RecruitingNot ApplicableNCT04472845

HYPofractionated Adjuvant RadioTherapy in 1 Versus 2 Weeks in High-risk Patients With Breast Cancer (HYPART).

HYPofractionated Adjuvant RadioTherapy in 1 Versus 2 Weeks in High-risk Patients With Breast Cancer (HYPART): A Non-inferiority, Open-label, Phase III Randomized Trial.


Sponsor

Post Graduate Institute of Medical Education and Research, Chandigarh

Enrollment

1,018 participants

Start Date

Mar 30, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

We at PGIMER have been practicing hypofractionated radiotherapy in breast cancer patients for the last 4 decades. Our standard doses have been 35Gy/15#/3wks to the chest wall after mastectomy and 40Gy/16#/3wks after breast conserving surgery (BCS).It is also a routine practice in the UK and in a few centers in Canada. Hypofractionation reduces treatment time to half while maintaining cosmesis and gives control rates equal to conventional fractionation. As breast cancer is a leading cancer in females and radiation therapy is an important part of its local management, hypofractionation helps radiation centers worldwide to meet the growing need for radiation treatment in breast cancer, particularly in developing countries where resources are limited. It also reduces the financial burden on the patient and family. In this study we want to evaluate the impact of reducing the treatment duration from 3 weeks to 1 week. Eligible patients with breast cancer after mastectomy or BCS will be treated with a radiotherapy dose of 26Gy in 5 fractions over 1 week in the study arm and 40Gy in 15 fractions over 2 weeks in the control arm. The primary endpoint of this noninferiority study will be locoregional tumour control. Secondary endpoints will be early and late radiation toxicities, quality of life, contralateral primary tumours, regional and distant metastases, survival and second cancers. A total of 1018 patients will be randomised (1:1) to receive 1 week or 2 weeks of radiotherapy. An event-driven analysis will be performed after at least 94 patients have documented locoregional recurrences.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing two schedules of radiation therapy after breast cancer surgery — a 1-week course versus a 2-week course — in patients with high-risk breast cancer. The goal is to see whether the shorter course works just as well and has comparable side effects to the standard 2-week schedule. **You may be eligible if:** - You are 18 or older (male or female) - You have invasive breast cancer - You have had breast-conserving surgery or total mastectomy with lymph node removal - Your cancer is stage pT3-4 or pN2-3, or clinical stage III (including after neoadjuvant chemotherapy) - Your surgery completely removed the tumor **You may NOT be eligible if:** - Your cancer has spread to distant lymph nodes (supraclavicular, internal mammary) or other organs - You have had another cancer in the past (with exceptions for basal cell skin cancer, CIN of the cervix, or cancers treated with curative intent at least 5 years ago) - You have cancer in the other breast - Your breast reconstruction uses implants - You are pregnant - You are currently receiving cytotoxic chemotherapy at the same time as radiation (sequential chemo before or after is allowed) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

RADIATION1 week RT

RT will be delivered over 1 week

RADIATION2 week RT

RT will be delivered over 2 week


Locations(1)

Budhi Singh Yadav

Chandigarh, India

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT04472845


Related Trials