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Partial Breast Re-irradiation Using Ultra Hypofractionation (PRESERVE) (PRESERVE)

Primary Purpose

Breast Cancer, Breast Cancer Recurrent

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
rPBI
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring Hypofractionated

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > 18 years
  • In-breast recurrence confirmed as unicentric
  • Tumour <3.0 cm in greatest diameter on pathologic examination, including both invasive and non-invasive components
  • >1 year after completion of prior adjuvant whole or partial breast radiotherapy
  • Clinically node negative
  • Negative margins (no tumour on ink)
  • Recovered from surgery with the incision completely healed and no signs of infection
  • Negative metastatic work-up (no evidence of distant metastases on bone scan, and computerized tomography (CT) scans of the thorax, abdomen, and pelvis; or using (FDG) Positron emission tomography (PET)-CT).

Exclusion Criteria:

  • Infiltrating Lobular Carcinoma
  • Multifocal or multicentric disease
  • Extensive intraductal component
  • T4 disease
  • Node positive or distant metastatic disease
  • Serious non-malignant disease (cardiovascular, pulmonary, systemic lupus erythematosus, scleroderma), which would preclude radiation treatment
  • Currently pregnant or lactating
  • Presence of an ipsilateral breast implant or pacemaker
  • Unable to commence radiation within 16 weeks of breast-conserving surgery (or last surgical procedure on the breast) or within 12 weeks from last cycle of adjuvant chemotherapy
  • Unable to clearly define the surgical cavity (Level I oncoplastic procedures are permitted provided the tumor bed is well delineated with surgical clips).
  • Psychiatric disorders which would preclude obtaining informed consent or adherence to protocol
  • Grade II or more late skin toxicity from prior radiation evaluated and graded using CTCAE v5.0

Sites / Locations

  • Princess Margaret Cancer CentreRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

rPBI

Arm Description

26Gy in 5 daily fractions over 1-week

Outcomes

Primary Outcome Measures

Number of participants accrued to the trial
The primary endpoint will be determined by the ability to complete accrual of 15 patients to the study in 2 years.

Secondary Outcome Measures

Frequency radiation-associated toxicity (acute)
Radiation-associated toxicities (acute) will be graded according to CTCAE v5.0 by physicians. Toxicity associated with treatment will be summarized using frequency with 95% Clopper-Pearson confidence intervals by grade at each scheduled follow up.
Percentage radiation-associated toxicity (acute)
Radiation-associated toxicities (acute) will be graded according to CTCAE v5.0 by physicians. Toxicity associated with treatment will be summarized using percentage with 95% Clopper-Pearson confidence intervals by grade at each scheduled follow up.
Frequency radiation-associated toxicity (late)
Radiation-associated toxicities (late) will be graded according to CTCAE v5.0 by physicians. Toxicity associated with treatment will be summarized using frequency with 95% Clopper-Pearson confidence intervals by grade at each scheduled follow up.
Percentage radiation-associated toxicity (late)
Radiation-associated toxicities (late) will be graded according to CTCAE v5.0 by physicians. Toxicity associated with treatment will be summarized using percentage with 95% Clopper-Pearson confidence intervals by grade at each scheduled follow up.
Risk of local recurrence (invasive and DCIS)
Cumulative incidence function will be used to estimate local recurrence with death as a competing risk.
Risk of distant recurrence (invasive and DCIS)
Cumulative incidence function will be used to estimate distant recurrence and distance recurrence with death as a competing risk.
Location of local recurrence (in-field) (frequency)
Location of recurrence will be summarized by frequency.
Location of local recurrence (in-field) (percentage)
Location of recurrence will be summarized by percentage.
Location of local recurrence (out-of-field) (frequency)
Location of recurrence will be summarized by frequency.
Location of local recurrence (out-of-field) (percentage)
Location of recurrence will be summarized by percentage
Risk of local recurrence after rPBI requiring mastectomy
Cumulative incidence function will be used to estimate local recurrence after rPBI requiring mastectomy with death as a competing risk
Invasive breast cancer free survival
Kaplan-Meier method will be used to estimate invasive breast cancer free survival
Overall survival
Kaplan-Meier method will be used to estimate overall survival

