Trial Search Results

Pilot Lenalidomide in Adult Diamond-Blackfan Anemia Patients w/ RBC Transfusion-Dependent Anemia

This is a single-center, single arm, open-label study of oral lenalidomide monotherapy administered to red blood cell (RBC) transfusion dependent adult subjects with Diamond-Blackfan Anemia (DBA).

Primary Objective: To evaluate the erythroid response rate as measured by rate of red blood cell transfusion independence [MDS International Working Group (IWG) 2000 Criteria will be applied].

Secondary Objective: 1)To evaluate the tolerability and safety profile of lenalidomide in patients with DBA and other inherited marrow failure syndromes 2) To correlate response to lenalidomide with biologic surrogates of DBA including ribosomal protein mutation status, ex vivo erythroid colony growth, and microarray gene expression

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Jason Robert Gotlib

Collaborator: Celgene Corporation

Stanford Investigator(s):

Intervention(s):

  • Drug: Lenalidomide

Phase:

Phase 1

Eligibility


INCLUSION CRITERIA

   - Understand and voluntarily sign an informed consent form

   - Diagnosis of DBA

   - Age ≥ 18 years at the time of signing the informed consent form.

   - Able to adhere to the study visit schedule and other protocol requirements.

   - Red blood cell transfusion-dependent with a requirement of at least one unit of RBCs
   per month for the 2 months prior to study enrollment (eg, 2 units/8 weeks)

   - If applicable, ongoing therapy with a stable or decreasing dose of prednisone ≤ 60
   mg/d or corticosteroid equivalent, for which there has been no treatment-related
   improvement in RBC transfusion requirements for at least 2 months prior to study entry

   - Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 2 at study entry.

   - Laboratory test results within these ranges:

      - Absolute neutrophil count (ANC) ≥ 1500/uL

      - Platelet (Plt) count ≥ 100,000/uL

      - Serum creatinine ≤ 2.0 mg/dL

      - Direct bilirubin ≤ 1.5 mg/dL

      - Aspartate aminotransferase (AST) ≤ 2.5 x upper limit of normal (ULN)

      - Alanine aminotransferase (ALT) ≤ 2.5 x ULN

      - Disease-free of prior malignancies for ≥ 5 years with exception of currently
      treated basal cell, squamous cell carcinoma of the skin, or carcinoma "in-situ"
      of the cervix or breast

   - Females of childbearing potential (FCBP) must have a negative serum or urine pregnancy
   test with a sensitivity of ≥ 50 milli-International Units (MIU)/mL within 10 to 14
   days prior to and again within 24 hours of prescribing lenalidomide (prescriptions
   must be filled within 7 days) and must either commit to continued abstinence from
   heterosexual intercourse or begin 2 acceptable methods of birth control, one highly
   effective method and one additional effective method at the same time, at least 28
   days before she starts taking lenalidomide. FCBP must also agree to ongoing pregnancy
   testing. Men must agree to use a latex condom during sexual contact with a FCBP even
   if they have had a successful vasectomy

   - Able to take aspirin (81 to 325 mg) daily as prophylactic anticoagulation (patients
   intolerant to aspirin may use warfarin or low molecular weight heparin)

EXCLUSION CRITERIA

   - Any serious medical condition, laboratory abnormality, or psychiatric illness that
   would prevent the subject from signing the informed consent form.

   - Pregnant or breast feeding females. (Lactating females must agree not to breast feed
   while taking lenalidomide)

   - 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

   - Use of any other experimental drug or therapy (excluding steroids) specifically used
   for DBA within 28 days of baseline including metoclopramide, leucine, danazol, or
   other hormonal therapy

   - Clinically significant anemia due to factors such as iron, B12, folate deficiencies,
   autoimmune or hereditary hemolysis, or gastrointestinal bleeding.

   - Known hypersensitivity to thalidomide

   - The development of erythema nodosum if characterized by a desquamating rash while
   taking thalidomide or similar drugs

   - Any prior use of lenalidomide

   - Concurrent use of other anti-cancer agents or treatments

   - Known positive for HIV or infectious hepatitis, type A, B or C

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting