# Treatment of Ovarian Clear Cell Carcinoma: A Case of Successful Management With Targeted Therapies

**Authors:** Sydney Pence, Kellie Rath, Aine Clements

PMC · DOI: 10.1155/crog/1319978 · 2025-07-12

## TL;DR

A patient with advanced ovarian clear cell carcinoma responded well to targeted therapies after standard treatments failed.

## Contribution

Demonstrates successful use of alpelisib and immunotherapy in treating resistant ovarian clear cell carcinoma.

## Key findings

- Alpelisib provided a durable response based on genomic testing.
- Nivolumab and ipilimumab combination showed partial response after alpelisib progression.
- Targeted therapies offer promising options for advanced ovarian clear cell carcinoma.

## Abstract

Background: Advanced stages of ovarian clear cell carcinoma have poorer prognoses than many other ovarian cancers. When standard treatments are ineffective, alternative options are needed.

Case: A 56-year-old woman was diagnosed with ovarian clear cell carcinoma and treated with surgical management as well as carboplatin and paclitaxel. At recurrence, her disease progressed despite multiple chemotherapy regimens. A durable response was achieved first with alpelisib, chosen based on genomic testing. When progression occurred on this agent, a partial disease response was achieved with the combination of nivolumab and ipilimumab.

Conclusion: The use of targeted therapies as well as the combination of nivolumab and ipilimumab is a promising option in advanced and recurrent cases of ovarian clear cell carcinoma.

## Linked entities

- **Chemicals:** carboplatin (PubChem CID 426756), paclitaxel (PubChem CID 36314), alpelisib (PubChem CID 56649450)

## Full-text entities

- **Diseases:** Ovarian Clear Cell Carcinoma (MESH:D010051)
- **Chemicals:** alpelisib (MESH:C585539), nivolumab (MESH:D000077594), carboplatin (MESH:D016190), paclitaxel (MESH:D017239), ipilimumab (MESH:D000074324)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12276056/full.md

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Source: https://tomesphere.com/paper/PMC12276056