Evaluating MRI response criteria in microsatellite instability-high rectal cancer treated with immune checkpoint

Q Vanderbecq1, R Cohen2, M Camus3

  • 1Department of Radiology, AP-HP, Sorbonne, Saint-Antoine Hospital, Paris, France; UMR 7371, Université Sorbonne, CNRS, Inserm U114615, Paris, France.

ESMO Open
|December 30, 2025
PubMed
Abstract

Insights

Magnetic resonance imaging (MRI) shows unique patterns after anti-programmed cell death protein 1 (PD-1) therapy for rectal cancer. These findings differ from standard criteria, requiring updated imaging assessments for patients with microsatellite instability-high (MSI-H) or mismatch repair-deficient (dMMR) rectal cancer.

Area of Science:

  • Oncology
  • Radiology
  • Immunotherapy

Background:

  • Immune checkpoint inhibitors (ICIs), specifically anti-PD-1 agents, are used for microsatellite instability-high (MSI-H) or mismatch repair-deficient (dMMR) rectal cancer.
  • Standard MRI criteria for response assessment were developed for chemoradiotherapy and may not apply to ICI treatment.
  • Accurate response evaluation is crucial for non-operative management and surgical decisions.

Purpose of the Study:

  • To investigate MRI-based response patterns in patients with MSI-H/dMMR rectal cancer treated with neoadjuvant anti-PD-1 monotherapy.
  • To compare these patterns with those typically seen after conventional chemoradiotherapy.
  • To highlight the need for adapted MRI criteria in the context of ICI therapy.

Main Methods:

  • Retrospective analysis of 14 patients with locally advanced MSI-H/dMMR rectal adenocarcinoma.
  • Treatment involved neoadjuvant anti-PD-1 monotherapy.
  • MRI included T2-weighted, diffusion-weighted, and contrast-enhanced sequences.
  • Pathological complete response was confirmed via surgery or endoscopic/biopsy-confirmed complete remission.

Main Results:

  • All 14 patients achieved a pathological complete response.
  • Observed MRI patterns included split scar sign (2), fibrotic response (5), lesion disappearance (1), and residual intermediate T2 signal (6).
  • Mucinous tumors consistently showed T2-hyperintense residues, and fibrotic responses sometimes persisted beyond 3 months.
  • Histological analysis in surgical cases revealed residual mucin without viable tumor cells.

Conclusions:

  • MRI response patterns following anti-PD-1 monotherapy for MSI-H/dMMR rectal cancer are distinct from those after chemoradiotherapy.
  • Current imaging criteria may require adaptation for accurate response assessment in the ICI setting.
  • Persistent MRI abnormalities are common despite complete pathological response, necessitating careful interpretation for surgical decision-making.

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