Erythropoietin (Epo) and Venofer Trial After Autologous Hematopoietic Stem Cell Transplantation (HSCT)

Hematological Malignancies Clinical Trial

Official title: Darbepoetin-alpha and i.v. Iron Administration After Autologous Hematopoietic Stem Cell Transplantation : a Prospective Randomized Trial

Status Completed

Clinical Trial Summary

Darbepoetin-alpha and i.v. iron administration after autologous hematopoietic stem cell transplantation for hematological malignancies : a prospective randomized trial.

Clinical Trial Description

1. Outline:

A 3-arm prospective randomized study of darbepoetin alpha administration after autologous PBSC transplantation. Patients in the first arm will receive neither darbepoetin alpha nor i.v. iron. Patients in the second arm will receive darbepoetin alpha (Aranesp) alone starting on day 28 after the transplant. Patients in the third arm will receive darbepoetin alpha (Aranesp) and i.v. iron saccharate (Venofer). The plan is to include 25 patients in each arm.

In September 2006, all 75 planned patients have been included. Whereas preliminary analysis shows that Aranesp therapy significantly improves Hb recovery after autologous PBSC transplantation, the additional impact of Venofer therapy remains statistically not significant. However, this is a very important point, because Venofer therapy could potentially improve response and decrease the overall cost of treatment. Therefore, to increase the statistical power of the study, 50 additional patients will be included. Randomisation will now become limited to arms 2 (Aranesp) and 3 (Aranesp + Venofer).

2. Randomization:

Patients will be randomized 1:1:1 between the "Control", "Aranesp alone" and "Aranesp + Venofer" arms. Randomization will be carried out following a computer-generated randomization list blinded for personnel involved in clinical care of the patients.

Randomization will be carried out centrally in Liège by faxing the inclusion form at the following number : 32-4-3668855. This should be done around day 21 post-transplant.

Starting in September 2006, patients will be randomized 1:1 between the "Aranesp alone" and "Aranesp + Venofer" arms, using a computer-generated randomization list.

3. Study drug administration:

• Darbepoetin alpha administration : Darbepoetin alpha (Aranesp) will be administered s.c. at the dose of 300 µg. The first dose will be given on day 28 and the following doses at 2-wk intervals around days 42, 56, 70, 84, 98, and 112 post-transplant. Once the target Hb (13 g/dL) has been attained, the dose of Aranesp will be reduced by half to 150 µg. If the Hb increases to > 14 g/dL, Aranesp will be withheld and resumed at the dose of 150 µg when the Hb decreases < 13 g/dL. If the Hb decreases to < 12 g/dL, the dose of Aranesp will be increased to 300 µg again.

• Iron administration: Iron saccharate (Venofer) will be administered i.v. at the dose of 200 mg (2 vials of Venofer) on days 28, 42, and 56 after the transplant. Venofer will be diluted in 250 ml saline and infused over 60 minutes. Iron will be omitted in patients with severe iron overload (serum ferritin > 2500 µg/L in the absence of inflammation or liver necrosis) or elevated transferrin saturation (TS > 60%) between days 21 and 56. No iron supplementation will be allowed in arm 1. No iron supplementation will be allowed in arm 2 before day 70 after the transplant. In arms 2 and 3, if patients have evidence of functional iron deficiency (Transferrin saturation < 20%) on day 70 or later, they may receive 300 mg of Venofer over 90 min, for a minimum of 2 doses.

4. Transfusions:

One red blood cell (RBC) unit will be transfused if Hb value is between 7.0 and 7.9 g/dL. Two RBC units will be transfused if Hb value is below 7 g/dL. Platelets will be transfused if needed, as per the institution's standards.

5. Follow-up:

• Clinical follow-up : Potential toxicities associated with Aranesp or Venofer will be carefully monitored per the institution's standards. Blood pressure will be recorded around days 28, 42, 56, 70, 84, 98, 112, and 126 after the transplant. Serious adverse events (such as infections, bleeding, disease progression, any hospitalization) will be recorded. In case of serious adverse event judged as potentially related to Aranesp or Venofer, the principal investigator will be immediately notified so as to jointly decide on possible discontinuation of either drug.

Quality-of-life (QOL) evaluations will be carried out at baseline (day 28) as well as on days 70 and 126 after the transplant, i.e. after 3 and 7 doses of Aranesp therapy. This will be accomplished by providing the patient will the validated FACT-anemia questionnaire. The questionnaire will be filled out by the patient and returned to the principal investigator.

• Laboratory analyses: Complete blood counts will be determined in an automated cell counter. Percentage and absolute reticulocyte count will be obtained locally by an automated cytofluorometric method. Serum erythropoietin (Epo) levels will be measured centrally in Liège on stored samples by a commercially available radioimmunoassay (Incstar Corp., Stillwater, MN, USA). Based on regression equations obtained in appropriate reference subjects between Hct on the one hand and log (Epo) on the other, predicted log (Epo) values are derived for each Hct and O/P ratios of observed/predicted Epo values will be calculated. Serum soluble transferrin receptor (sTfR), a quantitative measure of total erythropoietic activity, will be measured centrally in Liège on stored samples by a commercially available ELISA (R&D, Minneapolis, MN, USA). Normal values range from 3,000 to 7,000 µg/L. Serum iron, transferrin saturation and ferritin, as well as standard biochemical values, will be measured locally by standard methods.

On days 28 and 42, 5 ml of blood without anticoagulant will be collected and centrifuged within 2 hours, serum will be separated and 2 ml of serum will be stored at -28°C. Stored samples will be collected by the local investigator and finally stored in Liège. Serum Epo and soluble TfR will be assayed later on all samples simultaneously.

6. Data collection and analysis:

Data will be collected at each center on protocol forms. The coordinating data manager from Liège will verify the completeness and accuracy of data collected. The coordinating data manager will be responsible for entering these data into the central database. All statistical analyses will be performed centrally in Liège. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Hematological Malignancies

• NCT number: NCT00557817
• Study type: Interventional
• Source: University Hospital of Liege
• Status: Completed
• Phase: Phase 2/Phase 3
• Start date: March 2004
• Completion date: August 2008