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临床试验/NCT05914792
NCT05914792进行中(未招募)不适用

Longitudinal ctDNA Monitoring in Older Women With ER+ Breast Cancer Who Forego Upfront Surgery in Favor of Primary Endocrine Therapy

University of Pittsburgh1 个研究点 分布在 1 个国家目标入组 49 人开始时间: 2022年4月19日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
49
试验地点
1
主要终点
Proportion of ctDNA positivity

研究概览

简要总结

This prospective study recruits patients with ER+/HER2-, non-metastatic breast cancer who omit upfront surgery in favor of primary endocrine therapy for sample collection and prospective circulating tumor DNA (ctDNA) measurement to guide disease surveillance.

详细描述

Age is one of the most important risk factors for the development of breast cancer. Nearly a third of all breast cancer cases occur in older women (aged ≥ 70 years), with most cases being estrogen receptor-positive (ER+). Such tumours are unlikely to be the ultimate cause of death for older women, particularly when considering other comorbidities. Our group has recently shown that risk of breast cancer-related mortality is only around 3% for older women who forego upfront surgery and instead treated with primary endocrine monotherapy. However, with omission of surgery, surveillance for tumor growth or treatment failure is important but requires patients (and their caregivers) to have regular imaging and to see their oncology team every 3 months, which can be quite burdensome. Thus, this study employs a ctDNA surveillance scheme to monitor for potential tumor growth. Partnering with Natera, this study uses a bespoke, tumor-specific ctDNA assay (Signatera) to monitor for changes in ctDNA dynamics while the patient is on endocrine therapy.

This study is for patients who choose not to undergo primary surgical intervention and are managed medically on primary endocrine therapy (any endocrine therapy permitted). Patients will undergo Signatera testing at the time of regularly scheduled clinic follow-up visits and/or at the time of surveillance imaging, which will occur every 3-6 months. Patients will also be asked to complete regular surveys while participating in the study.

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
70 Years 至 —(Older Adult)
性别
Female
接受健康志愿者

入选标准

  • early-stage (stages I-III) breast cancer
  • estrogen receptor positive (ER+) and/or progesterone receptor positive (PR+) and HER2 receptor negative
  • able to provide blood samples
  • decision made by treating physician and patient to forego upfront surgery in favor of medical management with endocrine therapy
  • non-metastatic disease at diagnosis (patients need not have staging scans; patients at higher risk for de novo stage IV disease should not have any symptoms concerning for metastatic disease)
  • patients may be taking any endocrine therapy
  • patients may be taking any CDK4/6 inhibitor as deemed necessary by their treating physician
  • any ECOG Performance Status allowed
  • if patients have synchronous bilateral ER+ breast cancer, tissue from both sites should be submitted to Natera to perform ctDNA testing
  • patients with multifocal/multicentric tumors are eligible and the largest focus of cancer should be submitted for testing

排除标准

  • under 70 years of age
  • breast cancer that is not estrogen receptor positive (ER+) or progesterone receptor (PR+)
  • unable to provide blood samples or insufficient tumor tissue for Signatera testing

结局指标

主要结局

Proportion of ctDNA positivity

时间窗: Up to 5 years

Proportion of patients with ER+/HER2- breast cancer who omit upfront surgery in favor of primary endocrine therapy who have any ctDNA positivity using Signatera assay.

次要结局

  • Overall survival (OS)(Up to 5 years)
  • Breast cancer-specific survival (BCSS)(Up to 5 years)
  • Longitudinal quality of life assessment using National Comprehensive Cancer Network/Functional Assessment of Cancer Therapy Breast Cancer Symptom Index - 16 Item Version (NCCN NFBSI-16)(Up to 5 years)
  • Progression-free survival (PFS)(Up to 5 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Priscilla McAuliffe

Assistant Professor of Medicine

University of Pittsburgh

研究点 (1)

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