Submit manuscript...
Journal of
eISSN: 2373-633X

Cancer Prevention & Current Research

Research Article Volume 17 Issue 1

Adjuvant systemic therapy in early breast cancer: from CMF to precision risk-adapted treatment

Adrian Hunis MD

Emeritus member of ASCO, ESMO, Honorary member of AMA, Argentina

Received: March 02, 2026 | Published: March 11, 2026

Citation: Hunis A. Adjuvant systemic therapy in early breast cancer: from CMF to precision risk-adapted treatment. J Cancer Prev Curr Res. 2026;17(1):9‒13. DOI: 10.15406/jcpcr.2026.17.00599

Download PDF

Abstract

Background: Adjuvant systemic therapy has fundamentally altered the natural history of early breast cancer. Beginning with Bonadonna’s CMF program, the curative principle of micrometastatic eradication became clinically proven, and subsequent EBCTCG meta-analyses quantified durable reductions in recurrence and mortality with polychemotherapy.1–6

Methods: Evidence-based narrative review of biological foundations (tumor kinetics and resistance), landmark randomized trials, meta-analyses, and contemporary subtype-driven strategies integrating chemotherapy, endocrine therapy, and modern biologic/targeted agents.

Results: Anthracycline and taxane-based regimens improved outcomes over earlier approaches, with additional gains from dose-dense scheduling (validated by randomized trials). HER2-directed therapy (trastuzumab ± pertuzumab) produced major reductions in recurrence; response-adapted escalation with antibody–drug conjugates further improved outcomes in residual disease. In HR-positive disease, endocrine therapy is foundational and long-horizon, while genomic assays refine chemotherapy selection. In TNBC, post-neoadjuvant capecitabine and perioperative immunotherapy improve event-free outcomes. In selected high-risk HR+/HER2− disease, CDK4/6 inhibition improves invasive disease-free survival; and in germline BRCA1/2-mutated high-risk HER2− disease, adjuvant PARP inhibition improves invasive DFS and overall survival.4–12,14–30

Conclusions: Modern adjuvant care is biology-driven and risk-adapted. Integrating subtype, nodal burden, genomic risk, and response to preoperative therapy maximizes cure while minimizing toxicity and overtreatment. Future directions include ctDNA-based minimal residual disease (MRD) strategies and adaptive escalation/de-escalation trials.31–36

 

Keywords: systemic therapy, contemporary,cancer mortality

Creative Commons Attribution License

©2026 Hunis. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.