2016
DOI: 10.1016/j.leukres.2016.04.014
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Idarubicin-intensified BUCY2 conditioning regimen improved survival in high-risk acute myeloid, but not lymphocytic leukemia patients undergoing allogeneic hematopoietic stem cell transplantation: A retrospective comparative study

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Cited by 12 publications
(11 citation statements)
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“…A cohort of 98 consecutive patients with high-risk acute leukemia who underwent their first allo-HSCT using IDA-intensified conditioning regimens from January 2012 to January 2017 at the Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, were included in this retrospective study. We classified patients as high risk at diagnosis following the criteria in our previous reports [9][10][11][12]. The definition of high-risk AML were no response to induction chemotherapy, relapse within 6 months after induction or consolidation therapy, relapse within 6 months after induction therapy that could not be relieved using the original induction therapy, 2 relapses or relapse after auto-HSCT, unfavorable cytogenetics, or a history of preceding neoplasia and/or chemotherapy in no remission (NR).…”
Section: Eligibility Criteriamentioning
confidence: 99%
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“…A cohort of 98 consecutive patients with high-risk acute leukemia who underwent their first allo-HSCT using IDA-intensified conditioning regimens from January 2012 to January 2017 at the Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, were included in this retrospective study. We classified patients as high risk at diagnosis following the criteria in our previous reports [9][10][11][12]. The definition of high-risk AML were no response to induction chemotherapy, relapse within 6 months after induction or consolidation therapy, relapse within 6 months after induction therapy that could not be relieved using the original induction therapy, 2 relapses or relapse after auto-HSCT, unfavorable cytogenetics, or a history of preceding neoplasia and/or chemotherapy in no remission (NR).…”
Section: Eligibility Criteriamentioning
confidence: 99%
“…The definition of hematopoietic engraftment was similar to that reported previously [9][10][11][12]. Chimerism was typically evaluated in recipient BM or whole peripheral blood without separation usually on days +30, +90, +180, +270, and +360 after transplantation.…”
Section: Hematopoietic Engraftment and Transplant-related Toxicitymentioning
confidence: 99%
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“…A high incidence of severe oral toxicity is observed i n pat ient s w it h mu lt iple myelom a (MM), non-Hodgkin's lymphoma (NHL), and acute myeloid leukemia (AML) who have received highdose melphalan, BEAM (carmustine, etoposide, cytarabine, and melphalan), and BuCy (busulfan plus cyclophosphamide) conditioning regimens, respectively, and autologous or allogeneic HSCT. 11,12 A preventive protocol using photobiomodulation (PBM) is currently considered to be an important tool for the reduction of the incidence and severity of OM in patients receiving high doses of chemotherapy and/ or radiotherapy before HSCT. 13,14 Also, some studies have demonstrated an economic value of PBM based on the fact that this tool reduces costs that result in savings of US$5,000 per prevented OM case.…”
Section: Introductionmentioning
confidence: 99%