Format

Send to

Choose Destination
J Cancer Res Clin Oncol. 2018 May 14. doi: 10.1007/s00432-018-2665-x. [Epub ahead of print]

Tolerability and efficacy of deferasirox in patients with transfusional iron overload: results from a German 2-year non-interventional study.

Author information

1
Department of Hematology and Oncology, University Hospital Mannheim, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Germany. florian.nolte@medma.uni-heidelberg.de.
2
Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany. florian.nolte@medma.uni-heidelberg.de.
3
Medical Practice for Hematology, Oncology, Hemostaseology and Palliative Care, Bochum, Germany.
4
Medical Practice for Hematology and Oncology, Munich, Germany.
5
Department for Internal Medicine III, Hematology, Oncology and Palliative Care, Diakonie-Klinikum, Schwäbisch Hall, Germany.
6
Medical Practice for Hematology and Oncology, Hamelin, Germany.
7
Center for Internal Medicine, Stauferklinikum Schwäbisch Gmünd, Mutlangen, Germany.
8
Division for Stem Cell Transplantation and Immunology, Department for Children and Adolescents, University Hospital, Goethe University Frankfurt am Main, Frankfurt, Germany.
9
Novartis Pharma GmbH, Nuremberg, Germany.
10
Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
11
Department of Hematology and Oncology, University Hospital Mannheim, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Germany.

Abstract

BACKGROUND:

Iron overload (IOL) due to repetitive transfusions of packed red blood cells (pRBC) has a major impact on morbidity and mortality in patients with inherited bone marrow failure syndromes and hemoglobinopathies such as thalassemia and sickle cell disease. However, whether IOL influences the outcome of elderly patients with myeloid malignancies is not yet clear. Moreover, clinical trials have reported high drop-out rates during treatment with the oral iron chelator deferasirox (DFX).

AIM:

Here we report the results of a 2-year prospective observational study that aimed at describing the routine use of DFX in patients with hematological malignancies with regard to safety, efficacy and handling of the drug in a routine setting.

RESULTS:

A total of 406 patients were included. 58% of the patients were male. Most of the patients had myelodysplastic syndromes (MDS) (68%) and myeloproliferative neoplasms (MPN) (14%). Median time from first transfusion to study enrollment was 1.1 years (0-25.5 years) and most patients were chelation naive (91%) at enrollment. With regard to transfusion burden, most of the patients were moderately or mildly transfusion-dependent with 53% receiving 2-4 and 27% receiving less than 2 units of pRBC per month. Serum ferritin decreased from a mean of 2305 μg/l (± 1449 μg/l) to a mean of 1910 μg/l (± 1529 μg/l) at 24 months. There was no substantial change in transfusion-dependence during the observation period. Dose adjustments were reported in 48% of the patients with dose-escalation strategies being the most frequent reason for dosage increases (49%). The median observation time was 355 days (5-1080 days). Median duration of exposure to DFX was 322 days (2-1078 days). Two-hundred and ninety (72%) patients discontinued the trial prematurely after a median time of 235 days (1-808 days). Death (29%) and adverse events (23%) were the main reasons for discontinuation. Eleven percent of the patients discontinued treatment due to sufficient decrease in serum ferritin. Most frequent adverse events were decrease in creatinine clearance (22%), increase in serum creatinine (18%) and diarrhea (16%).

CONCLUSION:

This descriptive trial confirms the efficacy of DFX in decreasing the serum ferritin. Moreover, the high drop-out rates seen in prospective trials are recapitulated in this study, which can be attributed to adverse events in a substantial proportion of patients.

KEYWORDS:

Adverse event; Deferasirox; Hematologic disease; Iron overload; Myelodysplastic syndrome; Transfusion

PMID:
29761371
DOI:
10.1007/s00432-018-2665-x

Supplemental Content

Full text links

Icon for Springer
Loading ...
Support Center