Combination of clofarabine, cyclophosphamide, and etoposide for relapsed or refractory childhood and adolescent acute myeloid leukemia.
Yoav H MessingerJessica BoklanJohn GoldbergSteven G DuBoisJavier OesterheldOussama AblaAlissa MartinJoanna WeinsteinNobuko HijiyaPublished in: Pediatric hematology and oncology (2017)
Relapsed/refractory acute myeloid leukemia (AML) has an extremely poor prognosis. We describe 17 children and adolescents with relapsed/refractory AML who received clofarabine, cyclophosphamide, and etoposide. Seven patients (41%) responded: 4 with a complete response (CR); 1 with CR with incomplete platelet recovery; and 2 with a partial response. Additionally, 4 developed hypocellular marrow without evidence of leukemia; 5 patients had resistant disease; and 1 suffered early toxic death. After further therapy including transplantation, 4 patients (24%) are alive without evidence of disease at a median of 60 months. This anthracycline-free regimen may be studied for relapsed or refractory AML, but due to the high risk of marrow aplasia reduced doses of clofarabine and cyclophosphamide should be used.
Keyphrases
- acute myeloid leukemia
- end stage renal disease
- poor prognosis
- allogeneic hematopoietic stem cell transplantation
- newly diagnosed
- ejection fraction
- chronic kidney disease
- acute lymphoblastic leukemia
- low dose
- prognostic factors
- diffuse large b cell lymphoma
- multiple myeloma
- peritoneal dialysis
- stem cells
- long non coding rna
- patient reported outcomes
- bone marrow
- mesenchymal stem cells
- smoking cessation
- early life
- childhood cancer