The evolution of treatment strategies: aiming at the target
Phuong Dinh1, Christos Sotiriou, Martine J Piccart
1Department of Medical Oncology, Institut Jules Bordet, Université Libre de Bruxelles (U.L.B), 121 Blvd de Waterloo, 1000 Brussels, Belgium. phuong.dinh@bordet.be
Abstract:
Historically, the selection of adjuvant systemic therapy in early breast cancer has relied on risk assessment embodied by the TNM classification. Since the 2005 International St. Gallen Consensus, treatment selection now involves firstly identifying critical targets and then using risk to assess the trade-off between anticipated toxicity and efficacy. This evolution in treatment strategies began with the identification of the estrogen receptor, and culminated with the HER2 receptor, with recent astounding success in several adjuvant trials. Newer technologies including gene expression profiles and micrometastases tracking bear exciting potential in refining the treatment strategies further. Alongside the progress in developing agents that target different molecules across the whole breast cancer population, these newer technologies aim to tailor adjuvant treatment further by identifying breast cancer subgroups that may benefit most from being targeted with specific therapy, by defining molecular subtypes, recognizing chemo-sensitivity and resistance, identifying at-risk gene signatures, and by detecting stem cells capable of generating metastases. This paper will review this evolution of treatment strategies, from the lessons learnt from the past, to the exciting promise of tailored therapy of the future.
Insights
Adjuvant systemic therapy for early breast cancer is evolving from TNM classification to targeted treatments. Newer technologies like gene expression profiles promise more personalized therapies for better efficacy and reduced toxicity.
Area of Science:
- Oncology
- Translational Medicine
- Genomics
Background:
- Early breast cancer treatment historically relied on TNM staging.
- The 2005 International St. Gallen Consensus shifted focus to identifying critical molecular targets.
- Treatment selection now balances efficacy against toxicity, driven by receptor identification (estrogen, HER2).
Purpose of the Study:
- To review the evolution of adjuvant systemic therapy selection in early breast cancer.
- To highlight the transition from traditional risk assessment to targeted and personalized approaches.
- To discuss the potential of emerging technologies in refining treatment strategies.
Main Methods:
- Review of historical treatment selection criteria (TNM classification).
- Analysis of the impact of molecular target identification (estrogen receptor, HER2).
- Exploration of novel technologies: gene expression profiling, micrometastasis detection.
Main Results:
- Significant success in adjuvant trials using targeted therapies (e.g., HER2-targeted agents).
- Emerging technologies offer potential for further refinement of treatment strategies.
- Identification of molecular subtypes, chemo-sensitivity/resistance, and metastatic potential.
Conclusions:
- Adjuvant therapy for early breast cancer has significantly evolved towards personalized medicine.
- Gene expression profiles and other novel technologies are key to tailoring treatment.
- Future strategies aim to precisely match therapies to specific breast cancer subgroups for optimal outcomes.
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