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Study Summary
No. 2003-0922:.......Prostate......Shi-Ming Tu......Genitourinary Medical Oncology
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Study Summary Title
Study Summary
Number:
2003-0922
Study Title:A Randomized Phase II Study of Bone Targeted Therapy in Metastatic Androgen-Dependent Prostate Cancer
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Physician New Patient Referral
Name:Shi-Ming TuPatients Call:800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Dept:Genitourinary Medical OncologyReferring MD
Call:
800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Phone:713-792-2830
Contact us about clinical trials
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General Information
Disease Group:ProstateSupported By:N/A
Phase of Study:Phase IIReturn
Visit:
Patients will have up to 10 weekly treatment visits and will be followed
indefinitely.
Treatment
Agents:
Doxorubicin
Strontium 89 Chloride
Zoledronic acid
Home Care:NA
Treatment Loc:MDACC + Community Programs (CCOP/Network)
Estimated
Length of Stay
in Houston:
NA
Description/
Intervention:
The goal of this clinical research study is to find out what added effects
(good and bad) Metastron® (strontium-89) has on your prostate cancer and the
spread of your cancer to your bones when given after different standard
treatments.
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Study Objectives / Outcomes
1. Determine the clinical efficacy, as measured by progression-free survival, of hormonal ablative therapy combined with zoledronic acid and doxorubin with or without strontium-89 for patients with androgen-dependent prostate cancer and bone metastases.

Randomization will occur in two arms:
Arm 1: Strontium-89 in combination with Doxorubicin and Zoledronic acid
Arm 2: No Strontium-89 in combination with Doxorubicin and Zoledronic acid

2. Collect serial sera and urine for the study of bone-epithelial markers and collagen crosslinks.
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Study Status Information
Study Activation / Registration Date:07/06/2004
IRB Review and Approval Date:01/07/2004
Study Type:Therapeutic
Recruitment Status:Closed
Projected Accrual:80
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Enrollment Eligibility
If you do not meet the enrollment eligibility, there may be other treatment options for you. Please Contact the Referral Office for more information.

Inclusion Criteria:1) Histologically or cytologically confirmed prostate carcinoma.

2) Osteoblastic metastases on bone scan or CT scan.

3) Initiation of hormonal ablative therapy within 3 months of registration.

4) Prior neoadjuvant, concurrent, or intermittent hormonal ablative therapy of less than 3 years duration and completed at least 3 years prior to entry into this study.

5) ECOG performance status <3 (Karnofsky >40%)

6) Patients must have normal organ and marrow function as defined: leukocytes: >3,000/mL; absolute neutrophil count: >1,500/mL; platelets: >100,000/mL; total bilirubin within normal institutional limits; AST(SGOT)/ALT(SGPT): <2.5 X institutional upper limit of normal; creatinine: < or = 3.0; left ventricular ejection fraction: >45%

7) The effects of strontium-89 and zoledronic acid on the developing human fetus at the recommended therapeutic dose are unknown. Even though all patients are castrated during this study, men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should the spouse of a patient become pregnant or suspect she is pregnant while participating in this study, she/he should inform the treating physician immediately.

8) Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:1) More than one prior chemotherapy regimen. Prior doxorubicin treatment is permitted. However patient's with >250 mg/m2 cumulative dosage are excluded.

2) Prior radioisotope treatment consisting of strontium-89 or samarium-153.

3) Zoledronic acid treatment for more than 3 months duration prior to registration. Other bisphosphonate treatments are permitted.

4) Corrected serum calcium level less than 8 mg/dL.

5) Patients may not be receiving any other investigational agents.

6) Patients with known brain metastases should be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events.

7) History of allergic reactions attributed to compounds of similar chemical or biologic composition to zoledronic acid or other agents used in the study

8) Patients with the following atypical presentations should have a biopsy: those with small cell carcinoma, purely lytic bone metastases, or bulky (i.e. 5 cm) visceral or nodal disease in the absence of bone involvement are not eligible.

9) Symptomatic bulky lymphadenopathy causing scrotal or pedal edema or significant local invasive disease in bladder invasion.

10) History of other malignancies other than nonmelanoma skin cancer, unless in complete remission and off therapy for that disease for at least 5 years.

11) Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, history of congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.

12) Because patients with immune deficiency are at increased risk of lethal infections when treated with marrow-suppressive therapy, HIV-positive patients receiving combination anti-retroviral therapy are excluded from the study because of possible pharmacokinetic interactions with strontium-89 or other agents administered during the study. Appropriate studies will be undertaken in patients receiving combination anti-retroviral therapy when indicated.

13) Evidence or suspicion of myelodysplastic syndrome by CBC must be confirmed by bone marrow biopsy.

14) Untreated symptomatic spinal cord compressions.

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Links
Registration Number: NCT00081159
Study Information on Clinical Trials Registry (clinicaltrials.gov)

Other Links:
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Results


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