Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Locoregional Recurrence
  • Radiotherapy Side Effect
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Double (Care Provider, Investigator)Primary Purpose: Other

Participation Requirements

Age
Between 18 years and 75 years
Gender
Only males

Description

166 patients of breast cancer patients after mastectomy ( 83 patients in each arm ) will be randomize into 2 hypofractionation arms : Arm A: 40 Gy /15 fx / 3 weeks, 5 days per week . Arm B: 28.5 Gy delivered in 5 once-weekly fractions of 5.7 Gy each week. Simulation: Patient will be simulated on CT ...

166 patients of breast cancer patients after mastectomy ( 83 patients in each arm ) will be randomize into 2 hypofractionation arms : Arm A: 40 Gy /15 fx / 3 weeks, 5 days per week . Arm B: 28.5 Gy delivered in 5 once-weekly fractions of 5.7 Gy each week. Simulation: Patient will be simulated on CT simulator using breast wedge with angle. Serials will be taken every 2 mm from upper neck down to mid abdomen. Contouring: CTVcw, CTVRNI will be contoured through RTOG guidelines . PTV is added as 0.5 cm all around CTV. Lungs, Heart, brachial plexus, spinal cord, esophageus and thyroid will be contoured as OAR. (www.rtog.org/CoreLab/ContouringAtlases/BreastCancerAtlas.aspx). D)Dose Constraints: Arm A: PTV EVAL ( CW) : V90 % ? 90 %. - V105 % ? 5% - V107%? 3 %. Ipsilateral lung: V20 less than 20-25% - V 8 less than 35%- Contra lateral lung: V4 less 10 %. Heart: V16 less than 5% (Lt sided). V20 less than 5% (Lt sided). V16 is 0%.(Rt sided) V20 is 0% (Rt sided). Mean heart dose ? 320-400 cGy. Contra lateral breast : D max? 240 cGy. V 144 cGy less than 5 %. SCV : V90 % ? 90 %. Thyroid : Mean dose less than 35 Gy - V30 less than 50 %. Arm B: PTV EVAL ( CW) : V90 %? 90 %. - V105 %? 5% - V107%? 2 %. Ipsilateral lung: V30%less than 15 -20% - V15% less than 30-35% - V5 % less than 50-55%. Contra lateral lung : V5 % less than 5%. Heart :V25 % less than 5 % - V5 % less than 30 - 35 %. Contra lateral breast: V3 % less than 5 %. SCV : V90 % ? 90 %. Follow up: A)Weekly follow up will be done during sessions then regular clinical exam every 3 months to assess : Acute and late toxicity regarding pain, pulmonary toxicity, dysphagia, skin toxicity and lymphedema.Assessment will be done according to RTOG and CTCv.5. Any local (chest wall) recurrence, regional (nodal) recurrence. B)Annual Mammogram. C)Any another investigation (once indicated)

Tracking Information

NCT #
NCT04550910
Collaborators
Not Provided
Investigators
Principal Investigator: Osama Yousof, MD National Cancer Institute, Egypt