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N/A N=10 Treatment

Prone Breast Irradiation for Pendulous Breasts

Breast Cancer

Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Jan 2020
Primary outcome: Primary: Dose Homogeneity 1: PTV — 9.8; 8.2; 48.2; 49.8 Gy — p=<0.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Mamma board (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
Maastricht Radiation Oncology
Primary completion
Jul 2006

Outcome Measures

OutcomeResultp-value
PRIMARY
Dose Homogeneity 1: PTV
9.8; 8.2; 48.2; 49.8; 53.6; 54.8 <0.05 sig
PRIMARY
Dose Homogeneity 2: V105% and V107%
1.5; 9.1; 0.1; 2.8 <0.05 sig
PRIMARY
Dose Homogeneity 3: V95 %
78.6; 91.4; 85.0; 93.3 <0.05 sig
SECONDARY
PTV Coverage in Organs at Risk: MLD (Gy)
0.9; 4.1 <0.05 sig
SECONDARY
PTV Coverage in Organs at Risk: Heart V30
2.4; 7.3 <0.05 sig

Summary

We hypothesize that for large pendulous breasts, breast irradiation in supine and prone position are equivalent with regard to coverage of the PTV, but with a better dose homogeneity in prone position and a smaller radiation exposure of lung and heart.The purpose of this study is to compare the 3-D dose distribution in PTV(Planning Target Volume) and normal tissues in prone position versus supine position.

Eligibility Criteria

Inclusion Criteria

  • Patients should have had breast-conserving surgery for breast cancer or DCIS (Ductal Carcinoma in Situ)
  • No indication for radiotherapy of regional nodes
  • Large, pendulous breasts (bra size D and over)

Exclusion Criteria

  • Regional radiotherapy is indicated
  • Unable to lie in prone position
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00181363). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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