Clinical calculator summary
Peritoneal Cancer Index (PCI)
Clinical calculator summary
Peritoneal Cancer Index (PCI)
A 0-39 score that sums the largest visible implant category across 13 peritoneal regions.
Evidence-based context for fast calculator use
- Purpose:
- Standardize documentation of macroscopic peritoneal disease burden.
- Population:
- Patients with peritoneal metastases or a peritoneal surface malignancy undergoing radiologic, laparoscopic, or operative assessment.
- Factors:
- Complete 13-region assessment, Largest implant per region, Confluent disease, Assessment modality, Primary tumor context
- Reference:
- Jacquet and Sugarbaker, Cancer Treat Res. 1996;82:359-374.
Peritoneal Carcinomatosis Index (PCI)
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
Required regional assessment. LS-0 means the region was examined and no visible tumor was found.
PCI region map
Score 13 regions before CRS-HIPEC discussion
Right upper
Epigastrium
Left upper
Right flank
Central
Left flank
Right lower
Pelvis
Left lower
Regions 0-8 cover the abdominopelvic grid. Regions 9-12 capture small-bowel involvement, which can strongly affect complete cytoreduction feasibility.
Small bowel regions
Lesion-size score
Use before referral
Summarize tumor distribution for a peritoneal surface malignancy or tumor board review.
Flag small bowel
A modest total PCI can still be challenging when bowel or mesentery disease is extensive.
Pair with CC score
PCI describes burden before cytoreduction; CC score documents residual disease after surgery.
Clinical Context & Background
PCI = sum of LS-0 to LS-3 scores for regions 0 through 12. Valid total: 0 to 39.Reference Data
| Lesion-size score | Required regional assessment |
|---|---|
| LS-0 | No visible tumor in an explicitly assessed region |
| LS-1 | Largest implant ≤5 mm |
| LS-2 | Largest implant >5 mm and ≤50 mm |
| LS-3 | Largest implant >50 mm or confluent disease |
| Total PCI | Sum all 13 regional scores; range 0-39 |
Clinical Workflow
Use, Interpret, And Continue The Patient Pathway
Expand for workflow guidance, limitations, examples, and related next steps.
Clinical Workflow
Use, Interpret, And Continue The Patient Pathway
Expand for workflow guidance, limitations, examples, and related next steps.
When To Use
- Use to document peritoneal disease distribution during structured imaging, laparoscopy, laparotomy, referral, or multidisciplinary review.
- Record all 13 regions explicitly and identify whether the score is radiologic, laparoscopic, or operative.
- Use the largest visible implant in each region; confluent disease is LS-3 regardless of individual nodule size.
How To Interpret
- The total PCI ranges from 0 to 39 and describes macroscopic disease burden and distribution.
- The original PCI does not define universal low, moderate, or high categories.
- Interpretation and treatment thresholds are disease-specific and must account for distribution, biology, resectability, and assessment modality.
What To Do Next
- Document the assessment modality and separately describe small-bowel/mesenteric involvement, extra-peritoneal disease, performance status, and anticipated resectability.
- Use the PCI versus CC score guide when distinguishing pre-cytoreduction disease burden from post-cytoreduction residual disease.
- Discuss treatment implications in a peritoneal surface malignancy multidisciplinary team rather than applying a universal PCI cutoff.
Limitations
- Do not use an unassessed region as LS-0.
- Do not treat radiologic, laparoscopic, and operative PCI as interchangeable.
- Do not use PCI alone to determine CRS, HIPEC, prognosis, or treatment eligibility.
Validated Population
Originally developed for peritoneal carcinomatosis staging and now used across peritoneal surface malignancies; disease-specific interpretation is required.
Clinical Example
A PCI of 12 documents the sum and distribution of regional disease. It does not by itself define low or moderate burden or determine CRS-HIPEC eligibility.
Calculation verification history
Verified
Calculation verification history
Verified: Production browser revalidation
- Three source-backed cases passed through all thirteen visible region controls at PCI totals 0, 18, and 39.
- Total and small-bowel subscores matched the Sugarbaker lesion-size sum exactly without unsupported universal risk bands or treatment cutoffs.
- No unexpected N/A, stale control, literal undefined/null value, or browser-console error was observed.
Case-level evidence is retained in validation/browser-revalidation/peritoneal-carcinomatosis-index-pci-2026-08-03.json.
: Production browser validation
- Ten source-backed cases were exercised on the public production route through visible browser controls; 10/10 case records passed their expected-versus-observed assertions across 12 visible submissions.
- Overall browser status: failed-console. medium: Production emitted minified React error #418 during route loads/reloads used by this run.
- Case-level inputs, expected and observed results, reset/repeat behavior, failure reproductions, and console evidence are retained in the production-browser evidence record.
Case-level production evidence is retained in validation/browser-production/peritoneal-carcinomatosis-index-pci.json.
: Full validation test
- Checked all 13 regions, LS-0 to LS-3 boundaries, representative totals from 0 to 39, and incomplete or invalid assessments.
: Correction
- Required an explicit valid selection for every region instead of silently treating unassessed regions as LS-0.
- Corrected LS-1 to include exactly 5 mm and LS-2 to include exactly 50 mm.
- Removed unsupported universal tumor-burden categories and the uncited small-bowel warning threshold.
Included in the current validation report.
Verification confirms the calculator implementation against the cited model; it is not independent clinical validation, regulatory approval, or medical advice.
Related Tools
Frequently Asked Questions
What does the PCI score measure?
PCI records macroscopic peritoneal disease burden by scoring the largest visible implant in each of 13 regions.
What if a region cannot be assessed?
Do not enter LS-0. LS-0 means the region was examined and no visible tumor was found. An incomplete assessment should be documented as incomplete rather than assigned a total PCI.
Is there one universal PCI cutoff for CRS-HIPEC?
No. The original score has no universal low, moderate, or high categories, and treatment thresholds vary by disease and clinical context.
How is PCI different from the CC score?
PCI describes disease burden before or during exploration. Completeness of Cytoreduction score describes visible residual disease after cytoreductive surgery.
What is the PCI score range?
The total ranges from 0 to 39. Each of 13 explicitly assessed regions receives an LS-0 to LS-3 score based on the largest visible implant or confluent disease.
Are radiologic, laparoscopic, and operative PCI interchangeable?
No. Record the assessment modality because visibility and access differ, and interpret the resulting PCI within that modality and disease context.
Evidence-based oncology decision support. Verify with clinical guidelines.