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Prone Breast Radiotherapy Treatment Planning Observational Study

Retrospective Dosimetric Study of Prone Radiotherapy for Breast Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02237469
Acronym
HUGProne
Enrollment
280
Registered
2014-09-11
Start date
2010-09-30
Completion date
2023-12-31
Last updated
2022-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer Female

Keywords

Breast cancer, Breast conserving surgery., Radiotherapy., Treatment planning., Prone.

Brief summary

The study purpose is to evaluate whether or not clinical characteristics of women with breast cancer can predict which position for radiation treatment, prone or supine, will be associated with a dosimetry gain. Dosimetry gain in this study means the lowest radiation dose to non-target organs (heart, lungs, contralateral breast), while giving the prescribed dose to tumor bed and ipsilateral breast.

Detailed description

Retrospectively identify women who received curative radiation treatment after breast conserving cancer surgery, in whom simulation in prone and in supine position was performed. Compare the treatment plans for doses to targets and to non-target organs, according to clinical parameters of body mass index, size of breast, location of tumor and side. Furthermore, evaluate whether a single CT slide is enough or not to predict a dosimetry advantage.

Interventions

RADIATIONProne and supine simulation

Treatment planning in the two positions.

Sponsors

Varian Medical Systems
CollaboratorINDUSTRY
Vincent Vinh-Hung
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Breast conserving surgery * Adjuvant radiation treatment * Simulation done prone and supine

Exclusion criteria

* Simulation in only one position

Design outcomes

Primary

MeasureTime frameDescription
Radiation dose to heart and lungs4 monthsComputations of doses and verification of physics charts.

Secondary

MeasureTime frameDescription
Radiation dose to tumor bed and ipsilateral breast4 monthsComputations of doses and verification of physics charts.

Other

MeasureTime frameDescription
Numbers of patients with dosimetry gain in prone position2 yearsEvaluate the dosimetry gain in subgroups classified according to body mass index, size of breast, side and location of tumor.

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026