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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of clinical oncology 2008-08, Vol.26 (22), p.3749-3755
Hauptverfasser: 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
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3755
container_issue 22
container_start_page 3749
container_title Journal of clinical oncology
container_volume 26
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
fullrecord <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2504739</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>18669462</sourcerecordid><originalsourceid>FETCH-LOGICAL-c503t-444e5c564040d540e9fe09309b5f724bae8295e753e667051420a2f59d74b1083</originalsourceid><addsrcrecordid>eNpVkEtv1DAUhS0EokNhzwp5g1hlev2Kkw3SKOJR1GoqBIKd5ThO4uLEI9tT6L8noxm1sLqL851zpQ-h1wTWhAJcfGm26-XKNeFrVkv-BK2IoLKQUoinaAWS0YJU7OcZepHSLQDhFRPP0RmpyrLmJV2hYTO5PqTsZotvYsjW5IQ3g3Zzyrhxaef1khWXc7c3tsPbHHL444zL99jNuBmd76Kd8Q-XR7y5s1EPtvjq0i98bbu996H1OuUw6ZfoWa99sq9O9xx9__jhW_O5uNp-umw2V4URwHLBObfCiJIDh05wsHVvoWZQt6KXlLfaVrQWVgpmy1KCIJyCpr2oO8lbAhU7R--Pu7t9O9nO2DlH7dUuuknHexW0U_8nsxvVEO4UFcAlq5cBOA6YGFKKtn_oElAH6WqRrg7SFeHqIH2pvPn352PhZHkB3p4AnYz2fdSzcemBoyAE4_zAvTtyoxvG3y5alSbt_TJL1a0JtFSUKiZ5zf4CDSqZIg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Amifostine Protects Against Cisplatin-Induced Ototoxicity in Children With Average-Risk Medulloblastoma</title><source>MEDLINE</source><source>American Society of Clinical Oncology Online Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><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</creator><creatorcontrib>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</creatorcontrib><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 &gt;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 &amp; dosage ; Cranial Irradiation ; Cyclophosphamide - administration &amp; dosage ; Disease-Free Survival ; Female ; Hearing Aids ; Hearing Loss - chemically induced ; Hearing Loss - prevention &amp; 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 &amp; 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&amp;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 &gt;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 &amp; dosage</subject><subject>Cranial Irradiation</subject><subject>Cyclophosphamide - administration &amp; dosage</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Hearing Aids</subject><subject>Hearing Loss - chemically induced</subject><subject>Hearing Loss - prevention &amp; 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 &amp; 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 &amp; 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 &amp; dosage</topic><topic>Cranial Irradiation</topic><topic>Cyclophosphamide - administration &amp; dosage</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Hearing Aids</topic><topic>Hearing Loss - chemically induced</topic><topic>Hearing Loss - prevention &amp; 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 &amp; 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 &gt;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>
fulltext fulltext
identifier ISSN: 0732-183X
ispartof Journal of clinical oncology, 2008-08, Vol.26 (22), p.3749-3755
issn 0732-183X
1527-7755
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2504739
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T16%3A44%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Amifostine%20Protects%20Against%20Cisplatin-Induced%20Ototoxicity%20in%20Children%20With%20Average-Risk%20Medulloblastoma&rft.jtitle=Journal%20of%20clinical%20oncology&rft.au=FOULADI,%20Maryam&rft.date=2008-08-01&rft.volume=26&rft.issue=22&rft.spage=3749&rft.epage=3755&rft.pages=3749-3755&rft.issn=0732-183X&rft.eissn=1527-7755&rft_id=info:doi/10.1200/JCO.2007.14.3974&rft_dat=%3Cpubmed_cross%3E18669462%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/18669462&rfr_iscdi=true