

Long-acting G-CSF empegfilgrastim with dose-dense chemotherapy for patients with stage II–III TNBC: Defendor Special trial, primary analysis
https://doi.org/10.33667/2078-5631-2025-14-53-59
Abstract
Triple-negative breast cancer (TNBC) remains one of the most aggressive subtypes of breast cancer, associated with a high risk of early recurrence and limited systemic treatment options. Despite advances in neoadjuvant therapy, including platinum-based agents and immune checkpoint inhibitors, the widespread adoption of these approaches is limited by their toxicity, cost, and insufficient data on their combination with dose-dense regimens.
Study objective. To evaluate the efficacy and safety of empegfilgrastim (a long-acting granulocyte colony-stimulating factor, G-CSF) in maintaining dose intensity during dose-dense neoadjuvant therapy (NAT) in patients with stage II–III triple-negative breast cancer (TNBC).
Materials and methods. This prospective study enrolled 60 patients who received dose-dense chemotherapy with the ddAC regimen (doxorubicin + cyclophosphamide every 14 days) followed by weekly paclitaxel and carboplatin. Empegfilgrastim was administered once after each ddAC cycle. The primary endpoint was achieving a relative dose intensity (RDI) of ≥ 85 %.
Results. The target RDI was achieved in 96 % of patients (median values: 100 % for ddAC and 94 % for weekly paclitaxel and carboplatin). Efficacy. A pathological complete response (pCR) was observed in 50 % of patients with localized (initially operable) disease and 43 % of those with locally advanced (initially inoperable) stages. Low residual tumor burden (RCB 0–1) was noted in 63 % of cases. Safety. The safety profile demonstrated a low incidence of severe adverse events (grade III–IV neutropenia: 1.7 %).
Conclusion. Empegfilgrastim effectively maintains high dose intensity in NAT, leading to a significant pCR rate comparable to that of immunotherapy but with a more favorable safety profile.
About the Authors
L. A. LokyanRussian Federation
Lusine A. Lokyan, resident oncologist
Moscow
I. P. Ganshina
Russian Federation
Inna P. Ganshina, PhD Med, leading researcher
Dept of Drug Treatment; Dept of Antitumor Drug Therapy No. 1
Moscow
I. V. Sorokina
Russian Federation
Irina V. Sorokina, PhD Med, global medical affairs lead
Moscow; Saint-Petersburg
E. V. Lubennikova
Russian Federation
Elena V. Lubennikova, PhD Med, senior researcher
Dept of Drug Treatment; Dept of Antitumor Drug Therapy No. 1
Moscow
S. G. Bagrova
Russian Federation
Svetlana G. Bagrova, PhD Med, senior researcher
Dept of Drug Treatment; Dept of Antitumor Drug Therapy No. 1
Moscow
L. G. Zhukova
Russian Federation
Liudmila G. Zhukova, DM Sci (habil.), RAS corresponding member, deputy director for Oncology
Moscow
D. A. Filonenko
Russian Federation
Daria A. Filonenko, PhD Med, head of Dept
Outpatient Chemotherapy Dept
Moscow
O. O. Gordeeva
Russian Federation
Olga O. Gordeeva, PhD Med, head of Dept
Outpatient Chemotherapy Dept
Moscow
K. S. Lezina
Russian Federation
Ksenia S. Lezina, resident oncologist
Moscow
E. V. Artamonova
Russian Federation
Elena V. Artamonova, DM Sci (habil.), head of Dept, professor
Dept of Chemotherapy No. 1; Dept of Oncology and Radiation Therapy; Dept of Oncology and Thoracic Surgery
Moscow
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Review
For citations:
Lokyan L.A., Ganshina I.P., Sorokina I.V., Lubennikova E.V., Bagrova S.G., Zhukova L.G., Filonenko D.A., Gordeeva O.O., Lezina K.S., Artamonova E.V. Long-acting G-CSF empegfilgrastim with dose-dense chemotherapy for patients with stage II–III TNBC: Defendor Special trial, primary analysis. Medical alphabet. 2025;(14):53-59. (In Russ.) https://doi.org/10.33667/2078-5631-2025-14-53-59