Full Information

First Posted
October 14, 2022
Last Updated
June 27, 2023
Sponsor
University Health Network, Toronto
Collaborators
Sunnybrook Health Sciences Centre, Royal Victoria Regional Health Centre, AC Camargo Cancer Center, King Hussein Cancer Center, Tata Memorial Hospital, NYU Langone Health, Centre hospitalier de l'Université de Montréal (CHUM), Peter MacCallum Cancer Centre, Australia
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1. Study Identification

Unique Protocol Identification Number
NCT05592938
Brief Title
Partial Breast Re-irradiation Using Ultra Hypofractionation (PRESERVE)
Acronym
PRESERVE
Official Title
Partial Breast Re-irradiation Using Ultra Hypofractionation: Phase 2 Multi-institutional Study (PRESERVE)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 27, 2023 (Actual)
Primary Completion Date
June 27, 2027 (Anticipated)
Study Completion Date
June 27, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
Collaborators
Sunnybrook Health Sciences Centre, Royal Victoria Regional Health Centre, AC Camargo Cancer Center, King Hussein Cancer Center, Tata Memorial Hospital, NYU Langone Health, Centre hospitalier de l'Université de Montréal (CHUM), Peter MacCallum Cancer Centre, Australia

4. Oversight

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

5. Study Description

Brief Summary
Breast-conserving surgery followed by re-irradiation with partial breast irradiation (rPBI) has recently been found to be a safe alternative to mastectomy for women who have undergone prior whole breast radiation. By reducing the volume of tissue receiving radiation, rPBI has been associated with less toxicity and improved cosmetic outcomes. For many women with early stage breast cancer, shorter 1-week (5-fraction) courses of breast radiation (ultra-fractionation) have been found to be equivalent to longer fractionation schedules in the upfront treatment setting. These 1-week schedules are more convenient for patients, with fewer treatments and shorter overall treatment time. The investigators hypothesize that they can accrue sufficient patient with rPBI who will be treated using 26 Gray(Gy) in 5 daily fractions over 1-week. Planned interim analysis after the 15 recruited patients for early toxicity evaluation with stopping rule for unacceptable toxicity.
Detailed Description
Breast cancer is the leading cause of cancer in women worldwide, with over 2 million cases diagnosed every year. Although advances in treatment have led to an overall reduction in breast cancer mortality, survivors continue to have an ongoing risk of disease recurrence. For women who experience breast recurrence, mastectomy has historically been the only treatment approach offered. However, it has been associated with negative health outcomes, including reduced quality of life, depression and anxiety, and impaired sexual functioning. Fear of mastectomy has also been associated with delays in seeking appropriate and timely management of disease. As a result, there is increasing interest to identify treatment options that include breast preservation. Breast-conserving surgery followed by re-irradiation with partial breast irradiation (rPBI) has recently been found to be a safe alternative to mastectomy for women who have undergone prior whole breast radiation. By reducing the volume of tissue receiving radiation, rPBI has been associated with less toxicity and improved cosmetic outcomes. However, previously published studies have used long fractionation regimens for rPBI delivered over 3 to 5 weeks, which can present a challenge for both patients and health systems. This is particularly true in low- and middle-income countries, where more than half of new breast cancer cases now occur. For many women with early stage breast cancer, shorter 1-week (5-fraction) courses of breast radiation (ultra-fractionation) have been found to be equivalent to longer fractionation schedules in the upfront treatment setting. These 1-week schedules are more convenient for patients, with fewer treatments and shorter overall treatment time. The investigators hypothesize that they can accrue sufficient patient with rPBI who will be treated using 26Gy in 5 daily fractions over 1-week. Planned interim analysis after the 15 recruited patients for early toxicity evaluation with stopping rule for unacceptable toxicity. Using an international network of comprehensive cancer centers, this study will advance global knowledge of how to optimally treat woman with this disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Breast Cancer Recurrent
Keywords
Hypofractionated

