# Unlocking the Potential of Rucaparib: A Case Series on Its Impact in Metastatic Breast Cancer With Mutations

**Authors:** Chandrakanth MV, Vivek Agarwala, Neha Choudhary, Amit Sharma, Minakshi Roy, Kaustav Mandal, Moinak Basu, Nibedita Sen, Pritam K Sarkar, Subhabrata Kumar

PMC · DOI: 10.7759/cureus.60963 · Cureus · 2024-05-23

## TL;DR

This case series shows that rucaparib is effective in treating metastatic breast cancer in patients with BRCA1/2 mutations.

## Contribution

The study provides new evidence on rucaparib's efficacy in metastatic breast cancer with both germline and somatic BRCA mutations.

## Key findings

- Rucaparib led to a complete response in a patient with metastatic breast cancer and BRCA1/2 mutations.
- Rucaparib was effective as maintenance therapy after initial treatment in another patient with BRCA1/2 mutations.

## Abstract

Triple-negative breast cancer poses distinct challenges because it lacks hormone receptors and does not have human epidermal growth factor receptor 2 (HER2) amplification. Mutations in BRCA1/2 genes are associated with homologous recombination deficiency tumors, rendering them susceptible to poly (ADP-ribose) polymerase (PARP) inhibitors. Notably, germline BRCA1/2 mutations are linked to distinct clinical features, including an increased risk of triple-negative breast cancer (TNBC) and a younger age of onset. PARP inhibitors such as olaparib and talazoparib have demonstrated efficacy in patients with BRCA mutations, leading to FDA approvals for ovarian and breast cancers. However, there remains limited data on PARP inhibitor response rates in patients with somatic BRCA mutations. This case series demonstrates the use of rucaparib in metastatic breast cancer patients harboring both germline and somatic BRCA1/2 mutations, discussing the advancing landscape of targeted therapies in breast cancer management. In the first case, despite undergoing anthracycline-based chemotherapy followed by hormonal therapy, disease progression ensued. However, transitioning to rucaparib yielded a remarkable complete response lasting over two years, highlighting its efficacy in this clinical setting. Similarly, in the second case, rucaparib demonstrated effectiveness as a maintenance therapy subsequent to achieving a near-complete response to taxane and platinum-based treatment. These findings emphasize the promising role of rucaparib in managing metastatic breast cancer in patients with BRCA1/2 mutations, further contributing to the expanding armamentarium of targeted therapies in breast cancer care.

## Linked entities

- **Genes:** BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672], BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675]
- **Diseases:** triple-negative breast cancer (MONDO:0005494)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672] {aka BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4}
- **Diseases:** TNBC (MESH:D064726), Metastatic (MESH:D000092182), Breast Cancer (MESH:D001943), homologous recombination deficiency tumors (MESH:C535296), ovarian and breast cancers (MESH:D061325)
- **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/PMC11193870/full.md

## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC11193870/full.md

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Source: https://tomesphere.com/paper/PMC11193870