Author/Authors :
Zareifar Soheila نويسنده , Abdolkarimi Babak نويسنده Pediatric Hematology-Oncology Division, Department of Pediatrics, Shiraz University of Medical Sciences, Shiraz, Iran , Karimi Mehran نويسنده Hematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran , Salajegheh Pouria نويسنده Department of Pediatric Hematology-Oncology, Iran University of Medical Sciences, Tehran, Iran
Abstract :
Background: Anthracycline therapy for acute leukemia may be associated with
significant morbidity and mortality in children or elderly patients that have a degree
of heart failure. Patients with prior anthracycline exposure, those with pre-existing
heart disease, or who have received the total anthracycline dose present an increased
risk for cardiotoxicity. Therefore, new chemotherapy regimens in these situations would
be life saving for leukemia patients. We have conducted a systematic review of possible
strategies for rescue regimens without anthracycline in refractory acute leukemia
patients.
Methods: We gathered the data from 5 creation databases and relevant website
until August 2016. We selected randomized clinical trials or other studies that used
anthracycline-free chemotherapy regimens to treat acute refractory leukemia in
children and adults. The quality of the studies was evaluated according to the
Cochrane risk of the polarization tool. All stages of the review were independently
conducted by two authors. We obtained data from 75 main clinical trials.
Results: There were 75 trials included from which 4 were considered to be at low
risk for bias. Most trials showed that the improvement did not reach statistical
significance.
Conclusion: Evidence existed to support the use of the combination of fludarabine,
cytarabine, and filgrastim, ICE-rituximab chemotherapy regimens, or monoclonal
antibodies such as tyrosine kinase inhibitors (Sorafenib) useful for acute
refractory/relapsed leukemia.These drugs are used as first salvage regimens or
clofarabine and cladribine for acute myeloid leukemia in patients for whom combined
anthracycline chemotherapy is inappropriate.