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临床试验/NCT02564120
NCT02564120已完成不适用

North Carolina Prostate Cancer Comparative Effectiveness & Survivorship Study (NC ProCESS)

UNC Lineberger Comprehensive Cancer Center1 个研究点 分布在 1 个国家目标入组 1,556 人开始时间: 2011年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,556
试验地点
1
主要终点
Prostate Cancer Recurrence

研究概览

简要总结

NC ProCESS is a cohort of patients from diverse backgrounds diagnosed with early prostate cancer, who were enrolled from January 2011-June 2013. These patients were recruited throughout North Carolina, and also in partnership with institutions across the country. Patients enrolled before they start treatment, and are then followed prospectively through treatment and then afterwards. This observational study collects information on quality of life, cancer control, and health care received inclusive of treatment and management of subsequent effects including complications and recurrence. The objective of this study is to examine comparative outcomes among different modern prostate cancer treatment options in this cohort of patients.

详细描述

Localized prostate cancer treatment options is consistently a "highest priority" comparative effectiveness research (CER) topic according to the Institute of Medicine, Agency for Healthcare Research and Quality (AHRQ), and other summary reports. Patients urgently need information on the comparative outcomes of modern treatment options to guide decision-making for this disease that causes significant burden based on its high prevalence, mortality and treatment effects on quality of life. The status quo as it pertains to prostate cancer is significant overtreatment causing potential patient harm, rapid diffusion of new/expensive technologies without proven benefit and patients lacking high quality research evidence to balance direct-to-consumer advertising and guide individualized decision-making.

NC ProCESS is a population-based cohort designed specifically to address well-described knowledge gaps. It was designed in close collaboration with the unique AHRQ consortium stakeholder group, which included representatives from patients, clinicians and policymakers. Stakeholders helped define study design to emphasize "real-world" patients and select patient-centered and relevant outcomes, and have been involved throughout assembly of this patient cohort. The diverse cohort is well-represented by "hard to reach" patients; enrollment before treatment avoids biases with participation and recall. As clinical trials are not feasible to address the central questions in prostate cancer CER, this prospective study will yield the highest level of evidence to inform patients and other stakeholders. With an assembled cohort, this study is necessary to examine comparative outcomes.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
35 Years 至 80 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Newly-diagnosed, histologically-proven, localized prostate adenocarcinoma.
  • Completion of baseline interview prior to initiating therapy.
  • Patient ability to complete study interview: no cognitive impairment, language or hearing problems.
  • Not diagnosed with prostate cancer through transurethral resection of the prostate (TURP).
  • English speaking.
  • Has telephone.

排除标准

  • Initiation of treatment for prostate cancer prior to completion of baseline interview.
  • Cognitive impairment.
  • Hearing problems.
  • Inability to speak or understand English.

结局指标

主要结局

Prostate Cancer Recurrence

时间窗: From date of completion of treatment (radiation or surgery) until the date of recurrence or date of death from any cause, whichever came first, assessed up to 5 years.

Percentage of patients who had a recurrence of prostate cancer during 5 years of follow-up.

Cancer-specific Quality of Life

时间窗: 4 years

Prostate Cancer Symptom Indices (PCSI) - measures treatment-related morbidity and adverse effects and is comprised of 4 functional scales measuring Sexual Dysfunction, Bowel Problems, Urinary Incontinence, and Urinary Obstruction/Irritation. Four parallel distress indices measure distress from symptoms. In each index, patient answers are converted to a score from 0 (no symptom/distress) to 100 (maximum symptoms/distress). A 5-10 point difference in QOL is considered "clinically meaningful."

Overall Quality of Life

时间窗: 4 years

Short Form-12 (SF12) - Measures health-related quality of life. Consists of Likert response formats that assess overall health, mental health, vitality, social functioning, and whether ones health or pain limits their daily physical activities. The SF-12 also contains four categorical questions (yes or no) that assess limitations in functioning due to physical and emotional health. The SF-12 provides the Mental Component Summary score (MCS) and Physical Component Summary score (PCS), calculated using norm-based scoring, with the mean set at 50 and standard deviation 10. A lower score indicates lower QOL.

次要结局

  • Decisional Regret(4 years)
  • 5-year Mortality(From date of diagnosis until date of death or end of follow-up up to 5 years)
  • Prostate Cancer Anxiety(4 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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