Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2005-5-2
pubmed:abstractText
Following a dose-escalation study performed to assess the maximally tolerated dose of high-dose mitoxantrone in a single injection combined with chemotherapy, a phase II trial (EMA 2000 regimen) was performed in patients with refractory or relapsed acute myelogenous leukemia (AML) between October 2000 and December 2003. Sixty-two patients entered the study and received mitoxantrone 45 mg/m(2) on day 1 in combination with cytarabine and etoposide. Overall, 39 patients (63%) achieved complete remission (CR). Four patients died during remission induction, and 19 patients had resistant disease. Median time to granulocyte and platelet recovery was 34 and 39 days, respectively. The predominant non-hematologic toxicity was infection, with 53% severe infections. Thirty-three of the 39 remitters received subsequent treatment consisting of maintenance chemotherapy courses in 17 patients, allogeneic stem cell transplantation (SCT) in 7 patients, and autologous SCT in 9 patients. The median overall survival of the entire cohort was 8.1 months, with 18% at 2.5 years. EMA chemotherapy using a single injection of mitoxantrone is effective in the treatment of high-risk AML. CR proportion was significantly higher in patients with a first CR duration > or =6 months when compared with those from a control trial using standard-dose mitoxantrone (90 vs 70%, p=0.03).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0939-5555
pubmed:author
pubmed:issnType
Print
pubmed:volume
84
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
376-82
pubmed:meshHeading
pubmed-meshheading:15782343-Acute Disease, pubmed-meshheading:15782343-Adolescent, pubmed-meshheading:15782343-Adult, pubmed-meshheading:15782343-Aged, pubmed-meshheading:15782343-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:15782343-Bone Marrow Transplantation, pubmed-meshheading:15782343-Combined Modality Therapy, pubmed-meshheading:15782343-Dose-Response Relationship, Drug, pubmed-meshheading:15782343-Drug Administration Schedule, pubmed-meshheading:15782343-Female, pubmed-meshheading:15782343-Follow-Up Studies, pubmed-meshheading:15782343-Gastrointestinal Diseases, pubmed-meshheading:15782343-Hematologic Diseases, pubmed-meshheading:15782343-Humans, pubmed-meshheading:15782343-Infection, pubmed-meshheading:15782343-Infusions, Intravenous, pubmed-meshheading:15782343-Leukemia, Myeloid, pubmed-meshheading:15782343-Life Tables, pubmed-meshheading:15782343-Male, pubmed-meshheading:15782343-Middle Aged, pubmed-meshheading:15782343-Mitoxantrone, pubmed-meshheading:15782343-Prognosis, pubmed-meshheading:15782343-Remission Induction, pubmed-meshheading:15782343-Risk, pubmed-meshheading:15782343-Stomatitis, pubmed-meshheading:15782343-Survival Analysis, pubmed-meshheading:15782343-Treatment Outcome
pubmed:year
2005
pubmed:articleTitle
Intensive chemotherapy with mitoxantrone administered as a single injection in patients with high-risk acute myeloid leukemia: results of the EMA 2000 trial.
pubmed:affiliation
Service d'Hématologie, Hôpital Edouard Herriot, 69437, Lyon cedex 03, France. xavier.thomas@chu-lyon.fr
pubmed:publicationType
Journal Article, Clinical Trial, Multicenter Study, Clinical Trial, Phase II