# Exceptional Response to Pembrolizumab in Metastatic ER+/HER2− Breast Cancer With Liver Metastases: A Case Report and Literature Review

**Authors:** Claudia Villa Celi, Supriya Peshin, Adit Dharia, Faizan Bashir, Linden Erica

PMC · DOI: 10.1155/crom/7970572 · Case Reports in Oncological Medicine · 2025-10-14

## TL;DR

A patient with hormone receptor-positive breast cancer showed a strong response to pembrolizumab after developing high PD-L1 expression in liver metastases.

## Contribution

Demonstrates exceptional response to immunotherapy in a typically resistant breast cancer subtype with high PD-L1 expression.

## Key findings

- The patient achieved near-complete remission with pembrolizumab after progressing on other therapies.
- High PD-L1 expression (CPS 95%) was observed in liver metastases, which correlated with treatment response.
- The remission lasted about 10 months before disease progression.

## Abstract

Hormone receptor–positive (HR+) and HER2-negative breast cancer is the most common subtype in women, particularly in the postmenopausal setting. Unlike triple-negative breast cancer, the benefit of immune checkpoint inhibitors (ICIs) in HR+/HER2− disease remains uncertain because of low tumor immunogenicity and limited PD-L1 expression.

We describe a case of a 70-year-old woman who presented with severe anemia and was incidentally found to have a bleeding left breast mass. Biopsy confirmed Grade 3 invasive ductal carcinoma (ER+/PR+ > 95%, HER2−) with nodal involvement but no distant metastases, consistent with Stage IIIc disease. She was treated with neoadjuvant anastrozole, modified radical mastectomy, adjuvant chemotherapy, radiation, and continued endocrine therapy. After 3 years, she developed extensive hepatic metastases. Biopsy revealed ER+/PR−/HER2− disease with striking PD-L1 expression (CPS 95%). The disease progressed on fulvestrant and palbociclib, but switching to carboplatin, gemcitabine, and pembrolizumab led to rapid improvement: liver function normalized and imaging showed near-complete response within 3 months. This remission lasted about 10 months before disease progression and transition to hospice care.

This case explains the potential role of ICIs in HR+/HER2− breast cancer with unusually high PD-L1 expression. It underscores the importance of biomarker-driven treatment and supports expanding PD-L1 testing to better identify patients who may benefit from immunotherapy in this traditionally resistant subtype.

## Linked entities

- **Proteins:** CD274 (CD274 molecule)
- **Chemicals:** anastrozole (PubChem CID 2187), fulvestrant (PubChem CID 104741), palbociclib (PubChem CID 5330286), carboplatin (PubChem CID 426756), gemcitabine (PubChem CID 60750)
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** nodal (MESH:D013611), triple-negative breast cancer (MESH:D064726), Stage IIIc disease (MESH:C565553), anemia (MESH:D000740), bleeding left breast mass (MESH:D061325), invasive ductal carcinoma (MESH:D044584), Liver Metastases (MESH:D009362), Breast Cancer (MESH:D001943), tumor (MESH:D009369)
- **Chemicals:** Pembrolizumab (MESH:C582435), carboplatin (MESH:D016190), fulvestrant (MESH:D000077267), anastrozole (MESH:D000077384), gemcitabine (MESH:D000093542), palbociclib (MESH:C500026)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12539981/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12539981/full.md

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Source: https://tomesphere.com/paper/PMC12539981