080801</startdate><enddate>20080801</enddate><creator>FOULADI, Maryam</creator><creator>CHINTAGUMPALA, Murali</creator><creator>HALE, Gregory A</creator><creator>KASOW, Kimberly A</creator><creator>MERCHANT, Thomas E</creator><creator>MORRIS, Brannon</creator><creator>KRASIN, Matthew</creator><creator>KUN, Larry E</creator><creator>BOYETT, James M</creator><creator>GAJJAR, Amar</creator><creator>ASHLEY, David</creator><creator>KELLIE, Stewart</creator><creator>GURURANGAN, Sridharan</creator><creator>HASSALL, Tim</creator><creator>GRONEWOLD, Lindsey</creator><creator>STEWART, Clinton F</creator><creator>WALLACE, Dana</creator><creator>BRONISCER, Alberto</creator><general>American Society of Clinical Oncology</general><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><scope>5PM</scope></search><sort><creationdate>20080801</creationdate><title>Amifostine Protects Against Cisplatin-Induced Ototoxicity in Children With Average-Risk Medulloblastoma</title><author>FOULADI, Maryam ; CHINTAGUMPALA, Murali ; HALE, Gregory A ; KASOW, Kimberly A ; MERCHANT, Thomas E ; MORRIS, Brannon ; KRASIN, Matthew ; KUN, Larry E ; BOYETT, James M ; GAJJAR, Amar ; ASHLEY, David ; KELLIE, Stewart ; GURURANGAN, Sridharan ; HASSALL, Tim ; GRONEWOLD, Lindsey ; STEWART, Clinton F ; WALLACE, Dana ; BRONISCER, Alberto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-444e5c564040d540e9fe09309b5f724bae8295e753e667051420a2f59d74b1083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Amifostine - adverse effects</topic><topic>Amifostine - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Biological and medical sciences</topic><topic>Cerebellar Neoplasms - drug therapy</topic><topic>Cerebellar Neoplasms - radiotherapy</topic><topic>Cerebellar Neoplasms - surgery</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cisplatin - administration & dosage</topic><topic>Cranial Irradiation</topic><topic>Cyclophosphamide - administration & dosage</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Hearing Aids</topic><topic>Hearing Loss - chemically induced</topic><topic>Hearing Loss - prevention & control</topic><topic>Hearing Loss - rehabilitation</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medulloblastoma - drug therapy</topic><topic>Medulloblastoma - radiotherapy</topic><topic>Medulloblastoma - surgery</topic><topic>Neurology</topic><topic>Prospective Studies</topic><topic>Risk Assessment</topic><topic>Stem Cell Transplantation</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><topic>Tumors of the nervous system. Phacomatoses</topic><topic>Vincristine - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FOULADI, Maryam</creatorcontrib><creatorcontrib>CHINTAGUMPALA, Murali</creatorcontrib><creatorcontrib>HALE, Gregory A</creatorcontrib><creatorcontrib>KASOW, Kimberly A</creatorcontrib><creatorcontrib>MERCHANT, Thomas E</creatorcontrib><creatorcontrib>MORRIS, Brannon</creatorcontrib><creatorcontrib>KRASIN, Matthew</creatorcontrib><creatorcontrib>KUN, Larry E</creatorcontrib><creatorcontrib>BOYETT, James M</creatorcontrib><creatorcontrib>GAJJAR, Amar</creatorcontrib><creatorcontrib>ASHLEY, David</creatorcontrib><creatorcontrib>KELLIE, Stewart</creatorcontrib><creatorcontrib>GURURANGAN, Sridharan</creatorcontrib><creatorcontrib>HASSALL, Tim</creatorcontrib><creatorcontrib>GRONEWOLD, Lindsey</creatorcontrib><creatorcontrib>STEWART, Clinton F</creatorcontrib><creatorcontrib>WALLACE, Dana</creatorcontrib><creatorcontrib>BRONISCER, Alberto</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FOULADI, Maryam</au><au>CHINTAGUMPALA, Murali</au><au>HALE, Gregory A</au><au>KASOW, Kimberly A</au><au>MERCHANT, Thomas E</au><au>MORRIS, Brannon</au><au>KRASIN, Matthew</au><au>KUN, Larry E</au><au>BOYETT, James M</au><au>GAJJAR, Amar</au><au>ASHLEY, David</au><au>KELLIE, Stewart</au><au>GURURANGAN, Sridharan</au><au>HASSALL, Tim</au><au>GRONEWOLD, Lindsey</au><au>STEWART, Clinton F</au><au>WALLACE, Dana</au><au>BRONISCER, Alberto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amifostine Protects Against Cisplatin-Induced Ototoxicity in Children With Average-Risk Medulloblastoma</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2008-08-01</date><risdate>2008</risdate><volume>26</volume><issue>22</issue><spage>3749</spage><epage>3755</epage><pages>3749-3755</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>To determine the role of amifostine as a protectant against cisplatin-induced ototoxicity in patients with average-risk (AR) medulloblastoma treated with craniospinal radiotherapy and four cycles of cisplatin-based, dose-intense chemotherapy and stem-cell rescue.
The primary objective was to determine whether, in patients with AR medulloblastoma (n = 62), amifostine would decrease the need for hearing aids (defined as >or= grade 3 ototoxicity in one ear) compared with a control group (n = 35), 1 year from initiating treatment. Ninety-seven patients received craniospinal irradiation (23.4 Gy) followed by 55.8 Gy to the primary tumor bed using three-dimensional conformal technique, and four cycles of high-dose cyclophosphamide (4,000 mg/m(2)/cycle), cisplatin (75 mg/m(2)/cycle), and vincristine (two 1.5 mg/m(2) doses/cycle) and stem-cell rescue. When used, amifostine (600 mg/m(2)/dose) was administered as a bolus immediately before and 3 hours into the cisplatin infusion.
The median age of the 97 patients was 8.7 years (range, 3.2 to 20.2 years). The study and control groups were similar in age and sex distribution. Amifostine was well-tolerated. One year after treatment initiation, 13 patients (37.1%) in the control group versus nine (14.5%; one-sided chi(2) test P = .005) of the amifostine-treated patients had at least grade 3 ototoxicity, requiring hearing aid in at least one ear.
Amifostine administered before and during the cisplatin infusion can significantly reduce the risk of severe ototoxicity in patients with AR medulloblastoma receiving dose-intense chemotherapy.</abstract><cop>Baltimore, MD</cop><pub>American Society of Clinical Oncology</pub><pmid>18669462</pmid><doi>10.1200/JCO.2007.14.3974</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Society of Clinical Oncology Online Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Adolescent Adult Amifostine - adverse effects Amifostine - therapeutic use Antineoplastic Combined Chemotherapy Protocols - adverse effects Biological and medical sciences Cerebellar Neoplasms - drug therapy Cerebellar Neoplasms - radiotherapy Cerebellar Neoplasms - surgery Child Child, Preschool Cisplatin - administration & dosage Cranial Irradiation Cyclophosphamide - administration & dosage Disease-Free Survival Female Hearing Aids Hearing Loss - chemically induced Hearing Loss - prevention & control Hearing Loss - rehabilitation Humans Male Medical sciences Medulloblastoma - drug therapy Medulloblastoma - radiotherapy Medulloblastoma - surgery Neurology Prospective Studies Risk Assessment Stem Cell Transplantation Time Factors Treatment Outcome Tumors Tumors of the nervous system. Phacomatoses Vincristine - administration & dosage |
title | Amifostine Protects Against Cisplatin-Induced Ototoxicity in Children With Average-Risk Medulloblastoma |
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