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High dose therapy followed by autologous peripheral blood stem cell transplantation as a first line treatment for multiple myeloma: a Korean Multicenter Study.

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dc.contributor.authorBang, SM-
dc.contributor.authorCho, EK-
dc.contributor.authorSuh, C-
dc.contributor.authorYoon, SS-
dc.contributor.authorSeong, CM-
dc.contributor.authorCho, KS-
dc.contributor.authorKang, YG-
dc.contributor.authorPark, S-
dc.contributor.authorAhn, MJ-
dc.contributor.authorPark, YS-
dc.contributor.authorOh, D-
dc.contributor.authorKim, HC-
dc.contributor.authorJung, CW-
dc.contributor.authorKim, S-
dc.contributor.authorLee, JH-
dc.date.accessioned2011-07-15T02:18:20Z-
dc.date.available2011-07-15T02:18:20Z-
dc.date.issued2003-
dc.identifier.issn1011-8934-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/3371-
dc.description.abstractWe conducted a phase II multicenter trial to estimate the response and survival of patients with newly diagnosed multiple myeloma to high dose melphalan therapy followed by autologous peripheral blood stem cell transplantation. Eligible patients who had undergone induction with vincristine, adriamycin and dexamethasone (VAD) should have adequate cardiac, pulmonary and renal function (creatinine <2 mg/dL). Melphalan at 200 mg/m2 was used as a conditioning regimen. Eighty patients were enrolled from 13 centers. The median age of the patients was 53 yr (range; 20 to 68 yr). The initial stage was IA/IIA/IIB/IIIA/IIIB in 3/8/1/54/14 patients, respectively. Beta2-microglobulin, CRP and LDH were increased in 74, 42 and 34% of the patients examined. Cytogenetic data were available in 30 patients, and 6 patients showed numeric or structural abnormalities. Two therapy-related mortalities occurred from infection. Among the 78 evaluable patients, CR/PR/MR/NC/PD were achieved in 48/26/2/1/1 patients, respectively. After a median follow-up of 30 months, the median overall and event-free survivals were 66 months (95% CI: 20-112) and 24 months (95% CI: 18-29), respectively. This study verifies the efficacy and feasibility of high dose melphalan therapy with autologous stem cell transplantation in newly diagnosed multiple myeloma.-
dc.language.isoen-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAntigens, CD34-
dc.subject.MESHAntineoplastic Agents, Alkylating-
dc.subject.MESHC-Reactive Protein-
dc.subject.MESHCell Survival-
dc.subject.MESHCombined Modality Therapy-
dc.subject.MESHCytogenetics-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHKorea-
dc.subject.MESHL-Lactate Dehydrogenase-
dc.subject.MESHMale-
dc.subject.MESHMelphalan-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMultiple Myeloma-
dc.subject.MESHPeripheral Blood Stem Cell Transplantation-
dc.subject.MESHTime Factors-
dc.subject.MESHTransplantation, Autologous-
dc.subject.MESHbeta 2-Microglobulin-
dc.titleHigh dose therapy followed by autologous peripheral blood stem cell transplantation as a first line treatment for multiple myeloma: a Korean Multicenter Study.-
dc.typeArticle-
dc.identifier.pmid14555819-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3055099/-
dc.contributor.affiliatedAuthor김, 효철-
dc.type.localJournal Papers-
dc.identifier.doi10.3346/jkms.2003.18.5.673-
dc.citation.titleJournal of Korean medical science-
dc.citation.volume18-
dc.citation.number5-
dc.citation.date2003-
dc.citation.startPage673-
dc.citation.endPage678-
dc.identifier.bibliographicCitationJournal of Korean medical science, 18(5). : 673-678, 2003-
dc.identifier.eissn1598-6357-
dc.relation.journalidJ010118934-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Hematology-Oncology
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