Source:http://linkedlifedata.com/resource/pubmed/id/15621781
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2004-12-28
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pubmed:abstractText |
The feasibility of intensified therapy in adults < 61-years-old with de novo acute myeloid leukemia (AML) was evaluated by adding high-dose cytarabine (HDAC) to conventional induction therapy and in post-remission therapy prior to peripheral blood stem cell transplantation (PBSCT). Patients were treated with conventional induction therapy (daunorubicin days 1-3 and cytarabine days 1-7), followed by HDAC (2 gm/M2) every 12 h ( x 6) on days 8-10. Patients in complete remission (CR) with HLA-matched siblings were assigned to allogeneic PBSCT; the others received two courses of HDAC (3 gm/M2 every 12 h on days 1, 3, and 5) given 1 month apart. Peripheral blood stem cells were then harvested and infused after high-dose chemotherapy. Of 62 eligible, evaluable patients, 47 (76%) achieved CR. The mortality rate was 10% (6 patients); no deaths occurred during the two post-remission courses of HDAC. Fifteen patients were assigned to allogeneic PBSCT and 32 to autologous PBSCT. All surviving patients have been followed for more than 4 years. Including all patients scheduled to receive autoPBSCT in an intent-to-treat analysis, after a median 5-year follow-up the current, non-actuarial, four-year event-free and overall survival was 47% and 47%, respectively. Intensified induction therapy was associated with more toxicity than conventional induction therapy, and the CR rate did not improve. Nevertheless, intensive post-remission therapy was well tolerated, no treatment-related mortality occurred with autologous PBSCT, and disease-free survival and overall survival were lengthy.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/CA07190,
http://linkedlifedata.com/resource/pubmed/grant/CA11083,
http://linkedlifedata.com/resource/pubmed/grant/CA13650,
http://linkedlifedata.com/resource/pubmed/grant/CA15488,
http://linkedlifedata.com/resource/pubmed/grant/CA17145,
http://linkedlifedata.com/resource/pubmed/grant/CA21115,
http://linkedlifedata.com/resource/pubmed/grant/CA23318,
http://linkedlifedata.com/resource/pubmed/grant/CA66636
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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 |
Jan
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pubmed:issn |
1042-8194
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pubmed:author |
pubmed-author:BennettJohn MJM,
pubmed-author:CassilethPeter APA,
pubmed-author:DewaldGordon WGW,
pubmed-author:Eastern Cooperative Oncology Group,
pubmed-author:LazarusHillard MHM,
pubmed-author:LeeSandra JSJ,
pubmed-author:LitzowMark RMR,
pubmed-author:MillerKenneth BKB,
pubmed-author:PaiettaElisabethE,
pubmed-author:RoweJacob MJM,
pubmed-author:StadtmauerEdward AEA,
pubmed-author:TallmanMartin SMS
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pubmed:issnType |
Print
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pubmed:volume |
46
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
55-61
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:15621781-Adolescent,
pubmed-meshheading:15621781-Adult,
pubmed-meshheading:15621781-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:15621781-Cytarabine,
pubmed-meshheading:15621781-Daunorubicin,
pubmed-meshheading:15621781-Female,
pubmed-meshheading:15621781-Humans,
pubmed-meshheading:15621781-Leukemia, Myeloid, Acute,
pubmed-meshheading:15621781-Male,
pubmed-meshheading:15621781-Middle Aged,
pubmed-meshheading:15621781-Peripheral Blood Stem Cell Transplantation,
pubmed-meshheading:15621781-Remission Induction,
pubmed-meshheading:15621781-Survival Rate,
pubmed-meshheading:15621781-Transplantation, Autologous,
pubmed-meshheading:15621781-Treatment Outcome
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pubmed:year |
2005
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pubmed:articleTitle |
Intensified induction chemotherapy in adult acute myeloid leukemia followed by high-dose chemotherapy and autologous peripheral blood stem cell transplantation: an Eastern Cooperative Oncology Group trial (E4995).
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pubmed:affiliation |
University of Miami/Sylvester Comprehensive Cancer Center, Miami, FL 33136, USA. pcassile@med.miami.edu
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
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