drugset / Trial / NCT06992336

Circulating Tumor DNA Guided Boost Therapy in Early Triple Negative Breast Patients With Residual Disease After Neoadjuvant Therapy

NCT06992336

RandomizedParallel-groupOpen-labelTreatment

Summary

Early triple negative breast cancer patients who do not achieve pathologic complete response after neoadjuvant chemotherapy with or without immunotherapy have bad prognosis. ctDNA effectively identified patients with highest relapse risk. This trial aims to explore whether the combination of anlotinib, immunotherapy and capecitabine could improve the outcome of this subgroup of high relapse risk patients compared with investigator's choice of therapy.

Timeline

Start
2025-04-10
Primary completion
2031-04-10
Completion
2036-01-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Benmelstobart Monoclonal antibody 200 mg Intravenous
Subject Catequentinib Small molecule 8 mg Oral
Background Capecitabine Small molecule 1000 mg/m2
Background Capecitabine Small molecule 1250 mg/m2

Indications