# Optimizing second-line endocrine-based treatment in HR positive HER2 negative metastatic breast cancer: a comprehensive expert statement from the Gulf Cooperation Council Region

**Authors:** Ahmed Alshehri, Abdullah Khalaf Altwairgi, Abdulwahab AlTourah, Ahmed Alwbari, Aref Chehal, Francois Calaud, Hashem Al-Hashem, Husam Marashi, Sherif Elsamany, Syed Hammad Tirmazy

PMC · DOI: 10.3389/fonc.2025.1706670 · 2026-01-22

## TL;DR

This paper provides expert guidance for optimizing second-line treatment of a specific type of breast cancer in the Gulf Cooperation Council region, considering local healthcare challenges and patient needs.

## Contribution

The paper offers region-specific, pragmatic recommendations for HR+/HER2-negative metastatic breast cancer treatment in the GCC, adapted to local constraints.

## Key findings

- Early genomic testing for PIK3CA, AKT, BRCA, and ESR1 is recommended to guide therapy.
- Oral SERDs and PI3K/AKT inhibitors are prioritized in second-line treatment strategies.
- Alpelisib should be used cautiously in diabetic patients, and shared decision-making is emphasized.

## Abstract

Optimizing second-line therapy for hormone receptor-positive (HR+) and human epidermal growth factor receptor 2–negative (HER2-negative) metastatic breast cancer (mBC) in the Gulf Cooperation Council (GCC) is challenged by variations in diagnostic capacity, drug accessibility, comorbidities, and treatment pathways compared with other regions. While international guidelines provide an overarching evidence framework for breast cancer management, their practical application at the regional level often requires adaptation to local healthcare resources. There is an unmet need to optimize the treatment sequencing strategies for patients with HR+/HER2-negative mBC in the GCC region through expert guidance. Given this context, a virtual advisory board involving 10 oncologists from the GCC region was convened in November 2024. The panel aimed to review current evidence and develop pragmatic, implementable recommendations for second-line management. This consensus uniquely contextualizes global evidence for GCC-specific healthcare constraints, addressing gaps in diagnostic access, affordability, and real-world feasibility, while providing treatment recommendations that help clinicians refine therapeutic strategies and incorporate patient preferences for improved outcomes. The panel recommends early genomic testing (PIK3CA, AKT, BRCA, ESR1) to guide therapy, prioritizing targeted agents such as oral SERDs and PI3K/AKT inhibitors in second-line sequencing, cautious use of alpelisib in diabetic patients, and incorporating patient preferences through shared decision-making and multidisciplinary care.

## Linked entities

- **Genes:** PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], Brca2 (BRCA2, DNA repair associated) [NCBI Gene 37916], ESR1 (estrogen receptor 1) [NCBI Gene 2099]
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290] {aka CCM4, CLAPO, CLOVE, CWS5, HMH, MCAP}, BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672] {aka BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}
- **Diseases:** breast cancer (MESH:D001943), diabetic (MESH:D003920)
- **Chemicals:** SERDs (-), alpelisib (MESH:C585539)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12872529/full.md

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Source: https://tomesphere.com/paper/PMC12872529