Source:http://linkedlifedata.com/resource/pubmed/id/11372740
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2001-5-24
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pubmed:abstractText |
The antitumor effect of high-dose chemotherapy (HDC) followed by autologous peripheral blood stem cell transplantation (auto-PBSCT) is considered superior to that of conventional chemotherapy. However, the long-term benefits of this strategy in Japan remain unclear. Therefore, in this study, 109 cancer patients enrolled between 1989 and 1999 were treated with HDC and auto-PBSCT. Patients were evaluated for long-term survival and late-onset complications, including secondary malignancy. The mean number of CD34+ cells harvested per apheresis was larger in the group receiving high-dose cytosine arabinoside or high-dose etoposide plus granulocyte colony-stimulating factor (G-CSF) than in the group receiving conventional chemotherapy plus G-CSF. The 5-year overall survival rates for non-Hodgkin's lymphoma patients in first complete remission (CR) (83.2%), second or subsequent CR (74.1%), or first partial remission (PR) (66.7%) at the time of transplantation were significantly higher than those with no remission (35.7%) at the time of transplantation (first CR, P < .05; second or subsequent CR, P < .05; first PR, P < .05). The 5-year overall survival (OS) rates for breast cancer was 40.8%, and the disease-free survival rate was extremely low (8.8%). The 5-year OS rates for chemotherapy-sensitive and chemotherapy-resistant diseases at the time of transplantation were 32.7% and 35.7%, respectively, a difference that was not considered significant. The 5-year OS for germ cell tumor was 80.0%, and the disease-free survival rate was 77.9%. The rate of therapy-related death was 8.2%. The occurrence rate of secondary malignancy was 0.9%. Late-onset complications were observed in 4 cases (glomerulonephritis, interstitial pneumonitis, ulcerative colitis, and acute myelogenous leukemia). At 3.7%, the occurrence rate was not very high, but most complications of auto-PBSCT were life threatening and interfered with patients' quality of life. A careful follow-up is required for at least 2 years after transplantation, because the mean occurrence time of late-onset complications is 16.7 months posttransplantation.
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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 |
Feb
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pubmed:issn |
0925-5710
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pubmed:author |
pubmed-author:AkiyamaTT,
pubmed-author:FujimeMM,
pubmed-author:HirataYY,
pubmed-author:HirayamaYY,
pubmed-author:Hokkaido Society of Peripheral Blood Stem Cell Transplantation,
pubmed-author:KogawaKK,
pubmed-author:KohdaKK,
pubmed-author:KoikeKK,
pubmed-author:KonumaYY,
pubmed-author:KugaTT,
pubmed-author:KusakabeTT,
pubmed-author:MatsunagaTT,
pubmed-author:NiitsuG YGY,
pubmed-author:NishisatoTT,
pubmed-author:NojiriSS,
pubmed-author:SakamakiSS,
pubmed-author:SasagawaYY
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pubmed:issnType |
Print
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pubmed:volume |
73
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
251-7
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pubmed:dateRevised |
2006-4-24
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pubmed:meshHeading |
pubmed-meshheading:11372740-Adult,
pubmed-meshheading:11372740-Antigens, CD34,
pubmed-meshheading:11372740-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:11372740-Blood Component Removal,
pubmed-meshheading:11372740-Female,
pubmed-meshheading:11372740-Follow-Up Studies,
pubmed-meshheading:11372740-Hematopoietic Stem Cell Transplantation,
pubmed-meshheading:11372740-Humans,
pubmed-meshheading:11372740-Male,
pubmed-meshheading:11372740-Middle Aged,
pubmed-meshheading:11372740-Neoplasms,
pubmed-meshheading:11372740-Neoplasms, Second Primary,
pubmed-meshheading:11372740-Survival Rate,
pubmed-meshheading:11372740-Transplantation, Autologous,
pubmed-meshheading:11372740-Treatment Outcome
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pubmed:year |
2001
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pubmed:articleTitle |
Long-term survival and late-onset complications of cancer patients treated with high-dose chemotherapy followed by autologous peripheral blood stem cell transplantation.
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pubmed:affiliation |
Japanese Red Cross Asahikawa Hospital, Sapporo Medical University School of Medicine, Japan.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Multicenter Study
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