Carboplatin, Everolimus, and Prednisone in Treating Patients With Metastatic Prostate Cancer That Progressed After Docetaxel

Prostate Cancer Clinical Trial

Official title:

Phase II Trial of Carboplatin and Everolimus (RAD001) in Metastatic Castrate Resistant Prostate Cancer (CRPC) Pretreated With Docetaxel Chemotherapy.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01051570
• Other study ID #: CDR0000663630
• Secondary ID: P30CA022453WSU-2
• Status: Completed
• Phase: Phase 2
• Start date: February 2010
• Est. completion date: September 2013

Study information

• Verified date: November 2020
• Source: Barbara Ann Karmanos Cancer Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Drugs used in chemotherapy, such as carboplatin and prednisone, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Everolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Giving carboplatin together with everolimus and prednisone may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving carboplatin together with everolimus and prednisone works in treating patients with metastatic prostate cancer that progressed after docetaxel.

Description:

OBJECTIVES:

Primary

• To evaluate the time to progression (TTP) achieved with carboplatin and everolimus in patients with castrate resistant metastatic prostate cancer that progressed after docetaxel-based chemotherapy.

Secondary

• To evaluate the safety of this regimen.

• To assess the PSA response rate in patients treated with this regimen.

• To evaluate the overall survival (OS) outcome in these patients.

• To investigate the association of TTP and PSA response rate with correlative markers, such as phospho mTOR, pAKT, and p70S6.

• To evaluate the pharmacokinetics of this regimen.

• To explore the association of TTP, OS, and circulating tumor tumor cell count.

OUTLINE: Patients receive carboplatin IV over 30-60 minutes on day 1, oral prednisone twice daily on days on days 1-21, and oral everolimus once daily on days 2-21 of course 1 and on days 1-21 of subsequent courses. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Blood and tumor tissue samples are collected periodically for pharmacodynamic, pharmacokinetic, and biomarker analysis.

After completion of study treatment, patients are followed up every 3 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 26
• Est. completion date: September 2013
• Est. primary completion date: September 2013
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 120 Years

Eligibility

DISEASE CHARACTERISTICS:

• Histologically confirmed metastatic adenocarcinoma of the prostate

• Objective disease progression or rising PSA despite androgen deprivation therapy and antiandrogen withdrawal (when applicable)

• Progressed after = 1 prior docetaxel-based chemotherapy regimen for metastatic disease

• Patients with measurable disease* must have either rising PSA, increase in size of the lesion(s), or both

• Patients with rising PSA as the only evidence of disease progression must demonstrate a rising trend with 2 successive elevations = 1 week apart

• Patients with no measurable disease must have a PSA = 5 ng/mL or new areas of bony metastases on bone scan NOTE: *There is no minimum PSA requirement for patients with measurable disease

• Documented to be castrate with a testosterone level of = 0.5 ng/mL

• Leuteinizing hormone-releasing hormone agonist therapy must be continued, if required to maintain castrate levels of testosterone

• No uncontrolled brain or leptomeningeal metastases, including patients who continue to require glucocorticoids for brain or leptomeningeal metastases

PATIENT CHARACTERISTICS:

• Zubrod performance status 0-1

• ANC = 1,500/mm^3

• Hemoglobin = 9.0 g/dL

• Platelet count = 100,000/mm^3

• Total bilirubin = 1.5 times upper limit of normal (ULN)

• Calculated creatinine clearance = 50 mL/min OR serum creatinine = 2 mg/dL

• AST and/or ALT = 2.5 times ULN if alkaline phosphatase normal OR alkaline phosphatase = 4 times ULN if AST and/or ALT normal (for patients without documented bone metastases or for patients with liver metastases)

• AST and/or ALT < 2.5 times ULN, without regard to alkaline phosphatase levels (for patients with documented bone metastases)

• Fasting serum cholesterol = 300 mg/dL OR = 7.75 mmol/L AND fasting triglycerides = 2.5 times ULN (in the case that one or both of these thresholds are exceeded, the patient is eligible only after initiation of appropriate lipid-lowering medication)

• Fertile patients must use effective contraception during and for = 6 months after completion of study treatment

• Willing and able to comply with this study

• Able to ingest oral medication

• No other malignancies except non-melanoma skin cancer or any other adequately treated cancer in complete remission for = 2 years

• No significant traumatic injury within the past 4 weeks

• No active (acute or chronic) or uncontrolled severe infections

• No severe and/or uncontrolled medical conditions or other conditions that could affect study participation, including the following:

