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Comparing 5 and 15 Fractions for Whole Breast Irradiation After Breast Conserving Surgery

Not Applicable
Completed
Conditions
Breast Cancer
Interventions
Radiation: Radiation
Registration Number
NCT03677427
Lead Sponsor
University Hospital, Ghent
Brief Summary

Adjuvant radiotherapy after breast-conserving surgery for breast cancer reduces the risk of locoregional relapse and ensures better overall survival. In recent years it has been found that hypofractionation in which the number of radiation sessions is reduced with a higher dose per session offers advantages for breast irradiation. Randomized studies showed that moderate hypofraction regimens in 15 or 16 fractions have the same effect in tumor control and toxicity, although the total dose is lower than the traditional 50 Gy in 25 fractions. In a randomized study from the United Kingdom (START-B trial) even a better disease-free survival was seen with 15 sessions than with 25 sessions and the long-term side effects were also less with the short schedule.

This project proposes a clinical trial with an accelerated radiotherapy schedule in 5 sessions. It is expected that the accelerated schedule of 5 sessions over 12 days will have a number of radiobiological benefits: since a higher dose per session is given over a shorter period of time, it is expected that tumor control and survival will be higher. By reducing the total treatment time, the total dose is reduced, which may result in fewer radiation-related side effects and thus improve the quality of life. Apart from these radiobiological benefits, the shorter radiotherapy program reduces the number of treatment days from 15 to 5. This is not only more comfortable for the patients, but also increases the treatment capacity of the radiotherapy department. This opens up a possibility for the use of more complex techniques with fewer side effects such as radiation in the prone position.

This project includes a randomized study comparing the accelerated schedule in 5 sessions with a hypofraction schedule of 15 sessions in patients who are irradiated on the entire breast after breast-saving surgery. The primary endpoint is chest retraction (loss of volume) 2 years after radiotherapy.

Detailed Description

Adjuvant radiotherapy after breast conserving surgery for breast cancer reduces the locoregional recurrence rate and improves overall survival. In recent years, it has become clear that breast cancer cells are more sensitive to fraction dose than originally presumed. Large randomized trials confirm this hypothesis: moderate hypofractionation schemes in 15 or 16 fractions are at least equivalent in tumor control and toxicity although the total dose is lower than the traditional 50 Gy in 25 fractions. Further acceleration to 5 fractions is expected to have an even larger radiobiological advantage regarding tumor control. Additional advantages are patient comfort and a better use of radiotherapy resources. Due to capacity problems some radiotherapy departments are faced with waiting lists which not only delay the time between surgery and radiotherapy, but also interfere with the introduction of more sophisticated treatment techniques like prone whole-breast irradiation (WBI). Prone WBI has several advantages over supine WBI: less acute skin toxicity and improved breast cosmesis and reduced doses to heart and lung leading to less radiation-induced heart diseases and secondary lung cancer induction.

Hypofractionation and acceleration (shorter radiotherapy schemes with less fractions and a higher dose per fraction) are attractive both for the patient (less treatment sessions) and for the hospital (more treatment capacity and shorter waiting lists). Moderate hypofractionation in 15 or 16 fractions has been generally accepted as a valid alternative for the historical schedules of 25-30 fractions for whole-breast irradiation (WBI) after breast conserving surgery (BCS). With a median follow-up of 9.9 years, the UK START-B trial showed no significant difference in locoregional control between a hypofractionated schedule of 40.05 Gy in 15 fractions and a normofractionation scheme of 50 Gy in 25 fractions1. The Canadian schedule of 42.5 Gy in 16 fractions was also not inferior to the 50 Gy/25 fractions after 10 years of follow-up2. Aside from the obvious advantage of shortening the overall treatment time from 5 weeks to 3 weeks, both for the patient and the radiotherapy department, there might be some radiobiological advantages too. In the START-B trial, breast shrinkage, telangiectasia and breast oedema were significantly less frequent in the hypofractionation group. Better disease free survival and overall survival were also reported in the 15 fractions group, due to less distant relapses. The superiority of hypofractionation on survival and cosmesis was not observed in the Canadian trial.

