Overview

This trial is active, not recruiting.

Condition multiple myeloma light chain induced renal insufficiency
Treatment lenalidomide plus dexamethasone
Phase phase 2
Sponsor Austrian Forum Against Cancer
Start date May 2009
End date May 2014
Trial size 50 participants
Trial identifier NCT00902915, LD

Summary

The purpose of this study is to determine efficacy of lenalidomide and dexamethasone in the treatment of patients with acute Myeloma (light chain)-induced renal failure.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Endpoint classification safety/efficacy study
Intervention model single group assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
lenalidomide plus dexamethasone
peroral application; lenalidomide dosage according to severity grade of renal failure.

Primary Outcomes

Measure
To determine the response rate (CR, VGPR, PR, MR, SD, and PD) To determine the renal response rate To determine the relation between category of myeloma response and improvement in GFR To determine the proportion of patients spared hemodialysis
time frame:

Secondary Outcomes

Measure
Progression Free Survival, Event Free Survival, Overall Survival; Toxicity, evaluated according to the NCCN toxicity scale (type, frequency, severity, and relationship of adverse events to study treatment).
time frame:

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria: - Understand and voluntarily sign an informed consent form. - Age at least 18 years at the time of signing the informed consent form. - MM (all stages) with acute light chain induced renal impairment - Patients with previously unknown MM and acute light chain induced renal failure (GFR<50ml/min and serum creatinine minimum 2.0 mg/dL) and with further workup revealing light chain induced renal injury with MM as underlying cause. - Patients with previously established MM and normal renal function (GFR ≥60ml/min and serum creatinine ≤1.2mg/dl) with progressive disease and acute (within 6 weeks) light chain induced renal failure (GFR<50ml/min and creatinine ≥ 2.0 mg/dL). - Disease progression will be documented by one or more of the following criteria: - Increase in serum paraprotein by >25%, or increase of 50% of 24 hour urine paraprotein excretion - Hypercalcemia - Progression of bone lesions - Decrease in Hb>2g/dl within 4 weeks (not induced by cytotoxic drugs) - Increase in bone marrow plasma cell infiltration by > 25% - All previous medical anti-myeloma therapy (excluding corticosteroids) must have been discontinued at least 3 weeks prior to treatment in this study. - Able to adhere to the study visit schedule and other protocol requirements. - Measurable serum or urine paraprotein - Laboratory test results within these ranges: - Glomerular filtration rate < 50ml/min - Serum creatinine ≥ 2.0mg/dL - Absolute leukocyte count ≥ 1.5 x 10G/L - Platelet count minimum 75 x 10G/L if bone marrow plasma cell infiltration (BMPC) is ≥50% or minimum 30 x 10G/L if BMPC infiltration is <50%. - Total bilirubin minimum 1.5 mg/dL - AST (SGOT) and ALT (SGPT) not more than 2,5 x ULN - Females of childbearing potential (FCBP) must: - Understand that the study medication could have an expected teratogenic risk - Agree to use, and be able to comply with, effective contraception without interruption, 4 weeks before starting study drug, throughout study drug therapy (including dose interruptions) and for 4 weeks after the end of study drug therapy, even if she has amenorrhea. This applies unless the subject commits to absolute and continued abstinence confirmed on a monthly basis. The following are effective methods of contraception: Implant, Levonorgestrel-releasing intrauterine system (IUS, Medroxyprogesterone acetate depot), Tubal sterilization, Sexual intercourse with a vasectomised male partner only; vasectomy must be confirmed by two negative semen analyses Ovulation inhibitory progesterone-only pills (i.e., desogestrel) - Agree to have a medically supervised pregnancy test with a minimum sensitivity of 25 mIU/ml not more than 3 days before the start of study medication once the subject has been on effective contraception for at least 4 weeks. This requirement also applies to women of childbearing potential who practice complete and continued abstinence. - Agree to have a medically supervised pregnancy test every 4 weeks including 4 weeks after the end of study treatment, except in the case of confirmed tubal sterilization. These tests should be performed not more than 3 days before the start of next treatment. This requirement also applies to women of childbearing potential who practice complete and continued abstinence. - Male subjects must: - Agree to use condoms throughout study drug therapy, during any dose interruption and for 28 days after cessation of study therapy if their partner is of childbearing potential and has no contraception. - Agree not to donate semen during study drug therapy and for 28 days after end of study drug therapy. - All subjects must agree not to share study medication with another person and to return all unused study drug to the investigator - Disease free of prior malignancies for minimum of 3 years with exception of currently treated basal cell, squamous cell carcinoma of the skin, or carcinoma "in situ" of the cervix or breast - Agree to take low molecular weight heparin as prophylactic anticoagulation. Exclusion Criteria: - Acute renal failure due to other causes than light-chain induced nephropathy such as NSAIRS, antibiotics, or other nephrotoxic drugs, or others. - Acute renal failure due to hypercalcemia only, without excretion of nephrotoxic light chains. - Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form. - Any prior use of lenalidomide - Any anti-myeloma therapy within 3 weeks before day 1 of first cycle, with the exception of dexamethasone 40mg (maximum dose 160mg) or corticosteroid equivalent. - Any other experimental drug or therapy within 3 weeks of baseline - Any condition, including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study. - The development of erythema nodosum if characterized by a desquamating rash while taking thalidomide or similar drugs. - Known positive for HIV or infectious hepatitis, type A, B or C or evidence of any severe active or chronic infection. - Clinical significant heart disease (NYHA status>2) - Pregnant or breast feeding females - Anamnesis of thromboembolic complications, such as stroke, myocardial infarction and pulmonary embolism

Trial information was received from ClinicalTrials.gov and was last updated in November 2013.
Information provided to ClinicalTrials.gov by Austrian Forum Against Cancer.