drugset / Trial / NCT02978495

Neoadjuvant Carboplatin in Triple Negative Breast Cancer

NCT02978495 ↗

Phase 2 Completed 154 enrolled Barretos Cancer Hospital
RandomizedParallel-groupOpen-labelTreatment

Summary

Breast cancer is the most frequent neoplasm in women in Brazil and in the world and up to 15% of all cases diagnosed correspond to the triple negative subtype. Triple negative breast cancer affects young women with germline mutations in BRCA 1/2 genes. Giving the lack of target therapies to date, there is no consensus regarding the most effective treatment for this subgroup of tumors. Although evidence shows that triple negative breast cancer is highly sensitive to chemotherapy when compared to other breast tumors, there is no evidence to support the hypothesis that patients with triple negative breast cancer and mutation in BRCA1 / 2 genes have higher chemosensitivity to neoadjuvant therapy. The investigator proposes a prospective, randomized, open-label, phase II study, evaluating the rate of complete pathologic response, disease-free survival, overall survival and prognostic evaluation of BRCA1 / 2 mutation status in women with triple negative breast cancer submitted to sequential neoadjuvant chemotherapy based on anthracycline and taxane, with or without carboplatin.

Timeline

Start
2017-05-17
Primary completion
2019-12-02
Completion
2021-10-22

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboplatin Small molecule 1.5 unknown —
Background Cyclophosphamide Other / unclassified 600 mg/m2 —
Background Doxorubicin Other / unclassified 60 mg/m2 —
Background Paclitaxel Small molecule 80 mg/m2 —