While Belgium is a country with extensive health care facilities, some countries have a limited number of radiotherapy departments and patients have to travel a long distance for radiation. In those countries the pressure to evolve to even more retracted radiotherapy schemes is high. WBI in 5 fractions of 5.7 Gy over 5 weeks was tested in the FAST trial. A first analysis after 3 years demonstrated equivalence in toxicity and tumor control in comparison with the standard prescription of 25 x 2 Gy3. This accelerated schedule is in particular attractive for older patients since they often face logistic problems (frailty, impaired mobility, transportation difficulties). This sometimes leads to omission of radiotherapy leading to a reduced breast cancer specific survival4,5. For this reason, at UZ Gent a feasibility trial was started testing a highly accelerated schedule in 5 fractions over 12 days in patients of 65 years or older. The investigators used the FAST-scheme for WBI (5 x 5.7 Gy), but also included patients requiring a boost (5 x 6.5 Gy). With patient inclusion nearly finished, an interim analysis shows \<10% grade 2-3 erythema, with only one case of moist desquamation, located at a skin fold6. In this study the investigators propose a multi-center randomized trial comparing our accelerated schedule in 5 fractions with a moderate hypofractionation scheme of 15 fractions in patients treated with WBI. The primary endpoint is breast retraction 2 years after radiotherapy.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
488
Inclusion Criteria
  • female patients with non-metastatic breast cancer,
  • age ≥ 18 years,
  • breast conserving surgery,
  • multidisciplinary decision of adjuvant breast irradiation,
  • informed consent obtained, signed and dated before specific protocol procedures
Exclusion Criteria
  • lymph node metastases,
  • distant metastases,
  • bilateral breast irradiation,
  • history of previous radiation treatment to the same region
  • life expectancy of less than 2 years,
  • planned reconstructive surgery,
  • conditions making toxicity evaluation difficult (e.g. skin disorders),
  • inability to respect constraints on organs at risks
  • patients unlikely to comply with the protocol

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
15 fractionsRadiation-
5 fractionsRadiation-
Primary Outcome Measures
NameTimeMethod
radiation-induced breast retraction4 years

The primary endpoint of the randomized trial is radiation-induced breast retraction (volume loss) measured 2 years after radiotherapy.$

Secondary Outcome Measures
NameTimeMethod
Acute breast toxicity: cough2 years

Cough, Common Terminology Criteria for Adverse Events v4.03

Acute breast toxicity: dermatitis2 years

Dermatitis, Common Terminology Criteria for Adverse Events v4.03

Acute breast toxicity: desquamation2 years

Desquamation, Common Terminology Criteria for Adverse Events v4.03

Acute breast toxicity: breast oedema2 years

Oedema, Common Terminology Criteria for Adverse Events v4.03

Acute breast toxicity: breast symptoms2 years

pain, sense of heaviness, itching

Acute breast toxicity: dyspnoea2 years

Dyspnoea, Common Terminology Criteria for Adverse Events v4.03

Late toxicity other than breast retraction: dyspnoe5 years

Dyspnoe, Common Terminology Criteria for Adverse Events v4.03

Late toxicity other than breast retraction: pain5 years

Pain, Common Terminology Criteria for Adverse Events v4.03

Late toxicity other than breast retraction: breast symptoms5 years

Pain, sense of heaviness, itching

Acute breast toxicity: pain2 years

Pain, Common Terminology Criteria for Adverse Events v4.03

Late toxicity other than breast retraction: breast oedema5 years

Breast oedema, Common Terminology Criteria for Adverse Events v4.03

Late toxicity other than breast retraction: telangiectasia5 years

Telangiectasia, Late Effects Normal Tissue Task Force (LENT)-Subjective, Objective, Management, Analytic (SOMA) scales

Late toxicity other than breast retraction: colour changes5 years

Colour changes, Common Terminology Criteria for Adverse Events v4.03

Late toxicity other than breast retraction: fibrosis5 years

Fibrosis, Late Effects Normal Tissue Task Force (LENT)-Subjective, Objective, Management, Analytic (SOMA) scales

Trial Locations

Locations (1)

Radiotherapie UZ Gent

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Gent, Oost-Vlaanderen, Belgium

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