Partial Breast Re-irradiation for Breast Cancer

Trial statusActive, not recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity Hospital Heidelberg

About this trial

Breast cancer is the most common malignancy in women. Breast-conserving surgery (BCS) with adjuvant whole-breast irradiation (WBI) is currently the standard of care in the oncological treatment of primary breast cancer and offers an equivalent alternative to mastectomy. The primary aim of adjuvant radiotherapy (RT) is to improve local control and thus improve overall survival and breast cancer-specific mortality. However, nodal-negative women have a 10-year risk for local recurrences after RT in up to 15.6%. The management of ipsilateral breast cancer recurrence depends on the extent of tumor disease and staging results at the time of recurrence and mastectomy is currently the standard of care for previously irradiated patients. The application of particle therapy using proton beam therapy (PBT) represents an innovative radiotherapeutic technique for breast cancer patients. This trial will be conducted as a prospective single-arm phase II study in 20 patients with histologically proven invasive breast cancer recurrences with negative margins after repeat BCS and with an indication for local re-irradiation. Required time interval will be 1 year after previous RT to the ipsilateral breast. Patients will receive partial breast re-RT with proton beam therapy in 15 once daily fractions up to a total dose of 40.05 GyRBE. The primary endpoint is defined as the cumulative overall occurrence of acute / subacute skin toxicity grade ≥3 within 6 months after the start of re-RT.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

histologically confirmed recurrent (or new primary) ipsilateral invasive breast cancer or DCIS after prior RT of the ipsilateral breast

indication for re-irradiation after repeat breast conserving surgery (e.g. lumpectomy, wide excision, …)

tumor size < 3 cm

clinically node-negative (cN0)

Disqualifiers

distant metastases

concomitant chemotherapy (concomitant endocrine hormonal therapy is allowed; sequential chemotherapy is allowed)

patients who have not recovered from acute toxicities of prior therapies

known carcinoma < 5 years ago (excluding Carcinoma in situ of the cervix, basal cell carcinoma, squamous cell carcinoma of the skin) requiring immediate treatment interfering with study therapy

Trial design

Design model

Single group

Treatments tested in this trial

  • Radiation Therapy

    Radiation

    proton beam radiation

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: Proton beam therapyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

skin toxicity

Occurrence of overall acute / subacute skin toxicity CTCAE grade 3 or higher (NCI CTCAE version 5.0) assessed.

Time frame
Within the first 6 months after the start of re-RT

Secondary outcomes

1

Local Tumor control

presence of tumor cells on initial tumor site

Time frame
At 1, 2 and 5 years after re-RT
2

Patients Quality of life

quality of life (EORTC QLQ-C30 and the supplementary questionnaire module QLQ-BR42 measuring specific quality of life aspects related to breast cancer treatment)

Time frame
At 1, 2 and 5 years after re-RT
3

Regional Tumor control

presence of tumor cells on initial tumor region

Time frame
At 1, 2 and 5 years after re-RT
4

Distant Tumor control

presence of tumor cells on distant tumor site

Time frame
At 1, 2 and 5 years after re-RT

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: