For cancers that have spread across the lining of the abdomen, HIPEC offers something other treatments cannot — a real chance of long-term control, and for some, cure. Dr. Vinod T. Gore performs cytoreductive surgery (CRS) to remove all visible tumour, then bathes the abdomen in heated chemotherapy to destroy microscopic disease left behind, in a single combined operation.
Some abdominal cancers spread not through the bloodstream but across the peritoneum — the thin membrane lining the abdominal cavity. This is called peritoneal carcinomatosis or peritoneal surface malignancy. Ordinary intravenous chemotherapy struggles to reach these deposits, because the peritoneum has a poor blood supply.
HIPEC tackles the problem in two stages, in one operation. First, cytoreductive surgery (CRS) — the surgeon meticulously removes every visible tumour deposit from the peritoneal surfaces and affected organs. This can take many hours.
Then comes HIPEC — Hyperthermic Intraperitoneal Chemotherapy. Heated chemotherapy (around 41–43 °C) is circulated throughout the abdominal cavity for 30–90 minutes, reaching every surface directly. The heat itself damages cancer cells and makes the chemotherapy far more effective, while keeping most of the drug inside the abdomen rather than the bloodstream.
The combination targets what each alone cannot: surgery clears visible disease, and heated chemotherapy destroys the microscopic cells left behind. Success depends on achieving a complete cytoreduction.
HIPEC is not for every abdominal cancer. It is most effective when disease is confined to the peritoneal surfaces and can be completely removed. The strength of evidence differs by tumour type, so each indication is weighed individually at the tumour board.
| Cancer / Disease | Role of CRS + HIPEC | Evidence | Key trial | Typical HIPEC drug |
|---|---|---|---|---|
| Pseudomyxoma Peritonei | Standard of care; potentially curative with complete cytoreduction | Strong | Large international registries | Mitomycin-C |
| Appendiceal cancer (mucinous & non-mucinous) |
Well-established; resection of peritoneal disease + HIPEC | Strong | Registry & cohort data | Mitomycin-C |
| Peritoneal mesothelioma | Standard of care at specialist centres; markedly improves survival | Strong | Multi-institutional series | Cisplatin ± Doxorubicin |
| Colorectal peritoneal metastases | Complete cytoreduction is the key benefit; HIPEC used selectively | Selective | PRODIGE-7 (2021) | Oxaliplatin / Mitomycin-C |
| Ovarian cancer (interval, selected) | Survival benefit when added to interval debulking after chemotherapy | Supported | van Driel, NEJM 2018 | Cisplatin |
| Gastric cancer (selected) | Limited peritoneal disease / selected cases; evidence still evolving | Investigational | GASTRIPEC; ongoing trials | Mitomycin-C / Cisplatin |
Drugs and timing are individualised per tumour type, prior chemotherapy and renal function, and decided at the multidisciplinary tumour board. Perfusion is typically delivered at 41–43 °C for 30–90 minutes.
This is one of the longest and most complex operations in surgical oncology — often 8 to 12 hours. It is delivered by an experienced team with specialist anaesthesia and critical-care support.
| Region (0–12) | Area assessed | Lesion Size score | Meaning |
|---|---|---|---|
| 0–8 | Central, right/left upper & lower, flanks, epigastrium, pelvis | LS 0 | No tumour visible |
| 9–12 | Upper & lower jejunum, upper & lower ileum | LS 1 | Nodules up to 0.5 cm |
| Each of the 13 regions is scored LS 0–3 → | LS 2 | Nodules 0.5–5 cm | |
| Total PCI = sum of all regions (0–39) | LS 3 | Nodules > 5 cm or confluent | |
Reading the total (Sugarbaker): lower PCI predicts a higher chance of complete cytoreduction and better outcomes. As a general guide, colorectal peritoneal disease is most favourable at PCI < 20 (and especially < 12); pseudomyxoma can be resected at much higher indices. PCI is an aid to judgement, weighed with disease type, location and fitness — not a rigid cut-off.
| Score | Residual disease after surgery | Prognostic meaning |
|---|---|---|
| CC-0 | No visible residual tumour | Optimal — the goal |
| CC-1 | Residual nodules ≤ 2.5 mm | Complete — HIPEC can penetrate |
| CC-2 | Residual nodules 2.5 mm – 2.5 cm | Incomplete |
| CC-3 | Residual nodules > 2.5 cm | Incomplete |
Why CC matters most: heated chemotherapy penetrates only 2–3 mm, so it can only sterilise microscopic disease. The survival benefit of the whole operation depends on achieving CC-0 or CC-1. If complete cytoreduction cannot be achieved, HIPEC offers little — which is why honest patient selection comes first.
The disease table above summarises the evidence and key trial for each indication. Two findings deserve a closer word, because they shape how HIPEC should — and should not — be used.
CRS + HIPEC is major surgery with a real recovery. Being prepared for it — and being cared for by a team that does this regularly — makes the difference.
This page is general information, not personal medical advice. Suitability for CRS + HIPEC is always decided individually at a multidisciplinary tumour board. Please bring all scans, histopathology and previous operative notes to your consultation.
If you or a family member has peritoneal spread from an abdominal cancer, an early specialist opinion matters — suitability for HIPEC depends on acting before disease becomes too extensive. Please bring all CT/MRI/PET scans, biopsy and histopathology reports, and any previous operative notes — ideally on CD or shared via WhatsApp in advance.