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Autologous Peripheral Blood Stem Cell Transplantation Using G-CSF Combined Conditioning in AML Patients  

Kim, Byung Soo (Department of Internal Medicine, Korea University Medical Center)
Kook, Hoon (Department of Pediatrics, Chonnam National University Hospital)
Hwang, Tai Ju (Department of Pediatrics, Chonnam National University Hospital)
Choi, Chul Won (Department of Internal Medicine, Korea University Medical Center)
Kim, Jun Suk (Department of Internal Medicine, Korea University Medical Center)
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IMMUNE NETWORK / v.2, no.1, 2002 , pp. 49-52 More about this Journal
Abstract
Background: The possibility that G-CSF recruits leukemic cells from the G0 to S phase, which may lead to a greater susceptibility to cytotoxic drugs, such as ara-C, has been presented in Harada's study. Methods: In this study, we referred to the protocol of Harada et al 1 to try G-CSF combined marrow-ablative chemotherapy and autologous PBSCT, for the treatment of AML patients in CR1 status. Between January 1997 and March 1998, six AML patients (3: children, 3: adults) in CR1 status were autografted and followed up to 3 years. Results: The major regimen related toxicity was composed of mucositis and diarrhea without death. The time of ANC recovery to 500/L and 1,000/L was 11~48 and 16~81 days, respectively. The mean time of platelet recovery to 20,000/L and 50,000/L was 21~233 and 35~370 days, respectively. The platelet recovery time to 50,000/L was markedly prolonged for more than 100 days in four patients (66.7%). Moreover, four patients (66.7%) experienced a relapse of leukemia after transplantation, with a mean interval of 147.5 days after PBSCT. Two patients were in CR status for 53 and 51 months after PBSCT, respectively. Conclusion: The G-CSF combined marrow-ablative chemotherapy and autologous PBSCT resulted in a markedly delayed platelet recovery and no advantages for decreasing the relapse rate of AML. But, further studies will be warranted.
Keywords
G-CSF combined myeloablative chemotherapy; autologous PBSCT;
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