Castration Compared to Castration Plus Metformin as First Line Treatment for Patients With Advanced Prostate Cancer



Status:Completed
Conditions:Prostate Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:5/24/2018
Start Date:April 2011
End Date:September 2016

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Phase II, Randomized, Placebo Controlled, Double Blind, Prospective Study of Castration Compared to Castration Plus Metformin as First Line Treatment for Patients With Advanced Prostate Cancer.

Prostate cancer is the most common non-cutaneous cancer in men. Patients with recurrent or
metastatic prostate cancer are treated with androgen-deprivation therapy, often termed
castration therapy. While the short and medium term benefits of castration are clear in
relation to therapeutic efficacy in patients with prostate cancer, it is now appreciated that
the resulting hypogonadism associated with castration is responsible for adverse consequences
or metabolic syndrome that include increase in body mass index (BMI) and fat mass,
hyperinsulinemia and insulin resistance, hyperlipidemia, reduced lean body mass (LBM) and
muscle strength, osteoporosis, sexual dysfunction, poor quality of life and higher
cardiovascular mortality. Lower testosterone levels in men independently predict the
development of metabolic syndrome. Low testosterone levels in men are associated with insulin
resistance and diabetes. Metformin is commonly prescribed for the treatment of type II
diabetes because it lowers both glucose and insulin levels. Studies show preliminary evidence
that metformin might have both antineoplastic and chemopreventative activity. Castration
therapy decreases insulin sensitivity, adversely alters lipid profiles and results in weight
gain, and it may be associated with a greater incidence of diabetes and cardiovascular
disease. Little is known about the optimal strategy to mitigate the adverse metabolic effects
of castration in men with prostate cancer. The rationale for using metformin in castrated men
with advanced prostate cancer stems from the observation that castration therapy is
associated with the metabolic syndrome, hyperinsulinemia and insulin resistance. Furthermore,
reports that hyperinsulinemia stimulates insulin receptor expression on prostate cancer
leading to tumor growth and development of castrate resistant prostate cancer suggest
metformin through its activation of the AMPK-LKBI pathway reduces liver gluconeogenesis
secondarily decreasing insulin levels may circumvent tumor growth and resistance to
castration therapy. More importantly, evidence that metformin inhibits the mTOR pathway
implicates an added therapeutic benefit as an anti-cancer agent.


Inclusion Criteria:

(Eligible subjects must meet one of the inclusion criteria 1-3 and all of items 4-6)

1. Men with metastatic prostate cancer that require castration therapy with either using
an LHRH analogue or surgical castration are eligible. Complete androgen blockade using
anti-androgen therapy prior to castration or up to 4 weeks following castration
therapy is permitted to prevent disease flare. Thereafter anti-androgen therapy may
continue or be discontinued based on treating physicians preference.

OR

2. Any men with prostate cancer who are candidates for castration therapy despite no
evidence of definite metastatic disease including patient with biochemical failure or
'rising PSA' are also permitted to enter study provided castration therapy is planned
for a minimum of a year. Patients with biochemical failure prior to enrolment should
have also have already received appropriate salvage therapy. Men with prostate cancer
who have already started castration therapy are also permitted to enter study provided
castration therapy was initiated within one month of study entry.

OR

3. Men with prostate cancer previously treated with castration therapy for management of
localized prostate cancer in the adjuvant setting or in combination with radiation
therapy are permitted to enter study provided they currently have known metastatic
disease and have non-castrate testosterone levels (Testosterone > 50 ng/dL).

4. An ECOG performance status of 0-2.

5. Patients will need to have documentation of metastatic disease in bone and/or soft
tissue, and a baseline PSA of ≥ 5 ng/ml. If patients have already had castration
therapy, their baseline PSA value will be reflective of the value prior to castration.
Patients with biochemical failures, with rising PSA (baseline PSA does not need to be
≥ 5 nglml to be eligible), without metastatic disease are also eligible if castration
therapy is indicated for minimum of 7 months and for these patients any PSA value is
permitted.

6. Patients must have provided informed consent, be willing to have blood specimens
taken, and exhibit no severe other medical or psychiatric problems.

Exclusion Criteria:

1. Patients with severe medical or psychiatric diseases are INELIGIBLE. (Patients with
stable chronic diseases such as high cholesterol or hypertension ARE eligible.)
Examples of problems that would make patients INELIGIBLE include severe heart failure,
or hypoxia due to severe lung disease.

2. Patients with clinical or biochemical evidence of renal failure or liver failure are
INELIGIBLE. Creatinine and bilirubin needs to be less than or equal to 1.3~up per
limit of normal (ULN), and ASTIALT less than or equal to 2.5 x ULN unless liver
metastasis is present then up to 5 X ULN permitted).

3. Patients already receiving metformin or anti-diabetic medications are INELIGIBLE.

4. If any patient develops symptomatic diabetes requiring drug therapy, he must receive
such a therapy, which may include metformin. This must be documented, and the patient
will not continue on the study.

5. Patients with important infections requiring antibiotics are INELIGIBLE, but patients
who acquire minor infections while on the study may remain on the study.

6. Alcohol abuse problems make patients INELIGIBLE. Patients need to be consuming less
than or equal to 14 units of alcohol weekly.

7. Patients with history or evidence of lactic acidosis or metabolic acidosis will be
excluded.
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