# Efficacy and safety of intraoperative hyperthermic intraperitoneal chemotherapy for locally advanced colorectal cancer (HIPECT4): final analysis of randomized clinical trial

**Authors:** Alvaro Arjona-Sánchez, Alberto Gutiérrez-Calvo, Juan J Segura-Sampedro, Rafael Morales, Estibalitz Pérez-Viejo, Vanessa Concepción-Martín, Susana Sánchez-García, Alfonso García-Fadrique, Isabel Prieto-Nieto, Lana Bijelic, Juan Torres-Melero, Maria Ramirez-Faraco, Arancha Prada-Villaverde, Joaquin Carrasco-Campos, Manuel Artiles-Armas, Pedro Villarejo-Campos, Gloria Ortega-Pérez, Enrique Boldo-Roda, Juan M Sánchez-Hidalgo, Angela Casado-Adam, Lidia Rodríguez-Ortiz, Blanca Rufian-Andújar, Enrique Aranda, Maria T Cano-Osuna, Cesar Díaz-López, Antonio Romero-Ruiz, Maria Carmen Vazquez-Borrego, Sebastian Rufián-Peña

PMC · DOI: 10.1093/bjsopen/zrag002 · BJS Open · 2026-03-27

## TL;DR

A clinical trial found that using heated chemotherapy during surgery can reduce peritoneal recurrence in advanced colon cancer without causing more side effects.

## Contribution

The study provides long-term evidence that HIPEC with mitomycin C reduces peritoneal metastases in locally advanced colon cancer.

## Key findings

- HIPEC improved locoregional control with a hazard ratio of 0.19 compared to standard treatment.
- HIPEC reduced peritoneal recurrence without increasing toxicity.
- Subgroup analysis showed better locoregional control for pT4 colon cancer patients receiving HIPEC.

## Abstract

Despite adjuvant systemic chemotherapy after surgical resection in patients with pT4 stage colon cancer, a high percentage of them will develop peritoneal metastases. Intraoperative hyperthermic intraperitoneal chemotherapy (HIPEC) is a treatment option with the goal of preventing metachronous peritoneal metastases. The aim of this study was to report the longer-term outcomes of peritoneal control with the use of intraoperative HIPEC based on mitomycin C after the last enrolled patient of the HIPECT4 trial reached 36 months follow-up.

Between November 2015 and March 2021, patients with resectable primary clinical T4 N0-2M0 were included and randomized (1:1) to either adjuvant HIPEC with mitomycin C (30 mg/m2, 60 minutes) or standard treatment. The primary endpoint was locoregional control at 36 months. Kaplan–Meier survival analysis with a log-rank test was used to compare the two study groups.

A total of 184 patients were included and followed up at 36 months. The locoregional control rate was improved with HIPEC compared with adjuvant chemotherapy alone (hazard ratio 0.19, 95% confidence interval 0.04 to 0.86; P = 0.031). Three years overall survival and disease-free survival did not differ between patients assigned to the HIPEC and control groups. Subgroup analysis showed better locoregional control with the use of HIPEC for patients with definitive pT4 colon cancer (hazard ratio 0.08, 0.01 to 0.65; P = 0.017) and per protocol (receiving adjuvant chemotherapy) patients (hazard ratio 0.18, 0.04 to 0.83; P = 0.028). The pattern of recurrence was modified significantly using HIPEC with less peritoneal relapse.

The long-term outcome analysis of the HIPECT4 trial demonstrated that using mitomycin C-based HIPEC reduced peritoneal recurrence in patients with locally advanced colon cancer without increasing toxicity. However, there was no difference in overall survival and disease-free survival.

NCT02614534 (https://clinicaltrials.gov/).

Hyperthermic intraperitoneal chemotherapy in prophylaxis reduces locoregional relapse in locally advanced colon cancer, demonstrated in results from long-term follow-up.

## Linked entities

- **Chemicals:** mitomycin C (PubChem CID 5746)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, ZHX2 (zinc fingers and homeoboxes 2) [NCBI Gene 22882] {aka AFR1, RAF}
- **Diseases:** HIPEC (MESH:D000084202), toxicity (MESH:D064420), perforation (MESH:D057112), Morbidity (OMIM:614963), Colorectal cancer (MESH:D015179), peritoneal (MESH:D010538), metastases (MESH:D009362), peritoneal carcinomatosis (MESH:D010534), mucinous cancers (MESH:D009369)
- **Chemicals:** oxaliplatin (MESH:D000077150), FOLFOX (MESH:C410216), CAPOX (-), mitomycin C (MESH:D016685), panitumumab (MESH:D000077544), T3 (MESH:D014284)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** N0 — Homo sapiens (Human), Familial hypertrophic cardiomyopathy type 26, Induced pluripotent stem cell (CVCL_A6XE)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13023033/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023033/full.md

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Source: https://tomesphere.com/paper/PMC13023033