Evidence map›Paper›PMID 39192887›Full record

ArticleBreast cancer (Dove Medical Press)2024

Comprehensive Assessment of Immune Phenotype and Its Effects on Survival Outcomes in HER2-Low versus HER2-Zero Breast Cancer.

Heidi Chwan Ko, R J Seager, Sarabjot Pabla, Maria-Fernanda Senosain, Erik Van Roey, Shuang Gao, Kyle C Strickland, Rebecca Ann Previs, Michelle F Green, Maureen Cooper and 11 more

Abstract read
In one paragraph

Article in Breast cancer (Dove Medical Press), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Heidi Chwan Ko *Labcorp Oncology, Durham, NC, USA.ORCID 0000-0002-7247-9175
R J Seager *Labcorp Oncology, Buffalo, NY, USA.ORCID 0000-0002-2866-5288
Sarabjot PablaLabcorp Oncology, Buffalo, NY, USA.
Maria-Fernanda SenosainLabcorp Oncology, Buffalo, NY, USA.ORCID 0000-0002-3933-7167
Erik Van RoeyLabcorp Oncology, Buffalo, NY, USA.
Shuang GaoLabcorp Oncology, Buffalo, NY, USA.
Kyle C StricklandLabcorp Oncology, Durham, NC, USA.
Rebecca Ann PrevisLabcorp Oncology, Durham, NC, USA.
Michelle F GreenLabcorp Oncology, Durham, NC, USA.
Maureen CooperLabcorp Oncology, Durham, NC, USA.
Mary K NeslineLabcorp Oncology, Durham, NC, USA.
Stephanie B HastingsLabcorp Oncology, Durham, NC, USA.
Kobina Agyaful AmoahLabcorp Oncology, Durham, NC, USA.ORCID 0009-0000-2217-0244
Shengle ZhangLabcorp Oncology, Buffalo, NY, USA.
Jeffrey M ConroyLabcorp Oncology, Buffalo, NY, USA.
Taylor J JensenLabcorp Oncology, Durham, NC, USA.
Marcia EisenbergLabcorp, Burlington, NC, USA.
Brian CaveneyLabcorp, Burlington, NC, USA.
Eric A SeversonLabcorp Oncology, Durham, NC, USA.
Shakti RamkissoonLabcorp Oncology, Durham, NC, USA.
Shipra GandhiDepartment of Hematology and Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The understanding of molecular characteristics of HER2-low breast cancer is evolving since the establishment of trastuzumab deruxtecan. Here, we explore the differences in expression patterns of immune-related genes in the tumor immune microenvironment (TME) and survival between HER2-low and HER2-zero breast cancers. Methods: Comprehensive genomic and immune profiling, including RNA-seq gene expression assessment of 395 immune genes, was performed on FFPE samples from 129 patients with advanced HER2-negative (immunohistochemistry (IHC) 0, 1+ or 2+ with negative Results: There were no significant differences in mRNA expressions of immune-related genes between HER2-low and HER2-zero breast cancers. However, HER2-low breast cancers were associated with a higher proportion of ER-positivity. When ER was analyzed along with HER2, we observed a significantly higher tumor immunogenic signature (TIGS) expression in HER2-zero/ER-negative tumors than in HER2-low/ER-positive tumors (p=0.0088). Similarly, lower expression of PD-L1 and T cell immunoglobulin and ITIM domain (TIGIT) mRNA was observed in HER2-low/ER-positive tumors when compared to HER2-zero/ER-negative tumors (p=0.014 and 0.012, respectively). Patients with HER2-low tumors had a longer median OS than those with HER2-zero tumors (94 months vs 42 months, p=0.0044). Conclusion: Patients with HER2-low breast cancer have longer survivals yet display no differences in immune-related gene expression when compared to those with HER2-zero cancers. The differences in survival can be attributed to the higher rate of ER-positivity seen in HER2-low breast cancers, compared to HER2-zero tumors.

Indexed as

estrogen receptorgene expression profilingHER2-low breast cancerimmune checkpoint biomarkersimmune profilingtumor immune microenvironment

Identifiers

PMID39192887
PMCPMC11348991

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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.