# Challenges in managing recurrent luminal A breast cancer: a case study

**Authors:** Md Foorquan Hashmi, Fiza Khan, Elen Baloyan, Liana Safaryan, Davit Zohrabyan, Gevorg Tamamyan, Samvel Bardakhchyan

PMC · DOI: 10.3332/ecancer.2025.2048 · ecancermedicalscience · 2025-11-26

## TL;DR

A young woman with Luminal A breast cancer experienced rapid disease progression and death, highlighting the need for better treatment strategies for younger patients.

## Contribution

Highlights atypical aggressiveness of Luminal A breast cancer in young patients and calls for tailored treatment approaches.

## Key findings

- A 35-year-old patient with Luminal A breast cancer had multiple recurrences and died within 2 years.
- Younger patients with Luminal A breast cancer may have more aggressive disease than previously assumed.
- Current treatment approaches may be insufficient for younger individuals with this subtype.

## Abstract

Breast cancer, a leading cause of cancer-related mortality in women worldwide, exhibits diverse molecular subtypes with varying prognostic implications. Luminal A breast cancer, characterised by estrogen receptor positivity, progesterone receptor positivity and human epidermal growth factor receptor 2 negativity, typically has a favourable prognosis. However, we present a case of a 35-year-old female diagnosed with Luminal A breast cancer who experienced multiple recurrences and succumbed to the disease within 2 years of diagnosis. Despite initial treatment modalities, including surgery, chemotherapy and hormonal therapy, the patient faced relentless disease progression, highlighting the atypical clinical course observed in younger individuals with Luminal A breast cancer. This case underscores the discrepancy in prognosis between younger and older patients with Luminal A breast cancer, emphasising the need for tailored treatment approaches to address the challenges associated with disease recurrence and aggressiveness in younger populations. Further research is warranted to explain the underlying mechanisms driving the aggressive behaviour of Luminal A breast cancer in young patients and to develop targeted therapeutic strategies to improve outcomes in this population.

## Linked entities

- **Diseases:** breast cancer (MONDO:0004989), Luminal A breast cancer (MONDO:0021116)

## Full-text entities

- **Genes:** GNRH1 (gonadotropin releasing hormone 1) [NCBI Gene 2796] {aka GNRH, GRH, LHRH, LNRH}, SERPINE2 (serpin family E member 2) [NCBI Gene 5270] {aka GDN, GDNPF, PI-7, PI7, PN-1, PN1}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672] {aka BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675] {aka BRCC2, BROVCA2, FACD, FAD, FAD1, FANCD}, PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290] {aka CCM4, CLAPO, CLOVE, CWS5, HMH, MCAP}
- **Diseases:** Cancer (MESH:D009369), thrombocytopenia (MESH:D013921), coagulopathy (MESH:D001778), luminal A and B (MESH:D006509), invasive cancer (MESH:D009362), death (MESH:D003643), disease of hereditary angioedema (MESH:D030342), mastitis (MESH:D008413), obesity (MESH:D009765), Breast cancer (MESH:D001943), axillary lymphadenopathy (MESH:D008206), liver failure (MESH:D017093)
- **Chemicals:** Paclitaxel (MESH:D017239), Tamoxifen (MESH:D013629), Capecitabine (MESH:D000069287), Palbociclib (MESH:C500026), alpelisib (MESH:C585539), Epirubicin (MESH:D015251), CDK4/6 (-), capivasertib (MESH:C575618), Carboplatin (MESH:D016190), Fulvestrant (MESH:D000077267), alcohol (MESH:D000438), Cyclophosphamide (MESH:D003520), talazoparib (MESH:C586365), olaparib (MESH:C531550), Ribociclib (MESH:C000589651), Abemaciclib (MESH:C000590451)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]
- **Mutations:** E545K

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12950894/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950894/full.md

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Source: https://tomesphere.com/paper/PMC12950894