跳至主要内容
临床试验/NCT04921137
NCT04921137招募中4 期

A Randomised, Multicentre Trial Evaluating Harms and Benefits of Endocrine Therapy in Patients ≥70 Years of Age With Lower Risk Breast Cancer (REaCT-70)

Ottawa Hospital Research Institute15 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2021年8月19日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
招募中
入组人数
500
试验地点
15
主要终点
Accrual of 100 participants across 8 centres within 2 years

研究概览

简要总结

The current standard of care for stage 1 hormone receptor-positive (HR+) breast cancer consists of breast-conserving surgery followed by adjuvant radiotherapy (RT) and endocrine therapy (ET) for at least 5 years. The benefit of adjuvant ET for older patients is mitigated because of their increase risk of death from other causes and shorter time horizon to live. Clinical and pathological factors such as low-intermediate grade, tumor size ≤2 cm, and older age have been used in a few studies to identify patients with a lower risk of recurrence that might benefit from adjuvant therapy de-escalation, i.e. omission of RT or ET. Since there is no dedicated randomized clinical trial (RCT) conducted to evaluate the omission of ET, there is clinical equipoise as to whether we can omit adjuvant ET in older patients with lower-risk early-stage breast cancer. Therefore, we propose a randomised, multicentre trial evaluating harms and benefits of endocrine therapy in patients ≥70 years of age with lower risk breast cancer.

详细描述

The current standard of care for stage 1 hormone receptor-positive (HR+) breast cancer consists of breast-conserving surgery followed by adjuvant radiotherapy (RT) and endocrine therapy (ET) for at least 5 years. The benefit of adjuvant ET for older patients is mitigated because of their increase risk of death from other causes and shorter time horizon to live. This population is also more likely to have additional comorbidities which can lead to higher treatment-related adverse events impacting quality of life and precipitating functional decline. Clinical and pathological factors such as low-intermediate grade, tumor size ≤2 cm, and older age have been used in a few studies to identify patients with a lower risk of recurrence that might benefit from adjuvant therapy de-escalation, i.e. omission of RT or ET. The body of evidence from small prospective studies, mathematical modelling study and retrospective analyses would suggest that the omission of ET in older patients with favourable HR+ breast cancer who had optimal local therapy (i.e. breast conserving surgery followed by adjuvant radiotherapy) does not compromise locoregional and survival outcomes. Since there is no dedicated randomized clinical trial (RCT) conducted to evaluate the omission of ET, there is clinical equipoise as to whether we can omit adjuvant ET in older patients with lower-risk early-stage breast cancer. Therefore, we propose a randomised, multicentre trial evaluating harms and benefits of endocrine therapy in patients ≥70 years of age with lower risk breast cancer.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
70 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • New invasive estrogen and/or progesterone receptor-positive (ER+ and/or PR+), HER2-negative (HER2-) invasive breast carcinoma diagnosis as per ASCO-CAP guidelines
  • The primary tumour characteristics are either: Grade 1 and ≤3 cm on microscope exam, OR Grade 2 and ≤2 cm on microscope exam, OR Grade 3 and ≤1 cm on microscope exam
  • Treated with standard loco-regional therapy: breast conserving surgery followed by adjuvant radiotherapy OR total mastectomy
  • Axillary node-negative (cN0 or pN0)
  • Able to provide oral consent and complete questionnaires in French or English as per study protocol

排除标准

  • Metastatic cancer

研究组 & 干预措施

Omission of endocrine therapy

Experimental

Omission of endocrine therapy

干预措施: No endocrine therapy (Other)

Administration of endocrine therapy for at least 5 years

Active Comparator

Administration of endocrine therapy for at least 5 years

干预措施: Endocrine therapy (Other)

结局指标

主要结局

Accrual of 100 participants across 8 centres within 2 years

时间窗: 2 years after study initiation

The accrual of at least 100 participants at 8 centres within 2 years.

Participation rate of at least 60%

时间窗: 2 years after study initiation

A participation rate of at least 60% among participants approached.

90% treatment allocation rate

时间窗: 4 weeks after study enrolment

At least 90% of enrolled participants receive treatment as per their allocated intervention for at least 4 weeks

次要结局

  • Significant adverse events(Baseline, 12 weeks, 26 weeks, 1 year, 2 years, 3 years, 4 years and 5 years after study enrolment)
  • Health-related quality of life scores(Baseline, 12 weeks, 26 weeks, 1 year, 2 years, 3 years, 4 years and 5 years after study enrolment)
  • Rate of treatment discontinuation(5 years after study enrolment)
  • Endocrine therapy related toxicity(Baseline, 12 weeks, 26 weeks, 1 year, 2 years, 3 years, 4 years and 5 years after study enrolment)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (15)

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