Impact of DNA Repair Pathway Alterations on Sensitivity to Radium-223 in Bone Metastatic Castration-resistant Prostate Cancer
About this study
This study investigates how well radium-223 works in treating patients with castration-resistant prostate cancer than has spread to the bones (bone metastases). Prostate cancer is the most common cancer in men and the second leading cause of cancer death. Furthermore, many men with notably advanced disease have been found to have abnormalities in DNA repair. The purpose of this research is to study the role of a DNA repair pathway in prostate cancer, specifically in response to administration of radium-223, an FDA-approved drug known to cause DNA damage to cancerous cells. Understanding how defects in the DNA repair pathway affects radium-223 treatment of prostate, may help doctors help plan effective treatment in future patients.
- Condition
- Castration-Resistant Prostate Carcinoma, Metastatic Malignant Neoplasm in the Bone, Metastatic Prostate Carcinoma, Stage IVB Prostate Cancer AJCC v8
- Tested
- Biospecimen Collection, Questionnaire Administration, Radium Ra 223 Dichloride
- Sponsor
- University of Washington
Who can join
- Age
- 18 years and older
- Sex
- Male only
- Healthy volunteers
- Not accepted
Inclusion 14
- Minimum age: 18 years
- Eligible sex: Male
- Study condition: Castration-Resistant Prostate Carcinoma, Metastatic Malignant Neoplasm in the Bone, Metastatic Prostate Carcinoma, Stage IVB Prostate Cancer AJCC v8
- Patient must be \>= 18 years of age
- Patient must have histopathologic diagnosis of prostate cancer
- Patient must have castration-resistant prostate cancer
- Patient must have radiographic evidence of bone metastasis
- Patients must be symptomatic from prostate cancer
- Patient must have plans to undergo treatment with radium-223
- Patient must have a PSA level \>= 10 ng/mL
- Patient must have castrate testosterone levels demonstrated within the last 3 months prior to screening
- Patient must have anticipated survival \> 3 months
- Patient must be willing and able to authorize consent
- Patient must be willing and able to comply with the protocol, including follow-up visits
Exclusion 9
- Patient must not have visceral metastasis
- Patients on regimens of radium-223 in combination with other antineoplastic agents are excluded
- \* Bone-targeted only therapy (e.g. denosumab or zoledronic acid) will be allowed
- Patients who have received prior radium-223
- Patients who have received prior platinum containing chemotherapy
- Absolute neutrophil count (ANC) \< 1.5 x 10\^9/L
- Hemoglobin (HB) \< 9 g/dL
- Platelets (PLT) \< 100 x 10\^9/L
- Any condition which, in the investigator's opinion, makes the subject unsuitable for trial participation
Where
4 sites, 3 recruiting
Johns Hopkins University
Baltimore, Maryland, United States
University of Wisconsin-Madison
Madison, Wisconsin, United States
Fred Hutch/University of Washington Cancer Consortium
Seattle, Washington, United States
Bozeman Health Deaconess Hospital
Bozeman, Montana, United States
Contact
-
Jane Romani
206-606-1909 jromani@fredhutch.org
Potential match only. Final eligibility is determined by the study team.