Recruiting
Phase 3

Radiation Therapy

Sponsor:

M.D. Anderson Cancer Center

Code:

NCT05774678

Conditions

Breast Cancer

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Group 1 (preoperative radiation hypofractionated)

Group 2 (preoperative radiation conventionally fractionated)

Study Details

Brief summary:

To compare the outcomes of and responses to 2 different radiation therapy schedules (the standard radiation amount and number of doses versus less radiation and fewer doses) that are being given before having breast cancer surgery (cancer removal and reconstruction).

Conditions

Breast Cancer

Study ID

NCT05774678

Start date

Apr 5, 2023

Status verified date

Jun, 2026

Completion date

Nov 1, 2028

Anticipated

Primary completion date

Nov 1, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Age 18 years or older
  • Histologic diagnosis of invasive breast cancer (cytologic or histologic confirmation of nodal metastasis is sufficient to establish this eligibility criteria).
  • Clinical and/or pathologic stage T3-T4c OR N1-N3; for the IBC pilot cohort only, the stage requirement is T4d, any N, M1
  • Mastectomy is the planned oncologic surgery but has not yet been performed at the time of protocol enrollment
  • Autologous (i.e. tissue-based) reconstruction is planned with either a free or rotational flap.
  • For patients with HER2 positive, non-IBC breast cancer treated with neoadjuvant chemotherapy, one of the following criteria must be met:

1. Residual invasive disease should be documented in either the breast or a regional nodal metastasis after neoadjuvant chemotherapy. This specific eligibility criteria can be satisfied by the post-chemotherapy standard of care breast biopsy. For this matter, the patient may be enrolled on the trial prior to biopsy. If the biopsy does not show residual invasive disease, then the patient will not proceed with protocol-directed therapy and will be removed and replaced from the study.
2. Medical oncologist has documented a discussion in the chart about potential risks of proceeding with PreMRT with regard to impact on adjuvant systemic therapy decisions and the patient has opted to proceed with trial enrollment
  • For T4d pilot cohort patients, post-chemotherapy, pre-radiation ultrasound must demonstrate at least partial response in the breast and regional lymph nodes and no suspicious infraclavicular, internal mammary, and supraclavicular lymph nodes.
  • Ability to provide written informed consent in accordance with institutional policies.

Exclusion Criteria:

  • Patients undergoing treatment for recurrent breast cancer in the index breast or lymph nodes.
  • History of therapeutic irradiation to the breast, lower neck, mediastinum or other area(s) that will overlap with the affected breast.
  • Presence of active scleroderma
  • Patients who are pregnant.

Study Design

Enrollment

126 participants

Anticipated

Allocation

Randomized

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Group 1 (preoperative radiation hypofractionated)

Participants will receive the standard number of radiation treatment doses

experimental: Group 2 (preoperative radiation conventionally fractionated)

Participants will receive the standard number of radiation treatment doses

Interventions

Group 1 (preoperative radiation hypofractionated)

radiation schedules/regimens before your scheduled breast surgery

Group 2 (preoperative radiation conventionally fractionated)

radiation schedules/regimens before your scheduled breast surgery

Primary outcome measure

  • Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0 [ Time Frame: through study completion; an average of 1 year. ]

Central Contacts and Locations

Central contacts

Locations

M D Anderson Cancer Center

Recruiting

Houston, Texas, United States, 77030

Contacts

Principal Investigator:

Benjamin D. Smith, MD

More Information

Sponsor

M.D. Anderson Cancer Center

Last update posted

Jun 23, 2026

Last verified

Jun, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by M.D. Anderson Cancer Center on 2026-06-23.