Evidence map›Paper›PMID 42428078›Full record

ArticlemedRxiv : the preprint server for health sciences2026

The MHCII Immune Activation Score predicts risk of recurrence and benefit of taxanes in Basallike and HER2-enriched breast cancer.

Philip S Bernard, Bingshu E Chen, Dongxia Gao, Lois E Shepherd, Torsten O Nielsen, Katherine E Varley

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In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Philip S BernardDepartment of Pathology, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Bingshu E ChenCanadian Cancer Trials Group, Queen's University, Kingston, ON, Canada.
Dongxia GaoDepartment of Pathology and Laboratory Medicine, BC Cancer and University of British Columbia, Vancouver, Canada.
Lois E ShepherdCanadian Cancer Trials Group, Queen's University, Kingston, ON, Canada.
Torsten O NielsenDepartment of Pathology and Laboratory Medicine, BC Cancer and University of British Columbia, Vancouver, Canada.
Katherine E VarleyDepartment of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.

Funding

Validation of the MHC II Immune Activation Assay in Breast CancerUH3CA262221 · NCI · UNIVERSITY OF UTAH · PI BERNARD, PHILIP S, VARLEY, KATHERINE ELENA · 2022 to 2024
$1.0M
NCI NIH HHS UH3 CA262221
6 · The paper itself

Abstract

Purpose: There are no clinically validated biomarkers to assess recurrence risk and guide treatment de-escalation in Basal-like and HER2-enriched breast cancer. Taxane-based chemotherapy remains a cornerstone of treatment despite significant toxicity. We evaluated the prognostic and predictive utility of the MHCII Immune Activation Score (IA Score) in these subtypes. Experimental Design: We retrospectively analyzed Basal-like and HER2-enriched breast cancers from the NCIC CTG MA.21 trial, which randomized patients with node-positive or high-risk node-negative disease to adjuvant chemotherapy with or without taxanes. MA.21 predated immune checkpoint inhibitors and routine HER2-targeted therapy. Subtype was previously assigned by PAM50. The 36-gene MHCII-IA assay used RNA from formalin-fixed, paraffin-embedded tissue. Multivariable Cox and Kaplan-Meier analyses evaluated associations between IA Score, clinicopathologic variables, tumor-infiltrating lymphocytes (TILs), relapse-free survival (RFS), and taxane benefit. Results: Among Basal-like (N=317) and HER2-enriched (N=155) tumors, higher IA Score was associated with improved RFS independent of lymph node status and provided stronger prognostic discrimination than TILs. Node-negative patients with high IA Score had excellent outcomes (8-year RFS >90%) versus those with low IA Score (8-year RFS <76%). In node-positive disease, high IA Score increased 8-year RFS by >10% relative to low IA Score. IA Score stratified taxane benefit: node-positive IA-low patients benefited, whereas IA-high tumors had favorable outcomes regardless of regimen. Conclusions: MHCII Immune Activation Score is a prognostic and predictive biomarker in Basal-like and HER2-enriched breast cancer. High IA Score identified patients with excellent outcomes before pembrolizumab, trastuzumab, and taxane-based treatment escalation, providing a rationale for prospective risk-adapted de-escalation strategies.

Identifiers

PMID42428078
PMCPMC13345503

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.