跳至主要内容
临床试验/NCT04489719
NCT04489719
招募中
不适用

The Impact of DNA Repair Pathway Alterations Identified by Circulating Tumor DNA on Sensitivity to Radium-223 in Bone Metastatic Castration-Resistant Prostate Cancer

University of Washington4 个研究点 分布在 1 个国家目标入组 48 人2021年4月16日

概览

阶段
不适用
干预措施
Biospecimen Collection
疾病 / 适应症
Castration-Resistant Prostate Carcinoma
发起方
University of Washington
入组人数
48
试验地点
4
主要终点
Response rate
状态
招募中
最后更新
2个月前

概览

简要总结

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.

详细描述

OUTLINE: Patients receive standard of care radium Ra 223 dichloride given by intravenous (IV) bolus every 4 weeks for up to 6 cycles. Patients undergo collection of blood every 1-3 months during radium Ra 223 dichloride treatment. After completion of study, patients are followed up every 3 months for up to 5 years from the date of treatment completion.

注册库
clinicaltrials.gov
开始日期
2021年4月16日
结束日期
2029年8月1日
最后更新
2个月前
研究类型
Observational
性别
Male

研究者

责任方
Sponsor

入排标准

入选标准

  • 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

排除标准

  • 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

研究组 & 干预措施

Observational (biospecimen collection)

Patients receive standard of care radium Ra 223 dichloride given by IV bolus every 4 weeks for up to 6 cycles. Patients undergo collection of blood every 1-3 months during radium Ra 223 dichloride treatment.

干预措施: Biospecimen Collection

Observational (biospecimen collection)

Patients receive standard of care radium Ra 223 dichloride given by IV bolus every 4 weeks for up to 6 cycles. Patients undergo collection of blood every 1-3 months during radium Ra 223 dichloride treatment.

干预措施: Questionnaire Administration

Observational (biospecimen collection)

Patients receive standard of care radium Ra 223 dichloride given by IV bolus every 4 weeks for up to 6 cycles. Patients undergo collection of blood every 1-3 months during radium Ra 223 dichloride treatment.

干预措施: Radium Ra 223 Dichloride

结局指标

主要结局

Response rate

时间窗: Up to 1 year

Response will be defined as having one or both of the following: confirmed prostate specific antigen (PSA) decline of \>= 30% from baseline AND/OR confirmed alkaline phosphatase (ALP) decline \>= 30% from baseline. Response is evaluated throughout the course of treatment until the post-radium-223 end of treatment laboratory studies. Confirmation of response by PSA and/or ALP requires a second consecutive value obtained \>= 2 weeks after the first with sustained \>= 30% decline. Characterization of response rate to radium-223 in the DRD patient population will be assessed by binomial proportion with Clopper-Pearson exact 2-sided 95% confidence intervals.

次要结局

  • Response rate in those with previous PARP inhibitor therapy(Up to 1 year)
  • Number of radium Ra 223 dichloride(Up to 6 months)
  • Analgesic usage(Up to 1 year)
  • Quality of life (FACT-P survey)(Up to 1 year)
  • Overall survival(Up to 5 years)
  • Pain assessment(Up to 1 year)
  • Incidence of adverse events(Up to 1 year)
  • Response rate(Up to 1 year)

研究点 (4)

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