drugset / Trial / NCT05981014

Study of Autologous Tumor-Draining Lymph Node-Derived Lymphocytes as Neoadjuvant Therapy for HER2-Negative Breast Cancer

NCT05981014

RandomizedSequentialOpen-labelTreatment

Summary

RATIONALE: Patients with HER2-negative breast cancer not responding to initial neoadjuvant chemotherapy might have lower chances for a pathologic complete response (pCR) at definitive surgery, indicating worse prognosis. Adoptive cell therapy has demonstrated efficacy in advanced breast cancer, but whether the addition of adoptive cell therapy to neoadjuvant chemotherapy could increase the pCR rate remains unclear. Tumor-draining lymph node-derived lymphocytes (LNLs) that have abundant tumor-reactive T cells, but not exhausted T cells, are easy to produce. It is not yet known whether LNL treatment is safe and effective in patients with HER2-negative breast cancer not responding to neoadjuvant chemotherapy. PURPOSE: This open-label phase I/II trial is to investigate the safety and efficacy of autologous LNL in patients with HER2-negative breast cancer not responding to neoadjuvant chemotherapy.

Timeline

Start
2023-08-01
Primary completion
2030-12-31
Completion
2035-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Tumor-draining lymph node-derived lymphocyte Unknown 1e+09 cells
Subject Tumor-draining lymph node-derived lymphocyte Unknown 1.8e+10 cells
Background Cyclophosphamide Other / unclassified 60 mg/kg Intravenous
Background Cyclophosphamide Other / unclassified 600 mg/m2 Intravenous
Background Doxorubicin Other / unclassified 60 mg/m2 Intravenous
Background Epirubicin Small molecule 100 mg/m2 Intravenous
Background Fludarabine Small molecule 25 mg/m2 Intravenous
Background Paclitaxel Small molecule 260 mg/m2 Intravenous
Background aldesleukin Protein / enzyme biologic Intravenous

Indications