Safety and Efficacy Study of GM-CSF, Thalidomide Plus Docetaxel in Prostate Cancer

Inclusion Criteria:

Diagnosis of adenocarcinoma of the prostate.
Failure of local treatments (surgery and/or radiation) as defined by a rising PSA; demonstrated by at least three consecutive rises in PSA by intervals of at least 4 weeks apart with an absolute change of at least 1 ng/mL. If the confirmatory PSA (third PSA) is less than the previous screening PSA value, an additional test for rising PSA will be required to document progression.
No clinical or radiographic evidence of disease.
The Zubrod performance status 0-1.
Prior hormonal therapy in the form of neoadjuvant or adjuvant therapy is allowed as long as androgen therapy has been completed at least 1 year prior to study entry.
Adequate hematologic function: absolute granulocytes ≥ 1500/ul, platelets ≥ 100,000/ul, hemoglobin ≥ 10 gm/100 ml within 4 weeks prior to study entry.
Adequate hepatic function: bilirubin ≤ 1.5 mg/dl, liver enzymes ≤ 1.5 ULN within 4 weeks prior to study entry.
Adequate renal function: creatinine ≤ 1.5 x ULN within 4 weeks prior to study entry.
Patients treated with bisphosphonate therapy before or after study entry are eligible to continue in the study.
Negative bone scan within 6 weeks prior to study entry.
Negative CT scan or MRI of the abdomen and pelvis within 6 weeks prior to study entry.
Negative chest x-ray for metastatic disease within 6 weeks prior to study entry.
Patients must sign a written informed consent prior to treatment.

Exclusion Criteria:

Serious intercurrent medical illness including symptomatic heart disease within 6 months.
Previous or concurrent invasive cancers other than superficial non-melanomatous skin cancer unless disease-free for at least 5 years.
Major medical or psychiatric illness which, in the investigator's opinion, would prevent completion of treatment and would interfere with follow-up.
History of thromboembolic events (deep venous thrombosis, symptomatic cerebrovascular events or pulmonary embolism), history of MI, within the last 12 months.
History of bleeding disorders that would contraindicate Coumadin® (warfarin) including: esophageal varices and clotting factor defects