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Prognostic Indicators for Radiation-induced Breast Fibrosis

Identifying Prognostic Indicators for the Development of Radiation-induced Breast Fibrosis

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05031065
Enrollment
4
Registered
2021-09-01
Start date
2024-01-24
Completion date
2025-05-05
Last updated
2025-06-27

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

Conditions

Breast Cancer

Brief summary

To study the inflammatory response during and after radiotherapy, especially by measuring the concentration of an enzyme called autotaxin and its product LPA in the blood plasma.

Detailed description

To study the inflammatory response during and after radiotherapy, especially by measuring the concentration of an enzyme called autotaxin and its product LPA in the blood plasma. Autotaxin and LPA cause fibrosis in other situation, but they have not been tested in radiation-induced fibrosis. We will determine if the duration and magnitude of the autotaxin and LPA responses are prognostic for the 15-28% of patients who will develop fibrosis. This fibrosis will be detected by ultrasound and a novel application of elastography, which should provide much earlier and quantifiable fibrotic changes compared to conventional physical examination.

Interventions

RADIATIONBreast Cancer Radiotherapy

4000-4250 cGy in 15-16 daily fractions

Sponsors

AHS Cancer Control Alberta
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Female participants capable of giving informed consent, or if appropriate, participants having an acceptable individual capable of giving consent on the participant's behalf 2. Age 40 and above. 3. Treatment with breast conserving surgery. 4. Intended adjuvant whole breast radiotherapy dose to a dose of 40-42.5 Gy in 15-16 fractions. 5. Luminal A subtype as determined by clinipathologic factors (ER/PR positive, Her-2 negative, low Ki-67 or low OncotypeDx recurrence score

Exclusion criteria

1. Women who have smoked within the last 5 years 2. Patients requiring adjuvant chemotherapy. 3. Requirement for regional nodal radiotherapy. 4. Requirement for tumour bed boost. 5. Breast implants 6. Patients to be treated with partial breast irradiation. 7. Uncontrolled intercurrent illness or active infection. 8. Patients who have previously received chemotherapy. 9. Patients who have previously received chemotherapy.

Design outcomes

Primary

MeasureTime frameDescription
Measurement of the ATX-LPA (ATX) inflammatory response to standard RT for breast cancer as a prognostic marker for RT-induced fibrosis.Samples will be collected four times during RT treatment (3-4 weeks) and once every 3 months for an year.Measurement of longitudinal changes in plasma ATX in the irradiated breast.
Measurement of the ATX-LPA-inflammatory (LPA) response to standard RT for breast cancer as a prognostic marker for RT-induced fibrosis.Samples will be collected four times during RT treatment (3-4 weeks) and once every 3 months for an year.Measurement of longitudinal changes in plasma LPA in the irradiated breast.
Measurement of the ATX-LPA-inflammatory (cytokines) response to standard RT for breast cancer as a prognostic marker for RT-induced fibrosis.Samples will be collected four times during RT treatment (3-4 weeks) and once every 3 months for an year.Measurement of longitudinal changes in plasma cytokines in the irradiated breast.
Measurement of the ATX-LPA-inflammatory (chemokines) response to standard RT for breast cancer as a prognostic marker for RT-induced fibrosis.Samples will be collected four times during RT treatment (3-4 weeks) and once every 3 months for an year.Measurement of longitudinal changes in plasma chemokines in the irradiated breast.

Secondary

MeasureTime frameDescription
Acute Radiotherapy ToxicityThroughout the duration of the study, a total of 4 years .Radiotherapy associated toxicities will be assessed per CTCAE v5.0 by the study investigators.
Relationship with Cytomegalovirus infectionSeropositivity for CMV will be checked only at baseline.There is evidence that being infected with Cytomegalovirus is likely to increase the response of the autotaxin-lysophosphatidates inflammatory cycle in response to radiotherapy.
Structural changes in the irradiated breast and the non-irradiated breast3, 6, 12, 24 and 48 months after RTThe ultrasound procedure will provide a 3D analysis of the breast structure as well as a measurement of breast elasticity. Fibrotic changes in the breast will be measured by combining the 3D analysis and breast elasticity indices (median (kPa), IQR (kPA) and IQR/median (%))

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026