Treatment of Anemia With Epoetin Beta in Low Risk Myelodysplastic Syndrome (MDS)

• Status: Completed
• Trial end date: 2014-03-01
• Target enrollment: 0
• Participant gender: All

Summary

Chronic anemia is the symptom most frequently found at diagnosis in low risk myelodysplastic syndrome. It generates an increased rate of morbidity and mortality in this population of patients whose median age is high and the rate of co-mobidities important. The historical treatment is limited to transfusion support with a significant impact on quality of life and the incidence of secondary haemosiderosis, which contributes to the emergence of co-morbidities, especially cardiovascular. Treatment with rHuEPO allows for overall erythroid response in 40-60% of patients treated.

In this trial, the investigators intend to study the interest of a treatment with epoetin beta in patients with anemia <10 g / dL in the context of a myelodysplastic syndrome with IPSS score <1.

In addition to studying the erythroid response, the investigators will measure the impact on quality of life and functional performance.

Patients will receive epoetin beta (60 000UI/week). Response will be assessed after 12 and 24 weeks of treatment.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Groupe Francophone des Myelodysplasies
• Treatments: Epoetin Alfa

Criteria

Inclusion Criteria:

• Written informed consent

• Must be 18 years of age or older at the time of screening

• Myelodysplastic Syndrome of the following subtypes : RA, RAS, RCMD, RCMD-RS, RAEB 1, with IPSS score low or intermediate 1 (IPSS score < 1 ) and with anemia defined by Hb < 10 g/dl (with RBC transfusion requirement or not)

• For women of childbearing potential, need for effective contraception throughout the study period.

Exclusion Criteria:

• Intensive Chemotherapy within 3 months before inclusion

• Myelodysplastic Syndrome with IPSS score >1

• Treatment with rHu-Epo or rHu-GCSF within 2 months before inclusion

• EGOG > 3 ;

• Other causes of anemia (eg. , Iron deficiency, vitamin B12 or folic acid, hypothyroidism before correction)

• Uncontrolled arterial hypertension

• Life expectancy less than 6 months

• CMML

• Pregnant or breast feeding female subjects

• Patients with creatinine clearance less than 30ml/min.