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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. Lokyan
N. N. Blokhin National Medical Investigation Centre of Oncology
Russian Federation

Lusine A. Lokyan, resident oncologist

Moscow



I. P. Ganshina
N. N. Blokhin National Medical Investigation Centre of Oncology
Russian Federation

Inna P. Ganshina, PhD Med, leading researcher

Dept of Drug Treatment; Dept of Antitumor Drug Therapy No. 1 

Moscow



I. V. Sorokina
A. S. Loginov Moscow Clinical Scientific and Practical Center of the Moscow Healthcare Department; JCS “BIOCAD”
Russian Federation

Irina V. Sorokina, PhD Med, global medical affairs lead

Moscow; Saint-Petersburg



E. V. Lubennikova
N. N. Blokhin National Medical Investigation Centre of Oncology
Russian Federation

Elena V. Lubennikova, PhD Med, senior researcher

Dept of Drug Treatment; Dept of Antitumor Drug Therapy No. 1

Moscow



S. G. Bagrova
N. N. Blokhin National Medical Investigation Centre of Oncology
Russian Federation

Svetlana G. Bagrova, PhD Med, senior researcher

Dept of Drug Treatment; Dept of Antitumor Drug Therapy No. 1

Moscow



L. G. Zhukova
A. S. Loginov Moscow Clinical Scientific and Practical Center of the Moscow Healthcare Department
Russian Federation

Liudmila G. Zhukova, DM Sci (habil.), RAS corresponding member, deputy director for Oncology

Moscow



D. A. Filonenko
A. S. Loginov Moscow Clinical Scientific and Practical Center of the Moscow Healthcare Department
Russian Federation

Daria A. Filonenko, PhD Med, head of Dept

Outpatient Chemotherapy Dept

Moscow



O. O. Gordeeva
Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency
Russian Federation

Olga O. Gordeeva, PhD Med, head of Dept

Outpatient Chemotherapy Dept

Moscow



K. S. Lezina
N. N. Blokhin National Medical Investigation Centre of Oncology
Russian Federation

Ksenia S. Lezina, resident oncologist

Moscow



E. V. Artamonova
N. N. Blokhin National Medical Investigation Centre of Oncology; N. I. Pirogov Russian National Research Medical University; M. F. Vladimirsky Moscow Regional Research and Clinical Institute (MONIKI)
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



References

1. Shimelis H, LaDuca H, Hu C, Hart SN, Na J, Thomas A, Akinhanmi M, Moore RM, Brauch H, Cox A, Eccles DM, Ewart-Toland A, Fasching PA, Fostira F, Garber J, Godwin AK, Konstantopoulou I, Nevanlinna H, Sharma P, Yannoukakos D, Yao S, Feng BJ, Tippin Davis B, Lilyquist J, Pesaran T, Goldgar DE, Polley EC, Dolinsky JS, Couch FJ. Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing. J Natl Cancer Inst. 2018 Aug 1; 110 (8): 855–862. DOI: 10.1093/jnci/djy106. PMID: 30099541; PMCID: PMC 6093350.

2. Artamonova E.V., Kovalenko E. I. Systemic Treatment of Breast Cancer. 2<sup>nd</sup> ed., rev. and exp., Re Media Advertising Agency, 2021. (In Russ.).

3. Zhukova L.G. (2015). Breast cancer with triple-negative phenotype in the Russian population of patients. Clinical-morphological features. Problems in Oncology. 2015; 61 (2): 189–194. – EDN: TRUXAP. (In Russ.).

4. Poggio F, Tagliamento M, Ceppi M, Bruzzone M, Conte B, Fregatti P, Punie K, de Azambuja E, Del Mastro L, Lambertini M. Adding a platinum agent to neoadjuvant chemotherapy for triple-negative breast cancer: the end of the debate. Ann Oncol. 2022 Mar; 33 (3): 347–349. DOI: 10.1016/j.annonc.2021.11.016. Epub 2021 Nov 30. PMID: 34861375.

5. Wolmark N, Wang J, Mamounas E, Bryant J, Fisher B. Preoperative chemotherapy in patients with operable breast cancer: nine-year results from National Surgical Adjuvant Breast and Bowel Project B-18. J Natl Cancer Inst Monogr. 2001; (30): 96–102. DOI: 10.1093/oxfordjournals.jncimonographs.a003469. PMID: 11773300.

