Korean J Hematol 2010; 45(2):
Published online June 30, 2010
https://doi.org/10.5045/kjh.2010.45.2.95
© The Korean Society of Hematology
1Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
2Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
3Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
4Department of Preventive Medicine, University of Ulsan College of Medicine, Seoul, Korea.
Correspondence to : Correspondence to Sung-Soo Yoon, M.D. Department of Internal Medicine, Seoul National University College of Medicine, Clinical Research Institute, Seoul National University Hospital, 28, Yeongeon-dong, Jongno-gu, Seoul 110-744, Korea. Tel: +82-2-2072-3079, Fax: +82-2-762-9662, ssysmc@snu.ac.kr
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
The role of pre-transplant salvage chemotherapy has been controversial in relapsed acute leukemia.
We investigated post-transplant outcomes in 65 patients with acute leukemia treated with allogeneic hematopoietic cell transplantation (HCT) during first relapse or second remission.
The 5-year cumulative incidence of relapse (CIR) was 52.3%. Multivariate analysis for CIR revealed that patients with unfavorable cytogenetics and those not in remission at the time of HCT had a significantly high CIR (
Our results do not support the role of salvage chemotherapy aimed at re-induction of remission before allogeneic HCT in patients with acute leukemia after first relapse. Patients with early relapse do not appear to benefit from salvage chemotherapy before HCT.
Keywords Allogeneic HCT, Acute leukemia, First relapse, Second remission
Korean J Hematol 2010; 45(2): 95-101
Published online June 30, 2010 https://doi.org/10.5045/kjh.2010.45.2.95
Copyright © The Korean Society of Hematology.
Je-Hwan Lee1, Sung-Soo Yoon2*, Chul Won Jung3, Jung-Hee Lee1, Dae-Young Kim1, Young-Shin Lee1, Sung Cheol Yun4, Inho Kim2, Seonyang Park2, Byoung Kook Kim2, Kihyun Kim3, Jin Seok Ahn3, and Kyoo-Hyung Lee1
1Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
2Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
3Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
4Department of Preventive Medicine, University of Ulsan College of Medicine, Seoul, Korea.
Correspondence to: Correspondence to Sung-Soo Yoon, M.D. Department of Internal Medicine, Seoul National University College of Medicine, Clinical Research Institute, Seoul National University Hospital, 28, Yeongeon-dong, Jongno-gu, Seoul 110-744, Korea. Tel: +82-2-2072-3079, Fax: +82-2-762-9662, ssysmc@snu.ac.kr
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
The role of pre-transplant salvage chemotherapy has been controversial in relapsed acute leukemia.
We investigated post-transplant outcomes in 65 patients with acute leukemia treated with allogeneic hematopoietic cell transplantation (HCT) during first relapse or second remission.
The 5-year cumulative incidence of relapse (CIR) was 52.3%. Multivariate analysis for CIR revealed that patients with unfavorable cytogenetics and those not in remission at the time of HCT had a significantly high CIR (
Our results do not support the role of salvage chemotherapy aimed at re-induction of remission before allogeneic HCT in patients with acute leukemia after first relapse. Patients with early relapse do not appear to benefit from salvage chemotherapy before HCT.
Keywords: Allogeneic HCT, Acute leukemia, First relapse, Second remission
Overall survival and event-free survival curves.
Cumulative incidences of relapse and non-relapse mortality.
Cumulative incidence of relapse relative to salvage chemotherapy aimed at reinduction of complete remission (CR) before hematopoietic cell transplantation: second CR vs. untreated relapse vs. refractory relapse.
Cumulative incidence of relapse relative to bone marrow blast percentage before hematopoietic cell transplantation.
Table 1 . Patient and transplantation characteristics..
Abbreviations: M, male; F, female; AML, acute myeloid leukemia; ALL, acute lymphoblastic leukemia; BAL, biphenotypic acute leukemia; HCT, hematopoietic cell transplantation; CR, complete remission; BuCy, busulfan-cyclophosphamide; TBI, total body irradiation; RIC, reduced-intensity conditioning; CSA, cyclosporine; MTX, methotrexate; CS, corticosteroid; BM, bone marrow; PB, peripheral blood; CB, cord blood..
Table 2 . Multivariate analysis of prognostic factors for survival probabilities and cumulative incidences..
Abbreviations: a)Cox proportional hazards regression model; b)Gray's method..
MTX, methotrexate; HCT, hematopoietic cell transplantation; CR2, second complete remission; GVHD, graft-versus-host disease..
Table 3 . Clinical outcomes after allogeneic hematopoietic cell transplantation according to disease status..
Abbreviation: CR: complete remission..
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Overall survival and event-free survival curves.
|@|~(^,^)~|@|Cumulative incidences of relapse and non-relapse mortality.
|@|~(^,^)~|@|Cumulative incidence of relapse relative to salvage chemotherapy aimed at reinduction of complete remission (CR) before hematopoietic cell transplantation: second CR vs. untreated relapse vs. refractory relapse.
|@|~(^,^)~|@|Cumulative incidence of relapse relative to bone marrow blast percentage before hematopoietic cell transplantation.