Study of Granulocyte-Macrophage Colony-Stimulating Factor (GM-CSF) for Patients With Rising Prostate-Specific Antigen (PSA)
Status: | Active, not recruiting |
---|---|
Conditions: | Prostate Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | Any |
Updated: | 4/21/2016 |
Start Date: | April 1999 |
End Date: | December 2016 |
A Phase II Study of Granulocyte-Macrophage Colony-Stimulating Factor (GM-CSF) for the Treatment of Patients With Evidence of Serologic (PSA) Progression After Definitive Therapy for Localized Prostate Cancer
This is a Phase II study to test the efficacy of exogenously administered GM-CSF in prostate
cancer patients who have failed definitive local therapy, and have only serologic (PSA)
evidence of progression.
cancer patients who have failed definitive local therapy, and have only serologic (PSA)
evidence of progression.
Inclusion Criteria:
- Histologic diagnosis of adenocarcinoma of the prostate; stage T1-T3, N0-N1, M0
- Prior definitive therapy for primary prostate cancer consisting of:external beam
radiotherapy;brachytherapy with or without pelvic external beam radiation; or radical
prostatectomy with or without adjuvant or salvage radiation therapy
- Therapeutic PSA response to primary therapy below 1.0 ng/ml post radiation therapy or
below 0.4 ng/ml for radical prostatectomy
- Patients treated with adjuvant or salvage radiation therapy following radical
prostatectomy are eligible provided:Post prostatectomy PSA was never > 6.0 ng/ml,
last effective day of androgen deprivation is at least 3 months prior to study entry
- Recurrent PSA level elevation (between 0.4 ng/ml and 6.0 ng/ml) on two determinations
at least one week apart.
- No clinical evidence of gross local recurrence or known metastatic disease other than
PSA elevation. Transrectal ultrasound and/or biopsy to evaluate local recurrence is
not required. All patients will receive a bone scan and CT scan of the abdomen to
exclude metastases.
- Estimated life expectancy of at least 6 months.
- ECOG Performance status of 0 or 1.
- Willing and able to give informed consent.
Exclusion Criteria:
- Cryosurgery as definitive therapy of primary tumor.
- Any metastasis.
- No concurrent or prior malignancy is allowed except for the following: adequately
treated basal or squamous cell skin cancer, adequately treated Stage I or II cancer
from which the patient is currently in complete remission, or any other cancer from
which the patient has been disease-free for 5 years.
- Current systemic steroid therapy (inhaled or topical steroids acceptable).
- Prior hormonal therapy for treatment of progressive disease.
- Prior chemotherapy, immunotherapy, or therapy with other experimental agents for
prostate cancer.
- Any surgery within the prior 4 weeks.
- Bilirubin and SGOT > 2 x upper limit of normal.
- BUN and serum creatinine > 2.0 times normal.
- No active congestive heart failure.
- If there is a history of clinically significant obstructive airway disease, a DLCO
must exceed 50%.
- Active uncontrolled bacterial, viral or fungal infection until these conditions are
corrected or controlled.
- Any underlying medical condition which in the principal investigator's opinion will
make the administration of GM-CSF hazardous or obscure the interpretation of adverse
events.
- PSA > 6.0 ng/ml
We found this trial at
1
site
1600 Divisadero Street
San Francisco, California 94115
San Francisco, California 94115
888.689.8273
UCSF Helen Diller Family Comprehensive Cancer Center UCSF’s long tradition of excellence in cancer research...
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