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Study identifier: NCT04472845 Synced from ClinicalTrials.gov · July 29, 2026
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HYPofractionated Adjuvant RadioTherapy in 1 Versus 2 Weeks in High-risk Patients With Breast Cancer (HYPART).

Condition: Breast Cancer · Hypofractionation · Radiotherapy Side Effect  ·  Sponsor: Post Graduate Institute of Medical Education and Research, Chandigarh

PhaseNA
Planned participants1018
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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 e…

This description comes directly from the study's public registry record.

Talk to the study team

BUDHI S YADAV, MD  ·  9815981176  ·  drbudhi@gmail.com

BUDHI S YADAV  ·  9815981176  ·  drbudhi@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Budhi Singh YadavChandigarh, IndiaRecruiting

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Source record: clinicaltrials.gov/study/NCT04472845