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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
1992-10-29
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pubmed:abstractText |
To improve the safety of autotransplantation for myeloma, peripheral blood stem cell (PBSC) collection was attempted in 75 previously treated patients after the administration of high-dose cyclophosphamide (HD-CTX; 6 g/m2) with or without granulocyte-macrophage colony-stimulating factor (GM-CSF). Sixty patients subsequently received melphalan 200 mg/m2 (57 patients) or melphalan 140 mg/m2 and total body irradiation (850 cGy) (3 patients) supported by both autologous bone marrow and PBSC; 38 patients received GM-CSF posttransplantation. Among 72 patients undergoing PBSC apheresis, "good" mobilization (greater than 50 colony-forming units granulocyte-macrophage [CFU-GM] per 10(5) mononuclear cells) was achieved when prior chemotherapy did not exceed 1 year and when GM-CSF was used post-HD-CTX; similarly, rapid platelet recovery to 50,000/microL within 2 weeks was associated with "good" PBSC mobilization. These same variables also predicted for rapid engraftment after autotransplantation, so that hematologic recovery (granulocytes greater than 500/microL and platelets greater than 50,000/microL) proceeded within 2 weeks among the 37 patients with "good" PBSC collection. As a result of rapid neutrophil recovery (greater than 500/microL) within a median of 2 weeks, infectious complications both post-HD-CTX and posttransplant were readily manageable, resulting in only one treatment-related death post-HD-CTX. The cumulative response rate (greater than or equal to 75% cytoreduction) for all 75 patients was 68%, with 12-month event-free and overall survival projections of about 85%. Using both bone marrow and PBSC together with GM-CSF, autotransplants are safe and appear effective in myeloma, especially when prior therapy had been limited to less than 1 year. More than 80% of transplanted patients achieved complete hematologic recovery within a median of 1 month posttransplant (granulocytes greater than 1,500/microL; platelets greater than 100,000/microL; hemoglobin greater than 10 g%), thus providing sufficient hematopoietic reserve for further chemotherapy in the event of posttransplant relapse.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0006-4971
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
80
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1666-72
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1391937-Bone Marrow Transplantation,
pubmed-meshheading:1391937-Colony-Forming Units Assay,
pubmed-meshheading:1391937-Combined Modality Therapy,
pubmed-meshheading:1391937-Cyclophosphamide,
pubmed-meshheading:1391937-Follow-Up Studies,
pubmed-meshheading:1391937-Granulocyte-Macrophage Colony-Stimulating Factor,
pubmed-meshheading:1391937-Humans,
pubmed-meshheading:1391937-Melphalan,
pubmed-meshheading:1391937-Middle Aged,
pubmed-meshheading:1391937-Multiple Myeloma,
pubmed-meshheading:1391937-Stem Cell Transplantation,
pubmed-meshheading:1391937-Survival Analysis,
pubmed-meshheading:1391937-Transplantation, Autologous,
pubmed-meshheading:1391937-Whole-Body Irradiation
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pubmed:year |
1992
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pubmed:articleTitle |
Low-risk intensive therapy for multiple myeloma with combined autologous bone marrow and blood stem cell support.
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pubmed:affiliation |
Division of Hematology/Oncology, University of Arkansas for Medical Sciences, Little Rock 72205.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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