# Modification of RECIST 1.1 criteria for assessing response in breast tumours treated with radiation therapy using multiparametric breast MRI: Radiology and oncology perspective

**Authors:** E. Durie, M. Morris, N.A. Healy, S. Salehi-Bird, A. Seth, P. Haria, N. Tunariu, S. Allen, Aditi Chandra, Shalini Sahu, Rakesh Anandarajan, Miklos Barta, Ioannis Roxanis, F.H. Cafferty, M.D. Blackledge, N. Somaiah

PMC · DOI: 10.1016/j.breast.2026.104750 · 2026-03-12

## TL;DR

This paper proposes modified criteria for assessing breast tumor response to radiation therapy using multiparametric MRI to better distinguish fibrosis from residual disease.

## Contribution

The paper introduces new MRI-based response criteria to address limitations of RECIST 1.1 in evaluating breast tumors treated with radiation.

## Key findings

- RECIST 1.1 has limitations in assessing breast tumors treated with radiation due to fibrosis.
- Multiparametric MRI can differentiate fibrosis and residual disease more effectively.
- Modified criteria using T2W, CE T1W, and DWI sequences are proposed for response evaluation.

## Abstract

The traditional, size-based, RECIST 1.1 guideline is the standard for assessing tumour response, but has notable limitations, particularly for breast tumours treated with radiotherapy (RT). RT often induces fibrosis, leading to a persisting measurable abnormality on T1W/T2W MRI sequences despite an underlying pathological response. As pre-operative RT trials expand and omission of surgery is being tested, having anatomico-functional MRI response criteria may facilitate more accurate response evaluation. We propose modified RECIST 1.1 criteria based on 3 sequences of multiparametric MRI (mpMRI): unenhanced T2W, contrast-enhanced (CE) T1W and diffusion-weighted imaging (DWI). Key recommendations include complete response defined as 1) resolution of tumour mass on all sequences, or 2) evidence of residual T2 abnormality with CE images showing no enhancement above background parenchymal enhancement (BPE) and DWI signal consistent with necrosis/fibrosis, or 3) minimal evidence of enhancement above BPE with DWI in keeping with fibrosis. Criteria are also defined for other response categories (partial response/stable disease/progression). These recommendations can be tested in future trials and offer guidance on the interpretation of mpMRI sequences when breast tumours are treated in situ with radiation, a scenario in which little published data currently exists. They highlight how DWI can aid RT response assessment and help overcome some limitations with current RECIST criteria.

•Size-based RECIST 1.1 criteria have notable limitations.•Breast tumours develop fibrosis when treated with primary RT.•Multiparametric MRI images can help distinguish fibrosis and residual disease.•Modified criteria for RT response assessment with multiparametric MRI are presented.

Size-based RECIST 1.1 criteria have notable limitations.

Breast tumours develop fibrosis when treated with primary RT.

Multiparametric MRI images can help distinguish fibrosis and residual disease.

Modified criteria for RT response assessment with multiparametric MRI are presented.

## Linked entities

- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Diseases:** SD (MESH:D060050), rectal cancers (MESH:D012004), scarring (MESH:D002921), necrosis (MESH:D009336), BCs (MESH:D001943), T2 abnormality (MESH:C535434), skin (MESH:D012871), head and neck and pancreatic cancers (MESH:D006258), oedema (MESH:C536897), CR (MESH:D001766), PD (MESH:D018450), Fat (MESH:D004620), PR (MESH:D004828), Tumour (MESH:D009369), Fibrosis (MESH:D005355)
- **Chemicals:** water (MESH:D014867), BioRender (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13014914/full.md

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Source: https://tomesphere.com/paper/PMC13014914