SIMCAP (Surgery in Metastatic Carcinoma of Prostate): Phase 2.5 Multi-Institution Randomized Prospective Clinical Trial Evaluating the Impact of Cytoreductive Radical Prostatectomy Combined With Best Systemic Therapy on Oncologic and Quality of Life Outcomes in Men With Newly Diagnosed Metastatic Prostate Cancer

Who is this study for? Adult patients with metastatic prostate cancer
Status: Recruiting
Location: See all (17) locations...
Intervention Type: Drug, Procedure, Other
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This randomized phase II trial studies how well surgical removal of the prostate and antiandrogen therapy with or without docetaxel work in treating men with newly diagnosed prostate cancer that has spread to other places in the body. Androgens can cause the growth of prostate cancer cells. Antiandrogen therapy may lessen the amount of androgens made by the body. Drugs used in chemotherapy, such as docetaxel work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Surgery, antiandrogen therapy and docetaxel may work better in treating participants with prostate cancer.

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: f
View:

• Histologically proven adenocarcinoma of the prostate

• Evidence of metastasis by magnetic resonance imaging (MRI)/computed tomography (CT) scan, bone scan, or histologic confirmation

• Clinical stage M1a (distant lymph node positive), M1b (bone metastasis), or M1c (solid organ metastasis.

• If solitary lesion, metastasis confirmed with either biopsy or two independent imaging modalities (i.e. CT and PET \[positron emission tomography\], bone scan and MRI, modality at the discretion of the treating physician)

• No previous local therapy for prostate cancer (i.e prostate radiation, cryotherapy, etc.)

• Give informed consent

• Prostate deemed resectable by surgeon

• Plans to start or has already started antiandrogen therapy (ADT) no longer than 6 months prior to consent

• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

• Hemoglobin (HgB) \>= 9 g/dL compatible for surgery

• Platelets \> 80,000/mcL compatible for surgery

• Aspartate aminotransferase (AST) =\< 2x upper limit of normal (ULN) compatible for surgery

• Alanine aminotransferase (ALT) =\< 2x upper limit of normal (ULN) compatible for surgery

Locations
United States
California
City of Hope
RECRUITING
Duarte
University of California, Irvine
TERMINATED
Irvine
University of Southern California
RECRUITING
Los Angeles
Connecticut
Yale University
RECRUITING
New Haven
New Jersey
Rutgers Cancer Institute of New Jersey
RECRUITING
New Brunswick
Pennsylvania
Unniversity of Pennsylvania
TERMINATED
Philadelphia
Washington
Swedish Medical Services
RECRUITING
Seattle
Other Locations
Australia
Epworth Healthcare
TERMINATED
East Melbourne
China
Chinese University of Hong Kong
RECRUITING
Hong Kong
Japan
Akita University
RECRUITING
Akita
Kindai University
RECRUITING
Ōsaka-sayama
Kyoto University
WITHDRAWN
Sako
Juntendo University
RECRUITING
Tokyo
Republic of Korea
National Cancer Center
RECRUITING
Goyang-si
Seoul National University Bundang Hospital
RECRUITING
Gyeonggi-do
Samsung Medical Center
RECRUITING
Seoul
Taiwan
National Taiwan University Hospital
RECRUITING
Taipei
Contact Information
Primary
Stephanie Ladd
ycciprojectmanagement@yale.edu
(203) 785-3482
Time Frame
Start Date: 2018-03-20
Estimated Completion Date: 2027-03
Participants
Target number of participants: 190
Treatments
Experimental: Arm I (ADT, docetaxel)
Participants receive antiandrogen therapy with or without docetaxel at the discretion of the treating physician.
Experimental: Arm II (ADT, radical prostatectomy, docetaxel)
Participants receive antiandrogen therapy for at least 1 month, then undergo cytoreductive radical prostatectomy. Participants continue antiandrogen therapy and may receive docetaxel prior to surgery at the discretion of the treating physician.
Related Therapeutic Areas
Sponsors
Leads: Yale University
Collaborators: National Cancer Institute (NCI)

This content was sourced from clinicaltrials.gov