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This issue of touchREVIEWS in Oncology & Haematology brings together a diverse collection of articles reflecting the growing complexity of cancer care and the continued evolution of precision medicine across tumour types. From rare malignancies and treatment-related challenges to emerging targeted therapies and novel biological insights, the contributions highlight both recent progress and the significant […]

touchMEETING HIGHLIGHTS

Enhancing personalized care in HR+ early breast cancer: How MGAs help to individualize risk-based systemic treatment decisions

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Video Chapters

Chair interview: enhancing personalized care in HR+ early breast cancer.

Learn more about HR+ early breast cancer care in an interview with Prof. Bianchini.
Prof. Giampaolo Bianchini
Duration: 17:15

Prognosis vs Prediction: does high-risk mean high response?

Prof. Paluch-Shimon discusses how to identify which patients with breast cancer are likely to benefit from chemotherapy.
Prof. Shani Paluch-Shimon
Duration: 13:48

Incorporating genomic testing when considering adjuvant CDK4/6 inhibitors.

Prof. Bianchini outlines perspectives for assessing CDK4/6 inhibitor eligibility and incorporating multi-gene assays to optimise therapy.
Prof. Giampaolo Bianchini
Duration: 15:20

Where are we with personalized approaches for node-positive patients? 

Dr. Reinisch explores the data driving personalized chemotherapy decisions in Germany, reflecting on the impact of menopausal status.
Dr. Mattea Reinisch
Duration: 14:53

Activity Overview

Faculty & Disclosures

Activity Overview
Faculty & Disclosures

The benefit of chemotherapy for adjuvant treatment of early HR+ breast cancer has historically been difficult to predict, as it is not fully predicted by traditional clinicopathologic factors alone, such as age, tumour size, grade, nodal status and ER expression.1,2 As a result, some patients may be overtreated and exposed to avoidable toxicity, while others may be undertreated.3 Guideline‑endorsed multi‑gene assays (MGAs), including the Oncotype DX 21‑gene recurrence score test, provide independent and complementary prognostic information beyond standard factors that may support clinicians in determining recurrence risk and estimating the likelihood of chemotherapy benefit.4,5 Current international and NCCN guidelines incorporate MGAs into decision algorithms, supporting more nuanced application of adjuvant chemotherapy.6,7 In addition, the emergence of adjuvant CDK4/6 inhibitors has expanded options for patients with higher residual risk of early breast cancer recurrence, including those with node‑positive disease.6–8

In this touchMEETING HIGHLIGHTS a leading panel of experts clarify early HR+ breast cancer prognosis versus prediction, illustrate how to incorporate genomic testing when considering adjuvant CDK4/6 inhibitors and outline current personalised approaches for patients with node‑positive disease.

  • Differentiate prognostic from predictive factors in breast cancer and explain the impact of high-risk disease on treatment response
  • Evaluate the role of genomic testing in guiding adjuvant CDK4/6 inhibitor decisions, including how results may support treatment selection in early HR+ breast cancer
  • Understand the personalised approach to managing patients with node-positive breast cancer, drawing upon data from clinical trials

For independent medical information from Exact Sciences is now Abbot Medical Affairs, please submit your question via this form.

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1

Early Breast Cancer Trialists’ Collaborative Group (EBCTCG), Peto R, Davies C, et al. Comparisons between different polychemotherapy regimens for early breast cancer: meta-analyses of long-term outcome among 100,000 women in 123 randomised trials. Lancet. 2012;379:432–444.

2

Sparano JA, Gray RJ, Makower DF, et al. Adjuvant Chemotherapy Guided by a 21-Gene Expression Assay in Breast Cancer. N Engl J Med. 2018;379:111–121.

3

Pak LM, Morrow M. Addressing the problem of overtreatment in breast cancer. Expert Rev Anticancer Ther. 2022;22:535–548.

4

Loibl S, André F, Bachelot T, et al. Early breast cancer: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up. Ann Oncol. 2024;35:159–182.

5

Andre F, Ismaila N, Allison KH, et al. Biomarkers for Adjuvant Endocrine and Chemotherapy in Early-Stage Breast Cancer: ASCO Guideline Update. J Clin Oncol. 2022;40:1816–1837.

6

NCCN Clinical Practice Guidelines in Oncology. Breast Cancer. Version 3. 2026. Available at: www.nccn.org (accessed June 2026).

7

Burstein HJ, Curigliano G, Gnant M, et al. Tailoring treatment to cancer risk and patient preference: the 2025 St Gallen International Breast Cancer Consensus Statement on individualizing therapy for patients with early breast cancer. Ann Oncol. 2025;36:1433–1446.

8

Curigliano G, et al. Updated treatment recommendations for systemic treatment: from the ESMO Metastatic Breast Cancer Living Guideline. Ann Oncol. 2025;36:1414–1418.

Prof. Giampaolo Bianchini

Vita-Salute San Raffaele University, Milan
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Prof. Giampaolo Bianchini

Vita-Salute San Raffaele University, Milan
Italy

Biography

Disclosures

Dr Mattea Reinisch

Prof. Shani Paluch-Shimon

Prof. Shani Paluch-Shimon

Hadassah-Hebrew University Medical Center, Jerusalem
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Prof. Shani Paluch-Shimon

Hadassah-Hebrew University Medical Center, Jerusalem
Israel

Biography

Disclosures

Prof. Giampaolo Bianchini

Dr Mattea Reinisch

Dr Mattea Reinisch

University Medical Centre Mannheim, Mannheim
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Dr Mattea Reinisch

University Medical Centre Mannheim, Mannheim
Germany

Biography

Disclosures

Prof. Shani Paluch-Shimon

Prof. Giampaolo Bianchini

Video Navigation

Video Chapters

Chair interview: enhancing personalized care in HR+ early breast cancer.

Learn more about HR+ early breast cancer care in an interview with Prof. Bianchini.
Prof. Giampaolo Bianchini
Duration: 17:15

Prognosis vs Prediction: does high-risk mean high response?

Prof. Paluch-Shimon discusses how to identify which patients with breast cancer are likely to benefit from chemotherapy.
Prof. Shani Paluch-Shimon
Duration: 13:48

Incorporating genomic testing when considering adjuvant CDK4/6 inhibitors.

Prof. Bianchini outlines perspectives for assessing CDK4/6 inhibitor eligibility and incorporating multi-gene assays to optimise therapy.
Prof. Giampaolo Bianchini
Duration: 15:20

Where are we with personalized approaches for node-positive patients? 

Dr. Reinisch explores the data driving personalized chemotherapy decisions in Germany, reflecting on the impact of menopausal status.
Dr. Mattea Reinisch
Duration: 14:53

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