Clinical trial Recruiting at 1 site Observational Ages 18 and up Women only

How breast radiotherapy technique works best for each patient

Official title: Analysis of Anatomical Parameters in the Radiotherapy of Breast Cancer

Run by Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCS · NCT07881341 · Data updated 2026-11-12

This study tests three radiotherapy plans (3D-CRT, IMRT S&S, and a hybrid) for left breast cancer to see which best fits each patient.

More Breast Cancer trials

Quick facts

Study typeObservational
Ages18 Years and up
SexWomen only
Enrollment30 (estimated)
SponsorIstituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCS
Academic / other
Drugs / interventionsRadiation
Locations1 site (Meldola, FC)
StatusRecruiting
StartedJune 16, 2023
Main results expectedNovember 2026
Study endsDecember 2026
Registry record updatedOctober 19, 2026
Trial IDNCT07881341 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adult women with left breast cancer who are eligible for radiotherapy and can provide informed consent.

Probably not a fit

Patients whose anatomy or disease characteristics do not favor one technique over others may not experience a clear benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective observational study enrolls at least 30 female patients with left breast cancer to compare three planned radiotherapy techniques. Each patient will have 90 treatment plans simulated (three plans per patient) and the best technique will be chosen by at least three expert clinicians using a scoring system. No changes to standard clinical practice will be made and all data reflect routine care collected during treatment planning and follow-up. The study aims to identify objective criteria that could guide future selection of radiotherapy techniques for individual patients. The duration is expected to be about 30 months and all treatments will use a dose of 40.05 Gy in 15 fractions.

Why it matters

Potential benefit: If successful, the study could help clinicians choose the most appropriate radiotherapy technique for each patient, potentially improving treatment effectiveness and reducing side effects.

How similar studies have gone: Previous work in radiotherapy planning shows benefit from comparing techniques, but this exact a priori matching approach is novel in this setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Female
* Target volume: left breast
* Tumor type: any diagnosis of breast cancer
* Dose prescription: 40.05 Gray/15 fractions
* Patients aged ≥ 18 years old
* Patients willing and able to give informed consent to participate

Exclusion Criteria:

* Other concomitant tumor lesions
* Sovraclavear lymph node involvement

Where it's running

  • Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori - IRST IRCCS
    Meldola, Fc, Italy
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.