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A pilot study of hypofractionated nodal irradiation for postoperative breast cancer

A pilot study of hypofractionated nodal irradiation for postoperative breast cancer - FRONTIRE

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000051553
Enrollment
20
Registered
2023-07-08
Start date
2023-07-04
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Breast cancer

Interventions

Mild hypofractionated postoperative radiation therapy 42.56 Gy in 16 daily fractionations for patients with high-risk breast cancer.

Sponsors

Hyogo Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Postoperative breast cancer patients who meet the indication criteria for adjuvant radiation therapy including chest wall/conserved breast and regional lymph node in Hyogo Cancer Center Breast Cancer Guidelines.

Exclusion criteria

Exclusion criteria: Patients with malignancy other than breast cancer, infective disease requiring systemic therapy, fever (> 100 F), diabetes mellitus (HbA1c => 7.0 %), lung fibrosis/interstitial lung disease/severe emphysema, active collagen vascular disease, or genetic disorders high-risk for radiation. Patients who are (possibly) pregnant, breast feeding, receiving systemic steroids or immune-suppression therapy, planned to have breast reconstruction surgery, unable to raise her/his arms above shoulders, or receiving radiation therapy including internal mammary node region.

Design outcomes

Primary

MeasureTime frame
Acute or subacute adverse events of CTACE grade 2+ occurring within 6 months from radiation therapy completion

Countries

Japan

Contacts

Public ContactHaruka Uezono

Hyogo Cancer Center Department of Radiation Oncology

haru770911@yahoo.co.jp0789291151

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026