Study for people with Breast Cancer

Not yet recruiting Not a phased study

Sources: ClinicalTrials.gov Checked: 11 October 2026 Not medical advice

This trial at a glance

Status Not yet recruiting
Phase Not a phased study
Sponsor Integrated Community Oncology Network
Registry number NCT06909032
Started 1 April 2025 Today 16 October 2026 Estimated completion 1 July 2030

Where this trial is running

Trial sites and the status recorded for each
SiteCityState or countryStatus at this site
Icon Cancer Centre Wahroonga Wahroonga NSW Status not stated
Icon Cancer Centre Windsor Gardens Windsor Gardens SA Status not stated

voxsanity.com.au · trial sites from public registries · registry record synced 11 October 2026 · not medical advice

Who can join

Age 50 Years and over
Sex Female participants only
Healthy volunteers Not accepted
Enrolment target 168

The official eligibility criteria

Registry text, reproduced exactly. These are the words the trial's sponsor published on ClinicalTrials.gov. They have not been edited, shortened or rewritten, and they are written for researchers rather than for patients.

Inclusion Criteria:

* Aged greater than or equal to 50 years old

* Histologically confirmed Infiltrating ductal carcinoma (IDC) or pure DCIS, less than or equal to 20mm maximum size.

* Lobular carcinoma in situ (LCIS) is permitted.

* Histologic grade I or II

* Estrogen receptor (ER) +/- progesterone receptor (PR) positive in greater than or equal to 10% of cells and HER2 receptor-negative.

* Tumour bed identifiable on imaging via surgical clips

* Clear surgical margins

* Sentinel nodes negative (at least one node taken if invasive and no isolated tumour cells)

* No evidence of distant metastasis

Exclusion Criteria:

* Ink on surgical margins or positive histological margins

* Lymphatic vessel invasion (LVI)

* Bilateral breast cancer

* Invasive lobular carcinoma

* Pleomorphic LCIS

* Multifocal or multicentric invasive cancer

* Invasive carcinoma with associated DCIS greater than or equal to 30mm.

* Patients receiving neoadjuvant chemotherapy, anti-HER2 agents or endocrine therapy

* Patients receiving adjuvant chemotherapy or anti-HER2 agents.

* Previous Hodgkin's lymphoma requiring mantle radiation

* Prior radiation therapy to the ipsilateral breast

* Triple-negative breast cancer

* Documented mutation of BRCA1, BRCA2 or TP53, or at high genetic risk of breast cancer

* Known inflammatory conditions associated with higher complications after RT, such as active scleroderma, systemic lupus erythematosus (requiring steroids or immune suppressive therapy)

* Oncoplastic surgery where the primary tumour site is difficult to delineate

* No previous cancer (except BCC or SCC of the skin) unless in remission beyond five years of diagnosis

* People who are pregnant or planning to become pregnant

* People who are unable or unwilling to comply with protocol requirements.

Dates on the record

Started 1 April 2025
Estimated completion 1 July 2030
Registry last updated 3 April 2025
Checked by Voxsanity 11 October 2026

Results, publications and the official record

Sources and dates

  • ClinicalTrials.gov – the record this page reformats
  • ClinicalTrials.gov processing date: 3 April 2025.
  • This page last checked by Voxsanity: 11 October 2026.

Voxsanity reformats data from public registries into this layout. It does not edit, interpret or add to what the registry published.

Not medical advice.

Individual trial records are refreshed on a rolling basis rather than all at once, so a record may be up to several weeks old. Each trial page and trial card shows the date its own record was last synced. Where a record has lagged, its status, sites and enrolment can differ from the current registry state in either direction, so check the registry link on the trial page before acting on them.

Letter for your doctor

A one-page summary of this trial to print or email to your GP. It carries the registry's own record of the trial and its eligibility criteria, and nothing Voxsanity has written about whether it suits you.