Observation: No postoperative radiotherapy will be administered. Patients will receive close surveillance after surgery.
Endocrine Therapy (Optional): Adjuvant endocrine therapy may be administered according to physician discretion and patient preference.
Study summary
This is a single-center, prospective phase II clinical study designed to evaluate whether omission of postoperative radiotherapy is clinically acceptable in young patients with low-risk ductal carcinoma in situ (DCIS) following breast-conserving surgery. Eligible patients include women younger than 40 years with low- or intermediate-grade DCIS, tumor size ≤1 cm, negative surgical margins ≥3 mm, absence of comedo necrosis, and unifocal screen-detected disease. Patients in the radiotherapy omission cohort will undergo close surveillance after surgery, with endocrine therapy permitted according to physician discretion. The primary endpoint is 5-year ipsilateral breast tumor recurrence (IBTR).
Eligibility
Sex
FEMALE
Min age
—
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria:
1. Female patients aged \<40 years；
2. Histologically confirmed low- or intermediate-grade ductal carcinoma in situ (DCIS) without invasive carcinoma, including incidental DCIS identified within benign breast lesions；
3. Tumor size ≤1 cm on final pathology；
4. Negative surgical margins ≥3 mm, including margins obtained after re-excision；
5. Unifocal lesion；
6. Absence of comedo necrosis；
7. Screen-detected disease without bloody nipple discharge or palpable mass；
8. Clinically node-negative disease；
9. Central pathology review by the participating institution required；
10. Ability to understand and willingness to sign written informed consent.
Exclusion Criteria:
1. Known BRCA1, BRCA2, or TP53 germline mutation carriers (genetic testing not mandatory)；
2. Bilateral breast cancer or prior contralateral breast cancer；
3. Severe uncontrolled comorbidities, including significant cardiac, pulmonary, hepatic, renal, hematologic, or psychiatric disorders；
4. History of other malignancies, including thyroid cancer, except adequately treated basal cell carcinoma of the skin or cervical carcinoma in situ；
5. Pregnant or breastfeeding patients；
6. Estimated life expectancy ≤5 years；
7. Poor compliance or inability to adhere to study follow-up requirements.
Primary outcome measure(s)
Ipsilateral Breast Tumor Recurrence (IBTR) — 5 years Defined as recurrence of invasive carcinoma or DCIS in the ipsilateral breast.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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