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NCT05592938NARecruiting

Partial Breast Re-irradiation Using Ultra Hypofractionation (PRESERVE)

University Health Network, Toronto

Start Date

6/27/2023

Completion Date

6/27/2027

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 a 1-week ultra-hypofractionated rPBI regimen following breast-conserving surgery (BCS) for local recurrence or new primary breast cancer in the previously irradiated breast (LR) will be associated with acceptable toxicity at 1 year (\<13% grade \>3 toxicity).

Detailed Description

Most women affected by breast cancer are treated with breast-conserving surgery to remove the tumour, followed by radiation to reduce the risk of recurrence. Unfortunately, some women will experience recurrence of the cancer in the previously treated breast. These recurrences have historically been treated by removing the whole breast or a second breast-conserving surgery followed by 3 to 5 weeks of radiation. These treatments can negatively impact mental health and quality of life or lead to harmful side effects that could impact the skin, breast, ribs, heart and lungs. 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 a 1-week ultra-hypofractionated rPBI regimen following breast-conserving surgery (BCS) for local recurrence or new primary breast cancer in the previously irradiated breast (LR) will be associated with acceptable toxicity at 1 year (\<13% grade \>3 toxicity). The target population for this study is women with localized recurrent or new primary breast cancer in the previously irradiated breast. This is a prospective single arm phase 2 trial of external beam rPBI using 26Gy in 5 fractions delivered daily over 1-week after a second lumpectomy for LR following prior BCS and adjuvant whole or partial breast irradiation. Using a multi-institutional and international network of comprehensive cancer centers, this study will advance global knowledge of how to optimally treat women with this disease.

Eligibility Criteria

Age Range: 18 years to 99 years

Inclusion Criteria: * Age \> 18 years * In-breast recurrence or new primary (ductal carcinoma in situ (DCIS) or invasive carcinoma) * Tumour \<3.0 cm in greatest diameter on pathologic examination, including both invasive and non-invasive components * \>5 years after completion of prior adjuvant whole or partial breast radiotherapy (prior nodal radiotherapy permitted) * Clinically node negative * Negative margins (no tumour on ink) * Recovered from surgery with the incision completely healed and no signs of infection Exclusion Criteria: * Multicentric disease (patients with multifocal breast cancer in the same quadrant are eligible) * Tumour histology limited to lobular carcinoma only * 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 (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

Interventions

RADIATION

rPBI

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Conditions

Breast CancerBreast Cancer Recurrent

Locations

NYU Langone Health

New York, New York 10016

United States

Columbia University Medical Center

New York, New York 10032

United States

Virgina Community University Massey Comprehensive Cancer Center

Richmond, Virginia 23298-0037

United States

Peter MacCallum Cancer Centre

Melbourne, Victoria 3000

Australia

A.C.Camargo Cancer Center

São Paulo, São Paulo 105401

Brazil

Royal Victoria Regional Health Centre

Barrie, Ontario L4M 6M2

Canada

London Health Science Centre - Verspeeten Family Cancer Centre

London, Ontario N6A 5W9

Canada

Lakeridge Health

Oshawa, Ontario L1G 2B9

Canada

Odette Cancer Centre

Toronto, Ontario M4N 3M5

Canada

Princess Margaret Cancer Centre

Toronto, Ontario M5G2C4

Canada

CHU de Québec-Université Laval

Montreal, Quebec G1G 5X1

Canada

Hôpital Maisonneuve-Rosemont - CIUSSS de l'Est-de-l'Île-de-Montréal

Montreal, Quebec H1T 2M4

Canada

Centre hospitalier de l'Université de Montréal

Montreal, Quebec H2X 3E4

Canada

Clinica IRAM

Vitacura, Santiago Metropolitan 7630370

Chile

Tel-Aviv Sourasky Medical Centre

Tel Aviv,

Israel

AOU Careggi - Florence University Hospital

Florence,

Italy

King Hussein Cancer Centre

Amman, Jordan

Jordan

The Aga Khan University

Nairobi,

Kenya

Universitiy Malaya Medical Centre

Kuala Lumpur,

Malaysia