Study of Lenalidomide and Docetaxel in Subjects With Androgen Independent Prostate Cancer

Columbia University

Status and phase

Completed

Phase 1

Conditions

Prostate Cancer

Treatments

Drug: Docetaxel

Drug: Lenalidomide

Drug: Prednisone

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01378091

AAAB3212

Details and patient eligibility

About

Primary objectives:

To determine the maximum tolerated doses (MTDs) of daily lenalidomide and docetaxel given every three weeks and prednisone, as combination therapy to subjects with androgen independent prostate cancer

To evaluate the safety profile of the combination of daily lenalidomide and every three week docetaxel and prednisone when given to subjects with androgen independent prostate cancer

Secondary objective:

To explore the anti-tumor activity of the combination of daily lenalidomide and every 3 week docetaxel and prednisone when given to subjects with androgen independent prostate cancer.

Full description

Adenocarcinoma of the prostate is the second leading cause of cancer death in men. There is medication available to help treat this disease, which typically lengthens life by 10 to 12 months. More recent studies have shown average survivals of 20 to 23 months.

The investigators hope that the experimental (research) drug called lenalidomide (Revlimid®), which is being used in this study, will lengthen the lives of these patients by even more time. A different drug in the same drug family has demonstrated activity against a variety of solid tumors as well as hematological malignances. It works against cancer in different ways than chemotherapy by affecting the immune system (the body's ability to naturally fight disease).

The investigators believe that the study drug helps build up patients' immune systems than some of the other popular drugs on the market, and may potentially increase survival rates for patients with hormone refractory prostate cancer.

Enrollment

64 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subjects must understand and voluntarily sign an informed consent document.
Age > 18 years at the time of signing informed consent form.
Histological documentation of prostate cancer.
Subjects must be able to adhere to the study visit schedule and other protocol requirements.
Radiographic or clinical evidence of measurable or evaluable androgen independent prostate cancer stages D1 or D2.
Patients must be surgically or medically castrated. If the method is medical castration, the patient must have a serum testosterone level of <50 ng/dl/. The patient should maintain treatment with LH RH antagonists or agonists.
Patients must have metastatic prostate cancer unresponsive or refractory to androgen blockade by one or more of the following criteria:
- Progression of unidimensionally measurable disease.
- Progression of non measurable disease
- Rising PSA (absolute value of PSA > 5 mg/ml).
- Rising PSA is defined as at least 2 consecutive rises in PSA to be documented over the reference value (measure 1). The first rising PSA (measure 2) must be taken at least 7 days after the reference value. A third confirmatory PSA is required, and it must be obtained at least seven days after the second measure. If the third measure does not confirm the rise in PSA, a fourth PSA measure is required to be taken to confirm the rise over the second measure.
Patients who were treated with antiandrogens such as flutamide, or other hormonal agents such as estrogens, or ketoconazole must have been stopped for at least 28 days prior to enrollment. In the case of nilandron and bicalutamide, treatment with these agents must have stopped at least 42 days prior to treatment. If the patient is being treated with corticosteroids, the dose should be stable for 14 days prior to study entry
ECOG performance status of ≤2 (Appendix I: ECOG Performance Status Scale).
Regarding Lenalidomide: Men must agree to use a latex condom during sexual contact with a FCBP even if they have had a successful vasectomy. All patients must be counseled at a minimum of every 28 days about pregnancy precautions and risks of fetal exposure. See Appendix V: Risks of Fetal Exposure, Pregnancy Testing Guidelines and Acceptable Birth Control Methods, AND also Appendix VI: Education and Counseling Guidance Document.
Laboratory values as indicated below:
- Serum Creatinine <2.0 mg/dL
- Absolute Neutrophil Count ≥1,500/mm3 (or 1.5 X109/L)
- Platelet Count >100,000/mm3 (or 100 x 109/L)
- Aspartate Aminotransferase (AST/SGOT) ≤ 1.5 x upper limit of normal (ULN)
- Alkaline Phosphatase < 2.5 x ULN (In the absence of liver metastasis, elevated alk phos due to bone mets is permitted)
- Conjugated Bilirubin < ULN

Exclusion criteria

Any serious medical condition or psychiatric illness that places the subject at an unacceptable risk for study participation or would prevent the subject from signing the informed consent.
More than 2 prior regimens of chemotherapy.
Use of thalidomide or biologic response modifier therapy within 28 days of initiation of therapy
Prior desquamating rash while taking thalidomide therapy.
Prior > grade-2 allergic reaction to thalidomide.
Any prior use of lenalidomide. Subjects may have received prior thalidomide therapy.
Concurrent use of any other anti-cancer agents, excluding bisphosphonates.
Known brain or leptomeningeal disease (CT scan or MRI of the brain required only in case of clinical suspicion of central nervous system involvement).
Active infection, known positive for HIV or hepatitis B or C.
Known hypersensitivity or intolerance to taxanes or polysorbate 80.
Known hypersensitivity reaction to thalidomide
Use of any other experimental drug or therapy within 28 days.
Subjects with > grade-2 neuropathy.
Prior history of malignancy (except basal cell or squamous cell carcinoma or carcinoma in situ of the breast, or superficial bladder cancer) unless the subject has been free of disease for > 3 years.
Prior whole pelvic radiation, or prior treatment with strontium. Prior treatment with samarium is permitted.