# Complete pathological response with pembrolizumab in recurrent sigmoid adenocarcinoma

**Authors:** Benson Li, Truong Ma

PMC · DOI: 10.1093/jscr/rjag168 · Journal of Surgical Case Reports · 2026-03-21

## TL;DR

A patient with recurrent colorectal cancer achieved a complete pathological response after treatment with pembrolizumab, an immunotherapy drug.

## Contribution

This case demonstrates pembrolizumab's potential to induce complete response in dMMR colorectal cancer without radiographic regression.

## Key findings

- The patient showed no residual malignancy after 20 cycles of pembrolizumab.
- Complete pathological response was observed despite no visible radiographic regression.
- Pembrolizumab may be an effective treatment for dMMR colorectal cancer recurrence.

## Abstract

Genetic evaluation for mismatch repair deficiency (dMMR) or microsatellite instability (MSI) is now routinely performed as part of the workup of colorectal cancer. The traditional approach to advanced disease was chemotherapy-based agents; however, dMMR/MSI patients were found to respond more poorly. Immunotherapy, such as pembrolizumab, a programmed cell death protein-1 inhibitor, has evolved as a superior option. This report describes a 48-year-old with a history of stage IIC sigmoid adenocarcinoma who developed recurrent uterine and peritoneal implants following surgical resection and adjuvant chemotherapy. Given the concern for recurrent disease, the appropriateness of colostomy reversal remained uncertain. The patient subsequently underwent 20 cycles of pembrolizumab followed by colostomy reversal with concurrent resection of suspected implants. Final pathology revealed a complete pathological response (cPR) with no evidence of residual malignancy. This case highlights the potential for pembrolizumab to induce a cPR in dMMR colorectal cancer despite the absence of radiographic regression.

## Linked entities

- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** colorectal cancer (MESH:D015179), sigmoid adenocarcinoma (MESH:D000230), MSI (MESH:D053842), malignancy (MESH:D009369), mismatch repair deficiency (MESH:C536928)
- **Chemicals:** pembrolizumab (MESH:C582435)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC13005662/full.md

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Source: https://tomesphere.com/paper/PMC13005662