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
rPBI
Arm Type
Experimental
Arm Description
26Gy in 5 daily fractions over 1-week
Intervention Type
Radiation
Intervention Name(s)
rPBI
Intervention Description
External beam partial breast reirradiation (rPBI) using 26Gy in 5 fractions delivered daily over 1-week
Primary Outcome Measure Information:
Title
Number of participants accrued to the trial
Description
The primary endpoint will be determined by the ability to complete accrual of 15 patients to the study in 2 years.
Time Frame
During accrual period, up to 2 years
Secondary Outcome Measure Information:
Title
Frequency radiation-associated toxicity (acute)
Description
Radiation-associated toxicities (acute) will be graded according to CTCAE v5.0 by physicians. Toxicity associated with treatment will be summarized using frequency with 95% Clopper-Pearson confidence intervals by grade at each scheduled follow up.
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Percentage radiation-associated toxicity (acute)
Description
Radiation-associated toxicities (acute) will be graded according to CTCAE v5.0 by physicians. Toxicity associated with treatment will be summarized using percentage with 95% Clopper-Pearson confidence intervals by grade at each scheduled follow up.
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Frequency radiation-associated toxicity (late)
Description
Radiation-associated toxicities (late) will be graded according to CTCAE v5.0 by physicians. Toxicity associated with treatment will be summarized using frequency with 95% Clopper-Pearson confidence intervals by grade at each scheduled follow up.
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Percentage radiation-associated toxicity (late)
Description
Radiation-associated toxicities (late) will be graded according to CTCAE v5.0 by physicians. Toxicity associated with treatment will be summarized using percentage with 95% Clopper-Pearson confidence intervals by grade at each scheduled follow up.
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Risk of local recurrence (invasive and DCIS)
Description
Cumulative incidence function will be used to estimate local recurrence with death as a competing risk.
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Risk of distant recurrence (invasive and DCIS)
Description
Cumulative incidence function will be used to estimate distant recurrence and distance recurrence with death as a competing risk.
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Location of local recurrence (in-field) (frequency)
Description
Location of recurrence will be summarized by frequency.
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Location of local recurrence (in-field) (percentage)
Description
Location of recurrence will be summarized by percentage.
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Location of local recurrence (out-of-field) (frequency)
Description
Location of recurrence will be summarized by frequency.
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Location of local recurrence (out-of-field) (percentage)
Description
Location of recurrence will be summarized by percentage
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Risk of local recurrence after rPBI requiring mastectomy
Description
Cumulative incidence function will be used to estimate local recurrence after rPBI requiring mastectomy with death as a competing risk
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Invasive breast cancer free survival
Description
Kaplan-Meier method will be used to estimate invasive breast cancer free survival
Time Frame
3 months, 1 year, and 3 years post rPBI
Title
Overall survival
Description
Kaplan-Meier method will be used to estimate overall survival
Time Frame
3 months, 1 year, and 3 years post rPBI

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years In-breast recurrence confirmed as unicentric Tumour <3.0 cm in greatest diameter on pathologic examination, including both invasive and non-invasive components >1 year after completion of prior adjuvant whole or partial breast radiotherapy Clinically node negative Negative margins (no tumour on ink) Recovered from surgery with the incision completely healed and no signs of infection Negative metastatic work-up (no evidence of distant metastases on bone scan, and computerized tomography (CT) scans of the thorax, abdomen, and pelvis; or using (FDG) Positron emission tomography (PET)-CT). Exclusion Criteria: Infiltrating Lobular Carcinoma Multifocal or multicentric disease Extensive intraductal component T4 disease Node positive or distant metastatic disease Serious non-malignant disease (cardiovascular, pulmonary, systemic lupus erythematosus, scleroderma), which would preclude radiation treatment Currently pregnant or lactating Presence of an ipsilateral breast implant or pacemaker Unable to commence radiation within 16 weeks of breast-conserving surgery (or last surgical procedure on the breast) or within 12 weeks from last cycle of adjuvant chemotherapy Unable to clearly define the surgical cavity (Level I oncoplastic procedures are permitted provided the tumor bed is well delineated with surgical clips). Psychiatric disorders which would preclude obtaining informed consent or adherence to protocol Grade II or more late skin toxicity from prior radiation evaluated and graded using CTCAE v5.0
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Danielle Rodin, MD
Phone
(416) 946-6513
Email
danielle.rodin@rmp.uhn.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Anne Koch, MD
Phone
(416) 946-2919
Email
anne.koch@rmp.uhn.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Danielle Rodin, MD
Organizational Affiliation
Princess Margaret Cancer Centre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anne Koch, MD
Organizational Affiliation
Princess Margaret Cancer Centre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Fadwa Abdel-Rahman, MBBS
Organizational Affiliation
Princess Margaret Cancer Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Princess Margaret Cancer Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G2C4
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne Koch, MD

12. IPD Sharing Statement

Plan to Share IPD
No
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Partial Breast Re-irradiation Using Ultra Hypofractionation (PRESERVE)

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