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OncoMatch/Clinical Trials/NCT04356209

Improving Theempowerment in Patients With Severe Breast Fibrosis Radio-induced Treated by Pravastatin : Benefit of e-PROs (Electronic " Patient Reported Outcome ") on Breast-related Quality of Life

Is NCT04356209 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Pravastatin for breast cancer.

Phase 2RecruitingInstitut du Cancer de Montpellier - Val d'AurelleNCT04356209Data as of May 2026

Treatment: PravastatinConserving surgery followed by adjuvant radiotherapy is currently the therapeutic standard for patient with Breast Cancer. Symptoms are common among patients receiving this treatment. Ten percent of them will develop severe and chronic radio-induced toxicities, such as breast radio-induced-fibrosis impairing their quality of life (QoL). Yet, paying attention to symptom improves the empowerment and psychological adjustment to the disease. Web-based systems that can provide electronic-Patient reported Outcomes (e-PRO) have been shown to prompt clinicians to intensify symptom management, to improve symptom control, and to enhance patient-clinician communication patient satisfaction, as well as well-being.Benefits of systems to elicit e-PRO improve reliable measure of health-related quality of life (QoL) remains discussed. To date, there are few specific treatments for these severe radio-induced fibrosis except the antifibrotic combinaison Pentoxifylline/Vitamin E with inconsistent result. Since 2000, we and others have developed a mechanistic approach modulating the severity of RIF by targeting the Rho/ROCK/CTGF pathway, especially by inhibiting Rho activation by pravastatin. Our preclinical data, then followed by the Phase II PRAVACUR-01 trial, concluded that the use of pravastatin has an anti-fibrotic action on different experimental models and reduces the severity of the grade of fibrosis in 50% of patients. Patients can now benefit from this new anti-fibrotic agent. Taken as a whole, these data encourage combining both drug (pravastatin) and non-pharmacological intervention , in particular e-PRO, in the RIF management.

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Extracted eligibility criteria

Cancer type

Breast Carcinoma

Disease stage

Grade: at least grade 2 breast rif

Prior therapy

Must have received: conserving surgery

treated by conserving surgery

Must have received: radiation therapy — adjuvant

followed by adjuvant RT

Cannot have received: statin

Current treatment by : statin

Cannot have received: fibrate

Current treatment by : fibrate

Cannot have received: ciclosporin

Current treatment by : ciclosporin

Cannot have received: systemic fusidic acid

Current treatment by : systemic fusidic acid

Cannot have received: corticosteroid

Exception: long-term treatment

long-term treatment by corticoids

Cannot have received: systemic investigational drugs

Patients treated with systemic investigational drugs within the past 30 days

Lab requirements

Kidney function

serum creatinine ≤ 130 µmol/l

Liver function

asat and alat ≤ 2n; total bilirubin ≤ 1.5n

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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