Trials / Completed
CompletedNCT01278212
Accelerated Hypofractionated Radiotherapy (AHF-RT) for the Treatment of Breast Cancer
A Phase II Study of Accelerated Hypofractionated Radiotherapy (AHF-RT) After Breast Conserving Surgery (BCS) in Medically Underserved Patients
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 158 (actual)
- Sponsor
- University of Louisville · Academic / Other
- Sex
- Female
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
The goal of this study is to explore the safety, effectiveness, quality of life, and cost effectiveness of accelerated hypofractionated radiotherapy (AHF-RT) as treatment after lumpectomy in patients with early stage breast cancer.
Detailed description
The traditional radiation treatment schedule for patients who have had a lumpectomy for early stage breast cancer is 15 to 30 treatments delivered once a day for 3 to 6 weeks. This treatment schedule can be inconvenient and costly for elderly, rural, uninsured, and minority patients. This study will evaluate a new radiation treatment schedule called whole-breast accelerated hypofractionated radiotherapy (AHF-RT). AHF-RT delivers higher doses of radiation in fewer treatments than traditional radiation therapy. The AHF-RT treatment course is completed with 5 radiation treatments delivered once a week for 5 weeks. The purpose of this study is to determine if accelerated hypofractionated radiotherapy (AHF-RT) is a safe, effective, more convenient, and less costly alternative to traditional radiation that will offer the same chance of cure with no additional side effects.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| RADIATION | accelerated hypofractionated radiotherapy (AHF-RT) | 30 Gy in 5 fractions once a week for 5 weeks, followed by optional boost of 10-16 Gy |
Timeline
- Start date
- 2011-01-01
- Primary completion
- 2021-01-27
- Completion
- 2021-01-27
- First posted
- 2011-01-17
- Last updated
- 2024-02-22
- Results posted
- 2024-02-22
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01278212. Inclusion in this directory is not an endorsement.