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Development of a Predictive Model for Skin Toxicity in Postmastectomy Breast Cancer Patients with Tomotherapy

Development of a Predictive Model for Late Radiation-Induced Skin Toxicity in Postmastectomy Breast Cancer Patients Treated with Tomotherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20260602003
Enrollment
246
Registered
2026-06-02
Start date
2020-02-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer Radiation-Induced Skin Toxicity Acute Radiation-Induced Skin Toxicity Late Radiation-Induced Skin Toxicity Breast cancer, Radiotherapy, Tomotherapy, Mastectomy, Radiodermatitis, Radiation Injuries, Logistic Models

Interventions

Breast cancer patients who received postmastectomy radiotherapy with Helical Tomotherapy at Buddhachinaraj Phitsanulok Hospital. Clinical, treatment-related, and dosimetric data will be collected retr
Other
Postmastectomy Breast Cancer Patients with Tomotherapy

Sponsors

Buddhachinaraj Phitsanulok Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Review medical records, including diagnostic reports, treatment records, and radiotherapy plans. 2. Patients will be considered eligible for inclusion if they meet the following criteria: 2.1 Female breast cancer patients aged 18 years or older, who are able to read and write, are willing to participate in the study, and provide written informed consent. 2.2 Received post-operative radiotherapy entirely using helical tomotherapy techniques. 2.3 Treated within the study period February 2020 to December 2024.

Exclusion criteria

Exclusion criteria: 1. Did not complete radiotherapy according to the prescribed treatment plan. 2. Were lost to follow-up after completion of radiotherapy. 3. Had incomplete data that prevented outcome assessment according to the study endpoints. 4. Declined participation in the clinical evaluation or did not consent to the use of their data for further study.

Design outcomes

Primary

MeasureTime frame
Late Radiation-Induced Skin Toxicity More than 3 months after completion of radiotherapy RTOG/EORTC criteria

Secondary

MeasureTime frame
Acute Radiation-Induced Skin Toxicity During radiotherapy treatment course RTOG/EORTC criteria

Countries

Thailand

Contacts

Public ContactWanwisa Bumrungpagdee

Buddhachinaraj Phitsanulok Hospital

kureekureekuree@gmail.com0911948118

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026