6. Korde LA, Somerfield MR, Carey LA, Crews JR, Denduluri N, Hwang ES, Khan SA, Loibl S, Morris EA, Perez A, Regan MM, Spears PA, Sudheendra PK, Symmans WF, Yung RL, Harvey BE, Hershman DL. Neoadjuvant Chemotherapy, Endocrine Therapy, and Targeted Therapy for Breast Cancer: ASCO Guideline. J Clin Oncol. 2021 May 1; 39 (13): 1485–1505. DOI: 10.1200/JCO.20.03399. Epub 2021 Jan 28. PMID: 33507815; PMCID: PMC 8274745.

7. Loibl S, O’Shaughnessy J, Untch M, Sikov WM, Rugo HS, McKee MD, Huober J, Golshan M, von Minckwitz G, Maag D, Sullivan D, Wolmark N, McIntyre K, Ponce Lorenzo JJ, Metzger Filho O, Rastogi P, Symmans WF, Liu X, Geyer CE Jr. Addition of the PARP inhibitor veliparib plus carboplatin or carboplatin alone to standard neoadjuvant chemotherapy in triple-negative breast cancer (BrighTNess): a randomised, phase 3 trial. Lancet Oncol. 2018 Apr; 19 (4): 497–509. DOI: 10.1016/S1470-2045(18)30111-6. Epub 2018 Feb 28. PMID: 29501363.

8. Schmid P, Cortes J, Pusztai L, McArthur H, Kümmel S, Bergh J, Denkert C, Park YH, Hui R, Harbeck N, Takahashi M, Foukakis T, Fasching PA, Cardoso F, Untch M, Jia L, Karantza V, Zhao J, Aktan G, Dent R, O’Shaughnessy J; KEYNOTE-522 Investigators. Pembrolizumab for Early Triple-Negative Breast Cancer. N Engl J Med. 2020 Feb 27; 382 (9): 810–821. DOI: 10.1056/NEJMoa1910549. PMID: 32101663.

9. Early Breast Cancer Trialists’ Collaborative Group (EBCTCG). Increasing the dose intensity of chemotherapy by more frequent administration or sequential scheduling: a patient-level meta-analysis of 37 298 women with early breast cancer in 26 randomised trials. Lancet. 2019 Apr 6; 393 (10179): 1440–1452. DOI: 10.1016/S0140-6736(18)33137-4. Epub 2019 Feb 8. PMID: 30739743; PMCID: PMC 6451189.

10. Kovalenko E. I., Zhulikov Ya.A., Artamonova E. V., Khoroshilov M. V., Petrovskiy A. V., Denchik D. A., Drujinina D. I., Vorotnikov I. K. Dose-dense neoadjuvant chemotherapy of operable and locally advanced inoperable triple negative breast cancer: First results of single-centre prospective trial. Medical alphabet. 2023; (10): 11–17. (In Russ.).

11. Gordeeva O. O., Kolyadina I. V., Zhukova L. G., Gan’shina I.P., Komov D. V., Meshcheriakov A. A. The efficacy of neoadjuvant chemotherapy and survival in older patients with stages II to III triple-negative breast cancer. Journal of Modern Oncology. 2019; 21 (3): 46–51. (In Russ.).

12. Common Terminology Criteria for Adverse Events (CTCAE) v5.0.

13. Cornes P. et al. Systematic Review and Meta-analysis of Short- versus Long-Acting Granulocyte Colony-Stimulating Factors for Reduction of Chemotherapy-Induced Febrile Neutropenia. Adv Ther. 2018 Nov; 35 (11):1816–1829. DOI: 10.1007/s12325-018-0798-6

14. Bagrova S. G. Granulocyte colony-stimulating factors in the prevention of febrile neutropenia. Effective pharmacotherapy. 2015; (31): 6–15. (In Russ.).

15. Krivorotko P. V., Burdaeva O. N., Nechaeva M. N. et al. Efficacy and safety of Extimia® (empegfilgrastim): results of a double-blind controlled phase III study in patients with diagnosis «breast cancer» receiving myelosuppressive chemotherapy. Journal of Modern Oncology. 2015; 17 (2): 45–52. (In Russ).


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

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ISSN 2078-5631 (Print)
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