Ultra-Hypofractionated vs. Moderately Hypofractionated Proton Therapy for Early Breast Cancer After Lumpectomy

Recruiting now · Not applicable

Conditions studied: Breast Cancer, Proton Therapy

In brief

Breast-conserving surgery (BCS) followed by whole-breast irradiation (WBI) remains the standard therapeutic approach for early-stage breast cancer. Long-term follow-up data from the FAST trial (10-year analysis) demonstrated that the 28.5 Gy/5-fraction regimen exhibited comparable adverse effects to the conventional 50 Gy/25-fraction regimen, with no statistically significant differences in photographic cosmetic assessments at 2 and 5 years post-treatment. The FAST-Forward trial demonstrated comparable 5-year ipsilateral breast tumor recurrence rates (IBTR) and incidence of radiation-related toxicities between ultra-hypofractionated whole-breast irradiation (UH-WBI; 26 Gy in 5 fractions over 1 week) and moderately hypofractionated whole-breast irradiation (MH-WBI; 40 Gy in 15 fractions over 3 weeks). Additionally, no statistically significant difference in cosmetic outcomes was observed between the two regimens at the 2-year follow-up. Proton radiotherapy enables precise dose delivery to tumor targets while minimizing radiation exposure to surrounding normal tissues, thereby reducing treatment-related toxicities. However, current clinical protocols predominantly employ conventional fractionation for proton therapy, with a paucity of robust evidence evaluating the efficacy and safety of ultra-hypofractionated proton radiotherapy in breast cancer patients. This prospective randomized controlled trial aims to establish high-level scientific evidence for the clinical application of ultra-hypofractionated proton radiotherapy following BCS, ensuring non-inferiority in oncologic control, toxicity profiles, and cosmetic preservation compared to standard regimens.

Key facts

Study ID: NCT07135661
Run by: Shanghai Proton and Heavy Ion Center
People needed: 312
Starts: 2024-10-10
Expected to finish: 2029-10-31
Last updated by the study team: 2025-08-22

Who can join

Age: 40 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

Age ≥ 40 years
Pathologically (cytologically or histologically) confirmed unilateral primary invasive breast carcinoma
Breast conserving surgery + sentinel lymph node biopsy/axillary lymph node dissection, pathological stage pT1-2N0M0，negative margins (≥ 2 mm)
No distant metastasis confirmed by CT, MRI, bone scan, and PET/CT
No prior radiation therapy to the ipsilateral chest or breast
ECOG 0 \~ 2 or KPS ≥ 70

You may not qualify if…

Without pathology diagnosis
Positive margins or close margins (< 2mm)
Lymph nodes or distant metastasis
Bilateral breast cancer or patients with a history of contralateral breast cancer
Prior radiation therapy to the ipsilateral chest or breast
Pregnancy (confirmed by serum or urine β-HCG test) or lactation

Where it is running

Shanghai Proton and Heavy Ion Center — Shanghai, China (enrolling)

Full record on ClinicalTrials.gov

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