| Eligibility |
Inclusion
- Patients must have a histologically confirmed diagnosis of adenocarcinoma of the
prostate that is hormone refractory and with evidence of progressive metastatic
disease following docetaxel treatment by any of the following:
- Increased serum prostate-specific antigen (PSA) levels confirmed by 3 consecutive
PSA measurements (at least 2 weeks apart), the first sample to be taken at least
6 weeks after bicalutamide or megestrol acetate withdrawal AND/OR
- Progression of bidimensionally measurable soft tissue (nodal) metastasis by CT
scan or MRI within the past 4 weeks AND/OR
- Progression of bone disease by at least two new bone lesions on bone scan
confirmed by a second bone scan
- Patients should be without persisting >= grade 2 hematological/non-hematological
toxicities from previous treatments that would preclude evaluation of toxic effects of
study treatment.Grade 1 residual toxicity will be acceptable. Patients should be off
prior therapies at least 4 weeks before starting study treatment
- Prior palliative radiation to metastatic lesion(s) is permitted, provided there is at
least one measurable and/or evaluable lesion(s) that has not been radiated
- Castrate levels of serum testosterone (=< 50 ng/dL or 1.0 mmol/L) confirmed within two
weeks prior to Day 1 of treatment. Testosterone levels will not be required for
patients who have had bilateral orchiectomy
- ECOG performance status 0-1
- Life expectancy of greater than 6 months
- Absolute neutrophil count >= 1,500/mm^3
- Platelets >= 100,000/mm^3
- Hgb >= 9g/L
- Total bilirubin =< 1.5 x laboratory upper limit of normal (ULN)
- AST(SGOT)/ALT(SGPT) <= 2.5 x laboratory ULN
- Creatinine =< 1.5 x laboratory ULN or calculated creatinine clearance >= 50 ml/min
- Serum amylase =< ULN (If > ULN, confirm pancreatic amylase < 1.1 ukat/L and serum
lipase < ULN)
- PT/INR <= 1.5
- Urine protein < 1+ or if >= 1 then 24-hour urine protein should be obtained and should
be < 1000 mg
- Serum cholesterol < ULN with or without treatment for hyperlipidemia; if > ULN and
untreated, may be rescreened for eligibility after treatment
- Eligibility of patients receiving any medications or substances known to affect or
with the potential to affect the activity or pharmacokinetics of temsirolimus will be
determined following review of their case by the Principal Investigator
- Patients, if sexually active, will agree to use adequate contraceptive methods
(barrier contraceptive with spermicide, vasectomy, abstinence) prior to study entry
and for the duration of study participation
- Ability to understand and the willingness to sign a written informed consent document
- No evidence (>= 5 years) of prior malignancies except successfully treated basal cell
or squamous cell carcinoma of the skin
Exclusion
- Prior use of HDAC or mTOR inhibitors
- Patients with known brain metastases
- Any medical condition, including the presence of laboratory abnormalities, which
confounds the ability to interpret data from the study or places the patient at
unacceptable risk if he participates in the study
- History of allergic reactions attributed to compounds of similar chemical or biologic
composition to vorinostat or temsirolimus
- Concurrent use of other anticancer agents or treatments except LHRH antagonists
- Uncontrolled intercurrent illness including, but not limited to the
following:(a)Ongoing or active infection including viral hepatitis,(b)Symptomatic
congestive heart failure (New York Association Class II, III, or IV),(c) unstable
angina pectoris requiring nitrate therapy,(d) prior myocardial infarction,(e)severe
uncontrolled ventricular cardiac arrhythmias,(f) uncontrolled hypertension (defined as
blood pressure of > 160 mmHg systolic and/or > 90 mmHg diastolic on
medication),(g)electrocardiographic evidence of acute ischemia(h)Psychiatric
illness/social situations that would limit compliance with study requirements
- Known positive serology for HIV and known history of HIV because of the potential for
pharmacokinetic unforeseen toxicity and morbidity in an immunocompromised patient
- Any treatment modalities, including radiation and surgery, not discontinued at least 4
weeks prior to treatment in this study
- Chronic Hepatitis with advanced, decompensated hepatic disease or cirrhosis of the
liver or history of chronic virus hepatitis or known viral hepatitis carrier (patient
recovered from Hepatitis A will be allowed to enter the study)
- Simultaneous participation in any other study involving investigational drugs or
having participated in a study less than 4 weeks prior to treatment in this study
- No investigational or commercial agents or therapies other than those described in the
study may be administered with the intent to treat the patient's malignancy
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