Clinical Trials Directory

Trials / Unknown

UnknownNCT01322854

Adjuvant Whole Breast Radiotherapy (RT) With Intensity Modulated Radiotherapy (IMRT) and a Simultaneous Integrated Boost Versus Conventional RT and a Sequential Boost

Randomized Phase III Trial Comparing Intensity Modulated Radiotherapy With Integrated Boost to Conventional Radiotherapy With Consecutive Boost in Patients With Breast Cancer After Breast Conserving Surgery

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
502 (estimated)
Sponsor
Heidelberg University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The IMRT-MC2 study is a prospective, two armed, multicenter, randomized phase-III-trial comparing intensity modulated radiotherapy with integrated boost to conventional radiotherapy with consecutive boost in patients with breast cancer after breast conserving surgery. 502 patients will be recruited and randomized in two arms: patients in arm A will receive IMRT in 28 fractions delivering 50.4 Gy to the breast and 64.4 Gy to the tumor-bed by an integrated boost, while patients in arm B will receive conventional radiotherapy of the breast in 28 fractions to a dose of 50.4 Gy and a consecutive boost in 8 fractions to a total dose of 66.4 Gy. Primary aim of the study is the assessment of the cosmetic outcome and local control after breast radiotherapy. The study hypothesis is that intensity modulated radiotherapy (IMRT) is, in spite of the reduced treatment duration, at least equivalent to conventional therapy.

Conditions

Interventions

TypeNameDescription
RADIATIONIMRT with an simultaneous integrated boostIMRT in 28 fractions delivering 50.4 Gy to the whole breast and 64.4 Gy to the tumor-bed

Timeline

Start date
2011-03-01
Primary completion
2013-03-01
Completion
2018-03-01
First posted
2011-03-25
Last updated
2011-04-07

Locations

2 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT01322854. Inclusion in this directory is not an endorsement.