2016
DOI: 10.3324/haematol.2016.153130
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Low-dose clofarabine in combination with a standard remission induction in patients aged 18–60 years with previously untreated intermediate and bad-risk acute myeloid leukemia or high-risk myelodysplastic syndrome: combined phase I/II results of the EORTC/GIMEMA AML-14A trial

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Cited by 5 publications
(3 citation statements)
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“…Secondary acute myeloid leukaemia (AML) has been classified as AML occurring after prior myeloid disease including myelodysplastic syndrome (MDS) or myeloproliferative neoplasm (MPN) while therapy-related AML (tAML) has been defined as AML occurring after exposure to radiation or chemotherapy [1,2]. Many prior studies have grouped these two categories as 'secondary AML (sAML)' [3][4][5][6]. In most reports, sAML represents approximately 25% of all AML patients [7,8].…”
Section: Introductionmentioning
confidence: 99%
“…Secondary acute myeloid leukaemia (AML) has been classified as AML occurring after prior myeloid disease including myelodysplastic syndrome (MDS) or myeloproliferative neoplasm (MPN) while therapy-related AML (tAML) has been defined as AML occurring after exposure to radiation or chemotherapy [1,2]. Many prior studies have grouped these two categories as 'secondary AML (sAML)' [3][4][5][6]. In most reports, sAML represents approximately 25% of all AML patients [7,8].…”
Section: Introductionmentioning
confidence: 99%
“…Although the overall survival (OS) in younger acute myeloid leukemia (AML) patients has improved in the recent decades, disease relapse remains the first cause of death in younger patients with AML [1][2][3][4][5][6]. Approximately 60% of younger patients diagnosed with AML have chromosomal aberrations in their leukemic cells [1].…”
Section: Introductionmentioning
confidence: 99%
“…Nevertheless, high-dose conditioning regimen administered before myeloablative allo-HCT as well as intensive chemotherapy regimens used to treat AML still results in prolonged bone marrow aplasia and particularly prolonged neutropenia that often leads to bacterial and/or fungal infections [3][4][5][6]. This is particularly the case when umbilical cord blood (UCB) is chosen as stem cell source for allo-HCT [4], or when the intensity of the chemotherapy is increased in the induction or consolidation chemotherapy course of AML [7].…”
Section: Introductionmentioning
confidence: 99%