Evaluating Harms and Benefits of Endocrine Therapy in Patients ≥70 Years of Age With Lower Risk Breast Cancer

ConditionBreast Cancer
Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age70+
SponsorOttawa Hospital Research Institute

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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)

Disqualifiers

Metastatic cancer

Trial design

Design model

Parallel

Treatments tested in this trial

  • No endocrine therapy

    Other intervention

    No endocrine therapy given

  • Endocrine therapy

    Other intervention

    Endocrine therapy given for at least 5 years

Treatment groups

500 Participants
are divided into 2 treatment groups
Group A: Omission of endocrine therapyExperimental treatment 1 intervention
Group B: Administration of endocrine therapy for at least 5 yearsActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Hierarchical composite endpoint (OS, iDFS, MDFS, QoL)

The primary outcome is a hierarchical composite endpoint following the WIN-ratio approach. This composite endpoint includes overall survival (OS), invasive disease free survival (iDFS), metastatic disease free survival (MDFS), quality of life (QoL), joint pain, and hot flashes.

Time frame
5 years

Secondary outcomes

1

Overall survival

Overall survival (OS) is the time from the date of surgery to the date of death due to any cause.

Time frame
5 years
2

Invasive disease free survival

Invasive disease free suvival (iDFS) is the time from the surgery until the first occurrence of invasive ipsilateral, loco-regional, contralateral and distant breast tumor recurrence or death due to any cause

Time frame
5 years
3

Metastatic disease free survival

Metastatic disease free survival (MDFS) is the time from the surgery until the first occurrence of distant breast tumor recurrence of death due to any causes

Time frame
5 years
4

Health-related quality of life: FACT-B plus ES

Health-related quality of life is measured using the Functional Assessment of Cancer Therapy - Breast (FACT-B) plus the Functional Assessment of Cancer Therapy - Endocrine Symptoms (FACT-ES). The FACT-B has a total score of 0 to 148. FACT-ES has a total score of 0 to 184. Higher scores indicate better quality of life.

Time frame
Baseline, 26-weeks, 1-year, 2-years, 3-years, 4-years, 5-years

Other outcomes

Sponsors and contacts

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