Adjuvant I.V. Iron Therapy During Erythropoetin Treatment of Anemic Patients With Lymphoproliferative Disorders.

S

Sundsvall Hospital

Status and phase

Completed
Phase 3

Conditions

Anemia
Multiple Myeloma
Chronic Lymphocytic Leukemia
Non Hodgkin Lymphoma

Treatments

Drug: Neo-Recormon and Venofer

Study type

Interventional

Funder types

Other

Identifiers

NCT00145652
Dnr:151:2003/29970
1-Hedenus
Medical Products Agency

Details and patient eligibility

About

This is a multi-center open label, randomized phase-3 study with stratification according to diagnosis and baseline serum-EPO level. The correction of mild or moderate anemia and the effect on iron kinetics by the rHuEPO treatment with or without intravenous iron supplementation in anemic patients with LPD not receiving antineoplastic therapy will be studied. The study will be performed according to the ICH-GCP guidelines. In order to be eligible, the patient must consent in writing that he/she agrees to participate in the study. The patient recruitment period is estimated to be no longer than 18 months.

Full description

In this multi-center, randomized, open label phase-3 study, the correction of mild or moderate anemia and the effect on iron kinetics by rHuEPO treatment, with or without intravenous iron treatment, in patients with LPD not receiving antineoplastic therapy will be studied. LENGTH OF STUDY 16 weeks NUMBER OF CENTERS 15 NUMBER OF SUBJECTS 66 STRATIFICATION 1. According to diagnosis; CLL and indolent NHL vs. MM. 2. According to level of S-epo > 100 IU/L vs £ 100 IU/L at baseline. TREATMENT The patients will be randomized to receive 30 000 IU Neorecormon â (epoetin beta) s.c. once / week for 16 consecutive weeks +/- 100mg/week of Venofer â (iron sucrose) from week 0 to 6, followed by one 100mg dose every 2 week from weeks 8 until 14. If the increase in Hb concentration is less than 10g/L from baseline (week 0) until week 4 weeks, the dose of epoetin beta will be increased to 60 000 IU weekly from week 5. If the Hb concentration exceeds 140 g/L, the epoetin beta therapy will be suspended. The treatment will be resumed once the Hb concentration falls below 130 g/L. This resumed dose will be 75% of the previous dose (e.g. if the previous dose was 30 000 IU before suspension, the continued dose should be 22 500 IU. If the dose was 60 000 IU before suspension, the dose should be 45 000 IU). If the level of S-ferritin reaches >1000 ug/L iron sucrose should be suspended until the S-ferritin level falls below 500 ug/L.

Sex

All

Ages

18+ months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Multiple myeloma, indolent NHL or CLL
  • Anemia of cancer with a Hb concentration within the range ³ 90 - £ 110 g/L measured at two different occasions with at least two weeks interval but inclusion within 4 weeks after the first Hb measurement.
  • Age >18 years.
  • Informed consent in writing.
  • Demonstration of stainable iron in bone-marrow aspirate.

Exclusion criteria

  • Planned or expected antineoplastic therapy (except systemic low dose maintenance corticosteroids) within the 6 weeks following inclusion.
  • Cytostatic or any other antitumor therapy (except systemic low dose maintenance corticosteroids) within 8 weeks before inclusion.
  • RBC transfusion within 8 weeks before inclusion.
  • RHuEPO treatment within 12 weeks before inclusion.
  • Any iron therapy within 4 weeks before inclusion.
  • Ongoing infectious disease.
  • Active inflammatory disease other than the malignant disease.
  • Performance status ³ 3 according to the ECOG scale.
  • Folate deficiency (S-folate < 4,5 nmol/L).
  • B12 deficiency (S-cobalamin < 145 pmol/L).
  • Ongoing haemolysis defined as S-haptoglobin < 0,2 g/L
  • Impaired kidney function (S-Creatinine > 175 mmol/L)
  • Acute or chronic clinical relevant hepatic dysfunction (S-bilirubin >40 umol/L)
  • S-Ferritin >800 ug/L
  • Ongoing significant neurological or psychiatric disorders including psychotic disorders or dementia.
  • Unstable or uncontrolled disease related to or affecting cardiac function e.g., unstable angina, congestive heart failure (NYHA>Class ll), uncontrolled hypertension (diastolic BP >100 mmHg) and/or uncontrolled cardiac arrhythmia.
  • Known history of allergy to any of the study medications or their excipients.
  • Concurrent treatment with experimental drugs not approved by Läkemedelsverket.
  • Male and female patients with reproductive potential must use an approved contraceptive method (e.g. intrauterine device (IUD), birth control pills or barrier device) during the study and for 3 months after the study. Females with childbearing potential must have a negative serum pregnancy test within 7 days prior to study enrolment.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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