# Primary fallopian tube cancer followed by primary breast cancer in RAD51C mutation carrier treated with niraparib as first line maintenance therapy: a case report

**Authors:** Hua Yuan, Rong Zhang, Ning Li, Hongwen Yao

PMC · DOI: 10.1186/s13053-024-00274-8 · 2024-02-15

## TL;DR

A woman with a rare RAD51C mutation developed breast cancer after being treated for fallopian tube cancer with niraparib, highlighting potential risks in mutation carriers.

## Contribution

This is the first reported case of metachronous breast cancer in a RAD51C mutation carrier with fallopian tube cancer during PARPi treatment.

## Key findings

- The patient developed invasive ductal breast cancer after 36 months of niraparib treatment.
- The breast cancer was stage IIA with axillary lymph node involvement.
- No distant metastases were found at the time of breast cancer diagnosis.

## Abstract

Given the rarity of RAD51C mutations, the risk and treatment of metachronous breast cancer after the diagnosis of ovarian cancer in RAD51C mutation carriers is not clear, especially for those who have received PARPi treatment. We report the case of a 65-year-old woman diagnosed with stage IIIC high-grade serous primary fallopian tube cancer. The patient had no family history of breast or ovarian cancer. The patient received three cycles of neoadjuvant chemotherapy with paclitaxel and carboplatin and achieved a complete response. After interval debulking surgery, the patient received three cycles of adjuvant chemotherapy. Collection and extraction of saliva DNA for next-generation sequencing identified a RAD51C mutation c.838-2 A > G. The patient received niraparib as front-line maintenance treatment. After 36 months of niraparib treatment, the patient had grade II invasive ductal carcinoma of the left breast that was positive for estrogen receptor (90%) and Ki-67 (30%) and negative for progesterone receptor and human epidermal growth factor receptor 2. Computed tomography revealed the absence of distant metastases. Modified radical mastectomy and axillary lymph node dissection were then performed. The final pathological report of the breast showed a 1.8 cm Bloom-Richardson grade II invasive ductal carcinoma in the left breast with axillary lymph node metastasis (1/21). Finally, the breast cancer was stage IIA, pT1cN1M0. The metachronous breast cancer in this case may be the first report of second primary cancer in fallopian tube cancer patient harboring a RAD51C mutation during niraparib treatment. Further studies are required to determine optimal treatment.

## Linked entities

- **Genes:** RAD51C (RAD51 paralog C) [NCBI Gene 5889]
- **Chemicals:** niraparib (PubChem CID 24958200), paclitaxel (PubChem CID 36314), carboplatin (PubChem CID 426756)
- **Diseases:** fallopian tube cancer (MONDO:0002158), breast cancer (MONDO:0004989)

## 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}, RAD51C (RAD51 paralog C) [NCBI Gene 5889] {aka BROVCA3, FANCO, R51H3, RAD51L2}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}
- **Diseases:** metastases (MESH:D009362), ovarian cancer (MESH:D010051), invasive ductal carcinoma of the left breast (MESH:D018270), breast cancer (MESH:D001943), primary cancer (MESH:D009369), stage IIIC (MESH:C566891), invasive ductal carcinoma (MESH:D044584), breast or ovarian cancer (MESH:D061325), axillary lymph node metastasis (MESH:D008207), Primary fallopian tube cancer (MESH:D005185)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** c.838-2 A > G

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10868093/full.md

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Source: https://tomesphere.com/paper/PMC10868093