An Open-label Phase II Study With SUTENT in Patients Suffering From Hormone Refractory Prostate Cancer (PROSUT)

Assistance Publique - Hôpitaux de Paris

Status and phase

Completed

Phase 2

Conditions

Neoplasms, Hormone-Dependent

Tumor Markers, Biological

Prostatic Neoplasms

Disease-Free Survival

Survival Rate

Treatments

Drug: sunitinib

Study type

Interventional

Funder types

Other

Identifiers

NCT00748358

P070404

Details and patient eligibility

About

as second-line treatment in metastatic prostate cancer, the present study will investigate the efficacy of sunitinib (SUTENT) given orally at a dose of 37.5 mg continuously, for 6 cycles of 6 consecutive weeks .Patients who are still responders after 6 cycles will be treated until disease progression, pain progression, unacceptable toxicity or death due to any cause.

Dose increase or reduction of 12.5 mg increments and change of schedule is recommended based on individual safety and tolerability.

Follow-up for up to 1 year from the last dose of sunitinib.

Full description

Antitumor efficacy of sunitinib will be assessed as follows:
- PSA response rate and PSA progression according Working Group Criteria,
- Variation of PSA doubling time (PSADT) before and after initiation of the treatment,
- Objective response rate (ORR) according to RECIST criteria,
- Clinical benefit,
- Overall survival (OS).
Pharmacokinetic endpoints will include sunitinib and its metabolite, SU012662, plasma levels and estimation of the population pharmacokinetic parameters as well as the inter-individual variability of these parameters, for a subgroup of 30 patients.
The biological effects of sunitinib in patients with metastatic prostate carcinoma will be evaluated by measurements of the different biological markers that could be modulated by this antiangiogenic therapeutic, and could then predict and monitor disease progression and response to treatment:
- Bone tumor markers: bone resorption markers (uCTX, uCTX, ICTP, CTX-MMP and TRACP-5b), bone formation markers (OC, PINP and BALP), osteoclastogenesis markers (OPG and RANKL) and parameters as calcium, phosphate, creatinine, albumin, PTH and 25(OH)D.
- Angiogenesis markers: bFGF, SDF-1, VEGF-A, VEGFR1 and VEGFR2, CECs and CEPs, endothelial and platelet microparticles.

Enrollment

50 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Signed and dated IRB/EC-approved informed consent
Age 18 years or older
Histologically confirmed prostate adenocarcinoma
Metastatic HRPC
Received prior castration by orchidectomy and/or LH-RH agonist with or without antiandrogen, antiandrogen withdrawal, monotherapy with estramustine, or other hormonal agents.
Tumor disease must be progressive after a first line using docetaxel based chemotherapy, eventually in association with estramustine. Docetaxel based regimen may have been interrupted and restarted. Patient must have either measurable (RECIST criteria) or non-measurable (bone) disease and/or clinical progression (bone pain) and/or biological progression (PSA Working Group criteria).
Discontinuation from previous chemotherapy and/or radiation therapy at least 4 weeks prior to treatment initiation
Performance status of 0 to 2 on the Eastern Cooperative Oncology Group (ECOG) scale
Patient of child bearing potential must use effective contraception. Female partners of treated patients with child bearing potential must use oral contraceptives or intra uterine device (IUD)
Life expectancy of at least 3 months
Resolution of all acute toxic effects of any prior local treatment to NCI CTCAE grade 1
Patients must have adequate organ functions defined
Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures
Patient covered by the National Health System

Exclusion criteria

Prior treatment with sunitinib or other antiangiogenic agent
More than 1 line of chemotherapy
External beam radiotherapy for ≥ 50% of bone marrow
Uncontrolled hypertension (systolic blood pressure > 150 mm Hg or diastolic blood pressure > 90 mm Hg despite optimal medical management)
Any of the following within 12 months prior to treatment initiation: severe/unstable angina, myocardial infarction, coronary artery bypass graft, symptomatic congestive heart failure, thrombotic or embolic events such as cerebrovascular accident including transient ischemic attack
Ongoing cardiac dysrhythmias of grade 2, atrial fibrillation of any grade
Treatment with anticonvulsant agents and treatment with therapeutic doses of coumarin-derivative anticoagulants such as warfarin currently or within 2 weeks prior to first day of Sunitinib administration. Low dose of warfarin for deep vein thrombosis prophylaxis is permitted (up to 2 mg/day) and low molecular weight heparin is allowed
Any medical condition that might interfere with oral medication absorption
Known or suspected brain metastasis, or carcinomatous meningitis, or spinal cord compression
Diagnosis of any second malignancy within the last 3 years, with the exception of treated basal cell or squamous cell carcinoma and pT1/a bladder cancer with no evidence of recurrent disease for 12 months
Any acute or chronic medical or psychiatric disorder incompatible with the study
Known human immunodeficiency virus or acquired immunodeficiency syndrome-related illness
Treatment with others investigational drugs or participation in another clinical trial within the past 4 weeks, or concomitantly with this trial