• NYHA class III-IV symptomatic congestive heart failure

• Unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction within the past 6 months, serious uncontrolled cardiac arrhythmia, or any other clinically significant cardiac disease

• Severely impaired lung function as defined by spirometry and DLCO that is 50% of the normal predicted value and/or oxygen saturation that is = 88% at rest on room air

• Uncontrolled diabetes as defined by fasting serum glucose > 1.5 times ULN

• Liver disease such as cirrhosis, chronic active hepatitis, or chronic persistent hepatitis

• Known history of HIV seropositivity, hepatitis B or C

• Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of everolimus (e.g., ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection)

• Active, bleeding diathesis

• No known hypersensitivity to everolimus or other rapamycins (sirolimus, temsirolimus) or to their excipients

• No history of noncompliance to medical regimens

• No uncontrolled diabetes mellitus

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• At least 1 prior docetaxel based regimen for metastatic disease

• Docetaxel based combination therapy or docetaxel alone considered as 1 regimen

• No more than 2 prior chemotherapy regimens for metastatic disease

• No prior treatment with an mTOR inhibitor (sirolimus, temsirolimus, everolimus)

• At least 6 weeks since prior bicalutamide or nilutamide

• At least 4 weeks since prior flutamide

• More than 4 weeks since prior and no other concurrent investigational drugs

• More than 4 weeks since prior and no other concurrent anticancer therapies (including chemotherapy, radiotherapy, or antibody-based therapy)

• More than 4 weeks since prior and no concurrent major surgery (defined as requiring general anesthesia) and recovered

• More than 1 week since prior and no concurrent immunization with attenuated live vaccines

• No concurrent chronic, systemic treatment with corticosteroids or other immunosuppressive agents

• Topical or inhaled corticosteroids are allowed

• No concurrent prophylactic growth factors

• Concurrent bisphosphonate therapy allowed

Related Conditions & MeSH terms

• Prostate Cancer
• Prostatic Neoplasms

Intervention

Drug:
• carboplatin
AUC = 5 by Calvert's formula, day 1 of each 21 day cycle
• RAD 001
5 mg orally starting on Day 2 then continuous
• prednisone
5 mg orally twice a day starting on Day 1 then continuous

Other:
• laboratory biomarker analysis
Samples will be collected from archival tissue.
• pharmacological study
Samples will be collected Cycle 1, day 1, 2 & 8 and Cycle 2, Day 1 & 2

Locations

Country	Name	City	State
United States	Barbara Ann Karmanos Cancer Institute	Detroit	Michigan
United States	Northshore University Health System	Evanston	Illinois
United States	Weisberg Cancer Treatment Center	Farmington Hills	Michigan
United States	Cancer Institute of New Jersey	New Brunswick	New Jersey

Sponsors (2)

Lead Sponsor	Collaborator
Barbara Ann Karmanos Cancer Institute	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time to Progression (TTP)	Progression defined as at least a 20% increase in the sum of the longest diameter (LD) of target lesions taking as references the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions.	Up to 63 days while on treatment, then up 90 days thereafter. From date of registration to date of progressive disease.
Secondary	Number of Participants With Toxicity as Measured by NCI CTCAE v3.0 Criteria	Number of Participants with Grade 3/4 Toxicity as measured by NCI CTCAE v3.0 criteria	Day 1 of each cycle (every 21 days), through study completion, an average of 6 months
Secondary	PSA Response Rate	PSA response rate with response defined as => a 30% reduction in PSA	Day 1 of each cycle (every 21 days), through study completion, an average of 6 months
Secondary	Association of PSA Response Rate With Correlative Markers (Phospho mTOR, pAKT, and p70S6)	PSA response defined as a decrease of 30% or more will be tabled against mTOR, pAKT, and p70S6 (1+, 2+, 3+ vs ND)	Archival tissue will be collected if available. Optional biopsies pre-treatment and 24 hours after first everolimus and carboplatin dose
Secondary	Pharmacokinetics: Observed Carboplatin AUC Was Estimated Based on the Concentration in the 2.75-h Sample.	Using a limited sampling model (i.e., AUC = 0.52 × C2.75h + 0.92) (Sorensen et al., 1993), observed carboplatin AUC was estimated based on the concentration in the 2.75-h sample.	Samples were collected Cycle 2, Day 1
Secondary	Overall Survival	Overall Survival as measured by the Kaplan-Meier method	After treatment, participants will be contacted every 3 months up to 4 years

External Links

•   Clinical trial summary from the National Cancer Institute's PDQ® database