Trial Search Results

Radium-223 Dichloride (BAY88-8223) in Castration-Resistant (Hormone-Refractory) Prostate Cancer Patients With Bone Metastases

This study is a prospective, interventional, open-label, multi-center early access program for the use of Ra-223 Cl2 in HRPC/CRPC patients diagnosed with symptomatic bone metastasis and to collect additional short and long term safety data on the product.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Bayer

Intervention(s):

  • Drug: Radium-223 dichloride (BAY88-8223)

Eligibility


Inclusion Criteria:

   - Age ≥ 18 years

   - Histologically or cytologically confirmed prostate cancer

   - Patients diagnosed with symptomatic progressive bone predominant metastatic CRPC/HRPC
   with at least 2 skeletal metastases on imaging with no lung, liver, and/or brain
   metastasis (lymph node only metastasis is allowed)

   - Symptomatic is defined as either

      - Regular (not occasional) use of analgesic medication for cancer related bone pain
      (≥ level 1; World Health Organization [WHO] ladder for cancer pain), or

      - Treatment with external beam radiation therapy (EBRT) for bone pain (the EBRT
      should be within the last 12 weeks before treatment)

   - Progressive disease is defined either by:

      - The appearance of new bone lesions. If progression is based on new lesion(s) on
      imaging only without an increase in prostate specific antigen (PSA), then PSA
      values from 3 assessments within the last 6 months must be provided; OR

      - In the absence of new bone lesions, 2 subsequent increases in serum PSA over
      previous reference value, which should not be more than 6 months before
      screening, each measured at least 1 week apart with the last PSA ≥ 5 ng/mL. (The
      reference value time point 1, is defined as the last PSA measured before
      increases are documented, with subsequent values obtained a minimum of 1 week
      apart. If the PSA at time point 3 is greater than the PSA at time point 2, then
      eligibility has been met. If the PSA at time point 3 is not greater than the PSA
      at time point 2 but, the PSA value at time point 4 and/or time point 5 is greater
      than the PSA at time point 2, the patient is eligible assuming that other
      criteria are met).

   - No intention to use cytotoxic chemotherapy within the next 6 months

   - Life expectancy ≥ 6 months

   - Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0-2

   - Adequate hematological, liver, and renal function

      - Absolute neutrophil count (ANC) ≥ 1.5 x10^9/L

      - Platelet count ≥ 100 x10^9/L

      - Hemoglobin ≥ 10.0 g/dL (100 g/L; 6.2 mmol/L)

      - Total bilirubin level ≤ 1.5 x institutional upper limit of normal (ULN)

      - Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x ULN

      - Creatinine ≤ 1.5 x ULN

      - Albumin > 25 g/L *Any bone imaging techniques as per institutional standard of
      care

Exclusion Criteria:

   - Treatment with an investigational drug within previous 4 weeks, or planned during the
   treatment period or follow-up

   - Eligible for first course of docetaxel, i.e., patients who are fit enough, willing,
   and who are located where treatment with docetaxel is available

   - Treatment with cytotoxic chemotherapy within previous 4 weeks prior to screening, or
   failure to recover from adverse events (AEs) due to cytotoxic chemotherapy
   administered more than 4 weeks previous prior to screening (however, ongoing
   neuropathy is permitted)

   - Prior hemibody external radiotherapy is excluded. Patients who received other types of
   prior external radiotherapy are allowed provided that the bone marrow function is
   assessed and meets the protocol requirements for hemoglobin, absolute neutrophil
   count, and platelets

   - Received systemic therapy with radionuclides (e.g., strontium-89, samarium-153,
   rhenium-186, or rhenium-188, or radium-223 dichloride) for the treatment of bony
   metastases

   - Other malignancy treated within the last 3 years (except non melanoma skin cancer or
   low-grade superficial bladder cancer)

   - Visceral metastases as assessed by abdominal or pelvic computed tomography (CT) (or
   other imaging modality based on institutional standard of care)

   - Presence of brain metastases

   - Lymphadenopathy exceeding 6 cm in short-axis diameter

   - Any size pelvic lymphadenopathy if it is thought to be a contributor to concurrent
   hydronephrosis.

   - Imminent spinal cord compression based on clinical findings and/or magnetic resonance
   imaging (MRI). Patients with history of spinal cord compression should have completely
   recovered.

   - Any other serious illness or medical condition, such as but not limited to:

      - Any infection ≥ National Cancer Institute Common Terminology Criteria for Adverse
      Events (NCI-CTCAE) version 4.03 Grade 2

      - Cardiac Failure New York Heart Association (NYHA) Class III or IV

      - Crohn's disease or ulcerative colitis

      - Bone marrow dysplasia

   - Fecal incontinence

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

Male

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Cancer Clinical Trials Office
650-498-7061
Not Recruiting