MRI Apparent Diffusion Coefficient (ADC) as a Biomarker of Tumour Response: Imaging-Pathology Correlation in Patients with Hepatic Metastases from Colorectal Cancer (EORTC 1423)

Author:

Jackson Alan1,Pathak Ryan1,deSouza Nandita M.2ORCID,Liu Yan3ORCID,Jacobs Bart K. M.3,Litiere Saskia3,Urbanowicz-Nijaki Maria3,Julie Catherine45,Chiti Arturo67,Theysohn Jens8ORCID,Ayuso Juan R.9ORCID,Stroobants Sigrid10,Waterton John C.1ORCID

Affiliation:

1. Centre for Imaging Sciences, University of Manchester, Manchester M20 4GJ, UK

2. CRUK Cancer Imaging Centre, The Institute of Cancer Research and Royal Marsden NHS Foundation Trust, Downs Road, London SW7 3RP, UK

3. European Organisation for Research and Treatment of Cancer, 1200 Brussels, Belgium

4. EA 4340 BECCOH, UVSQ, Universite Paris-Saclay, 92104 Boulogne-Billancourt, France

5. Department of Pathology, APHP-Hopital Ambroise Pare, 92100 Boulogne-Billancourt, France

6. Nuclear Medicine Unit, IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy

7. Department of Bio-Medical Sciences, Humanitas University, 20072 Milan, Italy

8. Institute of Diagnostic and Interventional Radiology and Neuroradiology, University Hospital Essen, University Duisburg-Essen, 45122 Essen, Germany

9. Radiology Department—CDI, Hospital Clinic Universitari de Barcelona, 08036 Barcelona, Spain

10. Molecular Imaging and Radiology, University of Antwerp, 2000 Antwerp, Belgium

Abstract

Background: Tumour apparent diffusion coefficient (ADC) from diffusion-weighted magnetic resonance imaging (MRI) is a putative pharmacodynamic/response biomarker but the relationship between drug-induced effects on the ADC and on the underlying pathology has not been adequately defined. Hypothesis: Changes in ADC during early chemotherapy reflect underlying histological markers of tumour response as measured by tumour regression grade (TRG). Methods: Twenty-six patients were enrolled in the study. Baseline, 14 days, and pre-surgery MRI were performed per study protocol. Surgical resection was performed in 23 of the enrolled patients; imaging-pathological correlation was obtained from 39 lesions from 21 patients. Results: There was no evidence of correlation between TRG and ADC changes at day 14 (study primary endpoint), and no significant correlation with other ADC metrics. In scans acquired one week prior to surgery, there was no significant correlation between ADC metrics and percentage of viable tumour, percentage necrosis, percentage fibrosis, or Ki67 index. Conclusions: Our hypothesis was not supported by the data. The lack of meaningful correlation between change in ADC and TRG is a robust finding which is not explained by variability or small sample size. Change in ADC is not a proxy for TRG in metastatic colorectal cancer.

Funder

Innovative Medicines Initiative Joint Undertaking

European Union’s Seventh Framework Programme

EFPIA

European Organization for Research and Treatment of Cancer

European Society of Pathology

Sir Ronald Grierson

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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