Source:http://linkedlifedata.com/resource/pubmed/id/19289491
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2009-10-2
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pubmed:abstractText |
This phase I clinical trial conducted with patients who had recurrent or progressive malignant glioma (MG) was designed to determine the maximum tolerated dose (MTD) and toxicity of three different 5-day dosing regimens of temozolomide (TMZ) in combination with O(6)-benzylguanine (O(6)-BG). Both TMZ and O(6)-BG were administered on days 1-5 of a 28-day treatment cycle. A bolus infusion of O(6)-BG was administered at 120 mg/m(2) over 1 h on days 1, 3, and 5, along with a continuous infusion of O(6)-BG at 30 mg/m(2)/day. TMZ was administered at the end of the first bolus infusion of O(6)-BG and then every 24 h for 5 days during the continuous infusion of O(6)-BG. Patients were accrued to one of three 5-day dosing regimens of TMZ. Twenty-nine patients were enrolled into this study. The dose-limiting toxicities (DLTs) were grade 4 neutropenia, leukopenia, and thrombocytopenia. The MTD for TMZ for the three different 5-day dosing schedules was determined as follows: schedule 1, 200 mg/m(2) on day 1 and 50 mg/m(2)/day on days 2-5; schedule 2, 50 mg/m(2)/day on days 1-5; and schedule 3, 50 mg/m(2)/day on days 1-5 while receiving pegfilgrastim. Thus, the 5-day TMZ dosing schedule that maximized the total dose of TMZ when combined with O(6)-BG was schedule 1. This study provides the foundation for a phase II trial of O(6)-BG in combination with a 5-day dosing schedule of TMZ in TMZ-resistant MG.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1522-8517
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pubmed:author |
pubmed-author:BignerDarell DDD,
pubmed-author:DesjardinsAnnickA,
pubmed-author:FriedmanAllan HAH,
pubmed-author:FriedmanHenry SHS,
pubmed-author:GururanganSridharanS,
pubmed-author:HerndonJames EJEJr,
pubmed-author:JiangSara XiaoyinSX,
pubmed-author:McLendonRoger ERE,
pubmed-author:QuinnJennifer AJA,
pubmed-author:ReardonDavid ADA,
pubmed-author:RichJeremy NJN,
pubmed-author:SampsonJohn HJH,
pubmed-author:VredenburghJames JJJ,
pubmed-author:WalkerAmyA
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pubmed:issnType |
Print
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
556-61
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pubmed:dateRevised |
2010-10-4
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pubmed:meshHeading |
pubmed-meshheading:19289491-Adult,
pubmed-meshheading:19289491-Aged,
pubmed-meshheading:19289491-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:19289491-Brain Neoplasms,
pubmed-meshheading:19289491-Dacarbazine,
pubmed-meshheading:19289491-Female,
pubmed-meshheading:19289491-Glioma,
pubmed-meshheading:19289491-Guanine,
pubmed-meshheading:19289491-Humans,
pubmed-meshheading:19289491-Male,
pubmed-meshheading:19289491-Maximum Tolerated Dose,
pubmed-meshheading:19289491-Middle Aged,
pubmed-meshheading:19289491-Neoplasm Recurrence, Local,
pubmed-meshheading:19289491-Treatment Outcome
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pubmed:year |
2009
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pubmed:articleTitle |
Phase I trial of temozolomide plus O6-benzylguanine 5-day regimen with recurrent malignant glioma.
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pubmed:affiliation |
Dept. of Medicine, Division of Neurology, Duke University Medical Center, Durham, NC, USA. quinn008@mc.duke.edu
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pubmed:publicationType |
Journal Article,
Clinical Trial, Phase I,
Research Support, N.I.H., Extramural
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