Also considered

๐ŸŒธ Breast Cancer โ€” 2026-W38

12 papers judged, 3 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

Risk-Adapted Optimization of Neoadjuvant Therapy in Human Epidermal Growth Factor Receptor 2-Positive Early-Stage Breast Cancer.
Emailed
Kleeman Sam O et al., J Clin Oncol

Narrative review in JCO on optimizing neoadjuvant/postneoadjuvant therapy for HER2+ early breast cancer, including de-escalation strategies and new agents like trastuzumab deruxtecan. Offers a practical framework for risk-adapted, biomarker-guided treatment selection in this setting.

Neoadjuvant Pertuzumab Biosimilar HLX11 Versus Reference Pertuzumab for Early-stage or Locally Advanced Breast Cancer: A phase 3 Equivalence Trial.
Emailed
Zhang Jin et al., Clin Cancer Res

Phase 3 randomized equivalence trial comparing a pertuzumab biosimilar to reference pertuzumab in neoadjuvant HER2-positive breast cancer, published in Clinical Cancer Research. Demonstrates biosimilarity in pathologic response, safety, and pharmacokinetics, supporting the biosimilar as an interchangeable treatment option.

Trastuzumab Botidotin Versus Trastuzumab Emtansine in Human Epidermal Growth Factor Receptor 2-Positive Advanced Breast Cancer: A Phase III, Open-Label, Randomized Controlled Trial.
Emailed
Zhang Jian et al., J Clin Oncol

Phase 3 randomized trial in HER2-positive metastatic breast cancer previously treated with trastuzumab and a taxane, published in JCO. A novel HER2-directed antibody-drug conjugate improved progression-free survival over trastuzumab emtansine, supporting it as a potential new standard second-line option.

Treatment Effect Discrepancy Between PFS and OS in Antibody-Drug Conjugate Trials for Metastatic Breast Cancer: A Meta-Epidemiologic Analysis.
Website only
Costa de Almeida Luiz Felipe et al., J Natl Cancer Inst

Meta-epidemiologic analysis of randomized trials of antibody-drug conjugates in metastatic breast cancer, published in JNCI. Finds that PFS effects consistently overstate OS effects, informing how oncologists interpret PFS-based ADC trial results and regulatory decisions.

Safety and antitumor activity of the first-in-class EGFR-HER3 bispecific antibody-drug conjugate iza-bren (BL-B01D1) in patients with pretreated locally advanced or metastatic breast cancer: a phase 1b study.
Website only
Zhang J et al., Ann Oncol

Phase 1b study of the novel EGFR-HER3 bispecific antibody-drug conjugate iza-bren in heavily pretreated metastatic breast cancer (HER2+, HR+/HER2-, and triple-negative), published in Annals of Oncology. Shows clinically meaningful and durable objective responses across subtypes, signaling a promising new ADC option pending further trials.

ERBB2 Activating Mutations Promote Enhanced Internalization and Activity of Trastuzumab Deruxtecan in HER2-non-amplified Metastatic Breast Cancer.
Website only
Mai Nicholas et al., Clin Cancer Res

Retrospective translational study in Clinical Cancer Research examining ERBB2 activating mutations as a predictor of response to trastuzumab deruxtecan in HER2-non-amplified metastatic breast cancer, with supporting preclinical mechanistic data. Suggests these mutations could help identify patients likely to benefit more from T-DXd.

Epigenetic plus cytokine therapy induces stem-like CD8+ T-cell reservoirs and intratumoral immune niches to overcome anti-PD-1 resistance.
Not selected
Minnar Christine Mall et al., J Immunother Cancer

Preclinical translational study (J Immunother Cancer) combining epigenetic and cytokine therapy with anti-PD-1 in checkpoint-resistant murine colorectal and breast cancer models, identifying an immune-niche gene signature associated with favorable clinical response to checkpoint blockade in patient genomic datasets. Suggests a rational combination strategy and biomarker to overcome anti-PD-1 resistance, though still early-stage evidence.

Endocrine Biomarker Changes in a Randomised Low-Dose Tamoxifen Trial for Breast Cancer Prevention.
Not selected
Nash Stephen et al., J Natl Cancer Inst

Randomized, placebo-controlled dose-finding trial (KARISMA) in healthy women examining endocrine biomarker changes across low-dose tamoxifen regimens, published in JNCI. Provides mechanistic support for lower-dose tamoxifen in breast cancer prevention but reports only surrogate endocrine markers, not cancer outcomes.

(Neo)adjuvant approvals for solid tumors by the US Food and Drug Administration 2010-2023.
Not selected
Valiente Consolacion Molto et al., J Natl Cancer Inst

Descriptive analysis of FDA (neo)adjuvant drug approvals for solid tumors (2010-2023), published in JNCI, spanning melanoma, breast, and lung cancer trials. Highlights inconsistencies in trial design, endpoint reporting, and quality-of-life data that inform how oncologists interpret the evidence behind approved (neo)adjuvant regimens.

Association of immune and proliferation gene signatures and stromal tumor-infiltrating lymphocytes with clinical outcomes in patients with stage I triple-negative breast cancer.
Not selected
Tarantino Paolo et al., Eur J Cancer

Retrospective cohort study in stage I triple-negative breast cancer published in European Journal of Cancer, evaluating a gene-expression assay and stromal TILs as prognostic biomarkers. Findings suggest potential to identify very-low-risk subsets, but the markers were not predictive of therapy response and did not significantly stratify recurrence risk overall.

Integrating genetic predictors into subsequent breast cancer risk prediction in survivors of childhood cancer.
Not selected
Srinivasan Aparna et al., J Natl Cancer Inst

Translational cohort study in JNCI examining polygenic risk scores and pathogenic variants for predicting subsequent breast cancer risk in childhood cancer survivors. Informs risk stratification and surveillance rather than therapy selection, so it refines screening discussions rather than treatment decisions.

Evaluation of a Tumor-Informed Molecular Residual Disease Assay in Early Triple-Negative Breast Cancer Treated With Neoadjuvant Chemotherapy, With or Without Atezolizumab.
Not selected
Balic Marija et al., JCO Precis Oncol

Prospective ctDNA substudy of a phase 3 trial (NSABP B-59) in stage II/III triple-negative breast cancer treated with neoadjuvant chemotherapy with or without atezolizumab, published in JCO Precision Oncology. Shows ctDNA clearance after therapy correlates with distant recurrence risk, supporting its potential use as a prognostic tool in early TNBC.

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