Also considered

๐ŸŒธ Breast Cancer โ€” 2026-W39

4 papers judged, 1 emailed  ยท  Read the digest →

What this page is. Every paper the week's monitor reviewed โ€” including the ones that did not go into the digest. Material marked “Not selected” was reviewed and deliberately left out. It has not been fact-checked to digest standard and is not endorsed. For the curated read, see the digest itself.

Papers judged this week

Navigating uncertainties and evidence gaps in adjuvant therapy for premenopausal women with HR+/HER2- breast cancer.
Emailed
Licata L et al., Ann Oncol

Narrative review in Ann Oncol addressing evidence gaps in adjuvant therapy for premenopausal HR+/HER2- early breast cancer, covering ovarian suppression, genomic assay use, extended endocrine therapy, and survivorship issues. Offers a practical framework to individualize adjuvant treatment decisions in this distinct population.

Efficacy, safety and circulating tumor cell dynamics in patients treated with Eribulin for HER2-negative advanced breast cancer - results from the phase II DETECT IVb trial.
Website only
Schochter F et al., Breast Cancer Res Treat

Single-arm phase 2 trial in HER2-negative metastatic breast cancer treated with eribulin, published in Breast Cancer Research and Treatment. Confirms eribulin's efficacy and shows circulating tumor cell clearance correlates with progression-free survival, offering a potential on-treatment monitoring tool.

E7389-LF as a first-line chemotherapy for patients with metastatic/advanced HER2-negative breast cancer: results from the phase 1 dose-expansion part of study 114.
Not selected
Ishiguro Hiroshi et al., Breast Cancer Res

Phase 1 dose-expansion study of first-line E7389-LF chemotherapy in metastatic HER2-negative breast cancer, published in Breast Cancer Research. Shows a meaningful objective response rate and PFS in an unmet first-line population, supporting further development of this agent.

70-gene signature MammaPrint for early-stage HR-positive, HER2-negative breast cancer: Outcome in the MINDACT trial for key clinical-pathological high-risk subgroups.
Not selected
Gielen Robbert C A M et al., Eur J Cancer

Exploratory subgroup analysis of the MINDACT phase III trial evaluating the 70-gene MammaPrint signature in clinically high-risk, genomically low-risk HR+/HER2- early breast cancer, published in Eur J Cancer. Reinforces that adjuvant chemotherapy adds little benefit even in higher clinical-risk subgroups when genomic risk is low, supporting continued use of the assay for chemotherapy de-escalation decisions.

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