# Advances and challenges in the application of prophylactic hyperthermic intraperitoneal chemotherapy for gastric cancer

**Authors:** Muyang Liu, Xiaojun Shen

PMC · DOI: 10.3389/fonc.2026.1679522 · Frontiers in Oncology · 2026-02-10

## TL;DR

This paper reviews the use of prophylactic hyperthermic intraperitoneal chemotherapy (P-HIPEC) for gastric cancer to prevent peritoneal metastasis and improve patient outcomes.

## Contribution

The paper systematically reviews recent advances and challenges in P-HIPEC application for gastric cancer.

## Key findings

- P-HIPEC aims to reduce peritoneal metastasis after surgery by targeting residual cancer cells.
- Clinical efficacy and standardization of P-HIPEC remain areas of active research and debate.
- The review highlights the need for better patient and drug selection criteria for P-HIPEC.

## Abstract

Gastric cancer is the fifth most common malignant tumor worldwide and the third leading cause of cancer-related deaths, posing a serious threat to global public health. Despite notable advancements in surgical techniques, systemic chemotherapy, targeted therapy, and immunotherapy in recent years, the overall prognosis for patients with locally advanced gastric cancer (AGC) remains suboptimal, primarily due to the high propensity for local and distant metastasis. Peritoneal metastasis (PM), in particular, has become one of the most formidable clinical challenges owing to its high incidence, inherent resistance to systemic chemotherapy, and extremely poor prognosis. To address this challenge, Prophylactic Hyperthermic Intraperitoneal Chemotherapy (P-HIPEC) has emerged as a focal point of research. This therapeutic modality aims to eradicate microscopic residual tumors and free cancer cells in the abdominal cavity following radical gastrectomy, thereby effectively reducing the risk of peritoneal metastasis and improving long-term patient survival. This review systematically examines the latest research progress of P-HIPEC in the treatment of gastric cancer, provides an in-depth analysis of its mechanism of action, indications, criteria for patient and drug selection, evidence of clinical efficacy, safety controversies, and challenges in standardization. It also looks forward to future research directions in this field, with the aim of providing a valuable reference for clinical practice and academic research.

## Linked entities

- **Diseases:** gastric cancer (MONDO:0001056)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, PCDHB9 (protocadherin beta 9) [NCBI Gene 56127] {aka PCDH-BETA9, PCDH3H}, CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960] {aka CDW44, CSPG8, ECM-III, ECMR-III, H-CAM, HCELL}, PARP1 (poly(ADP-ribose) polymerase 1) [NCBI Gene 142] {aka ADPRT, ADPRT 1, ADPRT1, ARTD1, PARP, PARP-1}, CXCL12 (C-X-C motif chemokine ligand 12) [NCBI Gene 6387] {aka IRH, PBSF, SCYB12, SDF1, TLSF, TPAR1}, CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675] {aka BRCC2, BROVCA2, FACD, FAD, FAD1, FANCD}, SNAI1 (snail family transcriptional repressor 1) [NCBI Gene 6615] {aka SLUGH2, SNA, SNAH, SNAIL, SNAIL1, dJ710H13.1}, CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, TWIST1 (twist family bHLH transcription factor 1) [NCBI Gene 7291] {aka ACS3, BPES2, BPES3, CRS, CRS1, CSO}
- **Diseases:** HT (MESH:D005334), linitis plastica (MESH:D008039), dysfunction of vital organs (MESH:D009102), AGC (MESH:D013274), FCCs (MESH:D018295), pleural effusion (MESH:D010996), pneumonia (MESH:D011014), acute kidney injury (MESH:D058186), HIPEC (MESH:D000084202), fatigue (MESH:D005221), T4 tumors (MESH:D009369), pulmonary complications (MESH:D008171), Peritoneal Carcinomatosis (MESH:D010534), peritoneal failure (MESH:D051437), irritability (MESH:D001523), GS (MESH:D005736), trauma (MESH:D014947), disease (MESH:D004194), pain (MESH:D010146), necrosis (MESH:D009336), H (MESH:D000848), signet ring cell carcinoma (MESH:D018279), Renal impairment (MESH:D007674), lymph node metastasis (MESH:D008207), Intestinal obstruction (MESH:D007415), PM (MESH:D010538), bone marrow suppression (MESH:D001855), thrombocytopenia (MESH:D013921), Gastrointestinal complications (MESH:D005767), infection (MESH:D007239), cytotoxic (MESH:D064420), Anastomotic leak (MESH:D057868), metastases (MESH:D009362), anemia (MESH:D000740), OS (MESH:D011475), adhesions (MESH:D000267), Neutropenia (MESH:D009503), Hematological toxicity (MESH:D006402)
- **Chemicals:** Oxaliplatin (MESH:D000077150), 5-FU (MESH:D005472), PTX (MESH:D017239), Platinum (MESH:D010984), P (MESH:D010758), DOC (MESH:D000077143), CO2 (MESH:D002245), Taxanes (MESH:D043823), CDDP (-), Cisplatin (MESH:D002945), MMC (MESH:D016685)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12930464/full.md

## References

67 references — full list in the complete paper: https://tomesphere.com/paper/PMC12930464/full.md

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Source: https://tomesphere.com/paper/PMC12930464