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

Primary Purpose

Breast Cancer

Status
Recruiting
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
No endocrine therapy
Endocrine therapy
Sponsored by
Ottawa Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring Radiation therapy, Endocrine therapy, Older patients, Adjuvant therapy

Eligibility Criteria

70 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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 ≤5 cm on microscope exam, OR Grade 2 and ≤3 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 lymph node-negative (N0)
  • Able to provide oral consent and complete questionnaires in French or English as per study protocol

Exclusion Criteria:

  • Metastatic cancer

Sites / Locations

  • The Ottawa HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Omission of endocrine therapy

Administration of endocrine therapy for at least 5 years

Arm Description

Omission of endocrine therapy

Administration of endocrine therapy for at least 5 years

Outcomes

Primary Outcome Measures

Accrual of 100 participants across 8 centres within 2 years
The accrual of at least 100 participants at 8 centres within 2 years.
Participation rate of at least 60%
A participation rate of at least 60% among participants approached.
90% treatment allocation rate
At least 90% of enrolled participants receive treatment as per their allocated intervention for at least 4 weeks

Secondary Outcome Measures

Significant adverse events
Significant adverse events (e.g. bone fracture, stroke/transient ischemic attack, thromboembolic event, cardiac event, second cancer, hospitalization and death)
Endocrine therapy related toxicity
Endocrine therapy (ET) related toxicity based upon Common Terminology for Adverse Events version 5 (CTCAEv5)
Health-related quality of life scores
Health-related quality of life (HR-QoL) scores measured by the Cancer and Aging Research Group geriatric assessment (patient-tool) and the Functional Assessment of Cancer Therapy - Endocrine Symptom Subscale (FACT-B plus ES). The Cancer and Aging Research Group geriatric assessment tool (patient-tool) is utilized to capture information about a patient's medical history as well as functional, cognitive and psychosocial status. The FACT-B plus ES is used to measure the side effects and putative benefits of hormonal treatment given in breast cancer.
Rate of treatment discontinuation
The rate of endocrine therapy treatment discontinuations and reasons why the endocrine therapy treatment was discontinued.

Full Information

First Posted
May 27, 2021
Last Updated
September 13, 2022
Sponsor
Ottawa Hospital Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT04921137
Brief Title
Evaluating Harms and Benefits of Endocrine Therapy in Patients ≥70 Years of Age With Lower Risk Breast Cancer
Official Title
A Randomised, Multicentre Trial Evaluating Harms and Benefits of Endocrine Therapy in Patients ≥70 Years of Age With Lower Risk Breast Cancer (REaCT-70)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 19, 2021 (Actual)
Primary Completion Date
September 2023 (Anticipated)
Study Completion Date
September 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ottawa Hospital Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
Radiation therapy, Endocrine therapy, Older patients, Adjuvant therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Omission of endocrine therapy
Arm Type
Experimental
Arm Description
Omission of endocrine therapy
Arm Title
Administration of endocrine therapy for at least 5 years
Arm Type
Active Comparator
Arm Description
Administration of endocrine therapy for at least 5 years
Intervention Type
Other
Intervention Name(s)
No endocrine therapy
Intervention Description
No endocrine therapy given
Intervention Type
Other
Intervention Name(s)
Endocrine therapy
Intervention Description
Endocrine therapy given for at least 5 years
Primary Outcome Measure Information:
Title
Accrual of 100 participants across 8 centres within 2 years
Description
The accrual of at least 100 participants at 8 centres within 2 years.
Time Frame
2 years after study initiation
Title
Participation rate of at least 60%
Description
A participation rate of at least 60% among participants approached.
Time Frame
2 years after study initiation
Title
90% treatment allocation rate
Description
At least 90% of enrolled participants receive treatment as per their allocated intervention for at least 4 weeks
Time Frame
4 weeks after study enrolment
Secondary Outcome Measure Information:
Title
Significant adverse events
Description
Significant adverse events (e.g. bone fracture, stroke/transient ischemic attack, thromboembolic event, cardiac event, second cancer, hospitalization and death)
Time Frame
Baseline, 12 weeks, 26 weeks, 1 year, 2 years, 3 years, 4 years and 5 years after study enrolment
Title
Endocrine therapy related toxicity
Description
Endocrine therapy (ET) related toxicity based upon Common Terminology for Adverse Events version 5 (CTCAEv5)
Time Frame
Baseline, 12 weeks, 26 weeks, 1 year, 2 years, 3 years, 4 years and 5 years after study enrolment
Title
Health-related quality of life scores
Description
Health-related quality of life (HR-QoL) scores measured by the Cancer and Aging Research Group geriatric assessment (patient-tool) and the Functional Assessment of Cancer Therapy - Endocrine Symptom Subscale (FACT-B plus ES). The Cancer and Aging Research Group geriatric assessment tool (patient-tool) is utilized to capture information about a patient's medical history as well as functional, cognitive and psychosocial status. The FACT-B plus ES is used to measure the side effects and putative benefits of hormonal treatment given in breast cancer.
Time Frame
Baseline, 12 weeks, 26 weeks, 1 year, 2 years, 3 years, 4 years and 5 years after study enrolment
Title
Rate of treatment discontinuation
Description
The rate of endocrine therapy treatment discontinuations and reasons why the endocrine therapy treatment was discontinued.
Time Frame
5 years after study enrolment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 ≤5 cm on microscope exam, OR Grade 2 and ≤3 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 lymph node-negative (N0) Able to provide oral consent and complete questionnaires in French or English as per study protocol Exclusion Criteria: Metastatic cancer
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lisa Vandermeer, MSc
Phone
613-737-7700
Ext
73039
Email
lvandermeer@toh.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Marta Sienkiewicz, MSc
Phone
613-737-7700
Email
msienkiewicz@ohri.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marie-France Savard, MD
Organizational Affiliation
Ottawa Hospital Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Ottawa Hospital
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H8L6
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marie-France Savard, MD
Phone
6137377700
Ext
70170
Email
msavard@toh.ca

12. IPD Sharing Statement

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

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