# The added value of chemotherapy after secondary cytoreductive surgery in unifocal versus multifocal first recurrent epithelial ovarian cancer: A systematic review

**Authors:** R.E.W.M. van de Vorst, M.D. Huiskamp, E.H. Gort, P.O. Witteveen, R.P. Zweemer, C.G. Gerestein

PMC · DOI: 10.1016/j.gore.2025.101809 · Gynecologic Oncology Reports · 2025-07-18

## TL;DR

This review finds that unifocal first recurrent ovarian cancer patients have better survival after surgery and chemotherapy than those with multifocal recurrence, but more research is needed.

## Contribution

The study highlights a lack of research on chemotherapy's added value after surgery in unifocal versus multifocal first recurrent ovarian cancer.

## Key findings

- Unifocal first recurrent EOC shows better progression-free and overall survival after secondary surgery and chemotherapy.
- Few studies exist on chemotherapy's added value after secondary cytoreductive surgery in this context.
- Survival benefits varied across studies, with some showing no significant difference after adjusting for other factors.

## Abstract

•No studies assess chemotherapy after secondary debulking in unifocal versus multifocal first recurrent ovarian cancer.•Unifocal first recurrent EOC shows better PFS and OS than multifocal recurrence after secondary debulking with chemotherapy.•Future RCTs should evaluate the added value of chemotherapy after secondary debulking in unifocal first recurrent EOC.

No studies assess chemotherapy after secondary debulking in unifocal versus multifocal first recurrent ovarian cancer.

Unifocal first recurrent EOC shows better PFS and OS than multifocal recurrence after secondary debulking with chemotherapy.

Future RCTs should evaluate the added value of chemotherapy after secondary debulking in unifocal first recurrent EOC.

This systematic review aims to evaluate the added value of chemotherapy after secondary cytoreductive surgery (SCS) on survival in patients with unifocal and multifocal first recurrent epithelial ovarian cancer (EOC). Moreover, it compares survival outcomes between unifocal and multifocal recurrences in treatment outcomes.

A systematic search was conducted across PubMed, Embase, and the Cochrane Library identified 907 articles. Studies were selected if they involved patients with first recurrent EOC undergoing SCS, stratified by unifocal or multifocal recurrence. The primary outcomes were progression-free survival (PFS) and overall survival (OS).

No studies specifically addressed the added value of chemotherapy after SCS in unifocal versus multifocal first recurrent EOC. This systematic review identified eight studies examining PFS and OS in patients with unifocal and multifocal first recurrent EOC following SCS with chemotherapy. Findings consistently show that unifocal first recurrent EOC is associated with significantly improved PFS and OS compared to multifocal first recurrent EOC. However, the extent of the survival benefit varied. Six studies showed an advantage for unifocal recurrence on multivariate analyses, although two studies did not find statistically significant differences after adjusting for other variables.

This review shows that there is a knowledge gap regarding the added value of chemotherapy after complete SCS in first recurrent EOC. However, this review shows a survival advantage of unifocal over multifocal first recurrent EOC. There is a need for clinical trials to compare survival outcomes between unifocal and multifocal first recurrent EOC patients undergoing SCS alone or SCS with chemotherapy.

## Linked entities

- **Diseases:** ovarian cancer (MONDO:0005140), epithelial ovarian cancer (MONDO:0005140)

## Full-text entities

- **Genes:** MUC16 (mucin 16, cell surface associated) [NCBI Gene 94025] {aka CA125}
- **Diseases:** toxicities (MESH:D064420), SCS (MESH:D000068376), EOC (MESH:D000077216), nausea (MESH:D009325), ovarian cancer (MESH:D010051), tumor (MESH:D009369), dead (MESH:D001926), ototoxicity (MESH:D006311), peritoneal carcinomatosis (MESH:D010534), ascites (MESH:D001201), neurotoxicity (MESH:D020258), carcinomatosis (MESH:D002277), intra-abdominal lesion (MESH:D000082122), death (MESH:D003643)
- **Chemicals:** Platinum (MESH:D010984), SCS (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12320076/full.md

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Source: https://tomesphere.com/paper/PMC12320076