# A Meta-Analysis on the Long-Term Impact of Cytoreductive Surgery Plus HIPEC for Ovarian Cancer with Peritoneal Metastasis: Are We on the Right Path?

**Authors:** Dan Brebu, Mircea Șelaru, Ionut Flaviu Faur, Mihai Cosmin Burta, Ioana Adelina Faur, Amadeus Dobrescu, Ciprian Duță, Vlad Braicu, Andreea-Adriana Neamțu, Danau Răzvan

PMC · DOI: 10.3390/life16020335 · Life · 2026-02-14

## TL;DR

This study reviews the effectiveness of combining surgery with heated chemotherapy for ovarian cancer spread to the abdomen, finding potential survival benefits but limited evidence.

## Contribution

The paper provides a meta-analysis of survival and complication rates for CRS plus HIPEC in ovarian cancer with peritoneal metastasis.

## Key findings

- CRS plus HIPEC was associated with improved overall and progression-free survival in limited evidence.
- The pooled severe complication rate was 18%, and the high CC-0 rate suggests effective cytoreduction.
- Current data suggest HIPEC should be used selectively in carefully chosen patients.

## Abstract

Background: The benefit of adding hyperthermic intraperitoneal chemotherapy (HIPEC) to cytoreductive surgery (CRS) in ovarian cancer with peritoneal metastasis remains debated outside selected indications. We performed a systematic review and meta-analysis to quantify survival, perioperative morbidity, and completeness of cytoreduction using study-level data. Methods: PubMed/MEDLINE, Embase, and Web of Science were searched. Eligible English-language studies included ovarian cancer patients undergoing CRS plus HIPEC and reported at least one of the following: overall survival (OS), progression-free survival (PFS), Grade III–IV complications, or CC-0 rate. Random-effects meta-analyses were conducted using inverse-variance pooling. For HR outcomes, DerSimonian–Laird τ2 with Hartung–Knapp confidence intervals was applied. Proportions were pooled using logit transformation (PLOGIT) with random-effects models. Results: Twelve studies (n = 567) were included. Only two studies provided extractable HRs for OS and PFS (n = 217). CRS plus HIPEC was associated with improved OS (HR 0.68, 95% CI 0.52–0.90, p = 0.0023; I2 = 0%; prediction interval 0.14–3.34) and improved PFS (HR 0.70, 95% CI 0.31–1.57, p = 0.0007; I2 = 0%; prediction interval 0.18–2.66). Across 12 studies (n = 563), the pooled Grade III–IV complication rate was 0.18 (95% CI 0.14–0.22; I2 = 16.3%; prediction interval 0.12–0.26). In 10 studies (n = 385), the pooled CC-0 rate was 0.87 (95% CI 0.79–0.92; I2 = 46.7%; prediction interval 0.66–0.96). Conclusions: CRS plus HIPEC shows a favorable signal for OS and PFS in the limited HR-eligible evidence and appears feasible, with a pooled severe complication rate of ~18% and high CC-0 rates. Current data support HIPEC primarily as a targeted intensification strategy in carefully selected patients, while broader adoption requires additional randomized, context-specific evidence.

## Linked entities

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

## Full-text entities

- **Genes:** BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672] {aka BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4}
- **Diseases:** metabolic (MESH:D008659), HIPEC (MESH:D000084202), Epithelial ovarian cancer (MESH:D000077216), Peritoneal Cancer (MESH:D010534), tumor (MESH:D009369), complication (MESH:D008107), intraperitoneal disease (MESH:D004194), injury to (MESH:D014947), peritoneal disease (MESH:D010532), postoperative (MESH:D019106), Ovarian Cancer (MESH:D010051), gynecologic malignancy (MESH:D005833), Postoperative Complications (MESH:D011183), Peritoneal Metastasis (MESH:D010538), stage III disease (MESH:D007676), cytotoxicity (MESH:D064420), deaths (MESH:D003643), CRS (MESH:D000267), OS (MESH:D011475)
- **Chemicals:** platinum (MESH:D010984), Cisplatin (MESH:D002945)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** OVHIPEC-1 — Mus musculus (Mouse), Hybridoma (CVCL_C7RB), OVHIPEC-2 — Homo sapiens (Human), Colon carcinoma, Cancer cell line (CVCL_A628)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942593/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942593/full.md

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Source: https://tomesphere.com/paper/PMC12942593