# Combination of Ethoxybenzyl‐Diethylenetriamine Pentaacetic Acid‐Enhanced Magnetic Resonance Imaging and a Serum Biomarker Is Useful in the Diagnosis of Hepatic Sinusoidal Disorder After Chemotherapy Treatment

**Authors:** Tomonari Shimagaki, Keishi Sugimachi, Takahiro Tomino, Takeshi Kurihara, Emi Onishi, Yutaro Shimomura, Kenji Shinozaki, Masaru Morita

PMC · DOI: 10.1002/ags3.70092 · 2025-09-09

## TL;DR

Combining a specific MRI technique and a blood test helps detect liver damage after chemotherapy in colorectal cancer patients, improving diagnosis and surgical planning.

## Contribution

The study introduces a non-invasive diagnostic method combining EOB-MRI and APRI for detecting SOS in CRLM patients.

## Key findings

- 25 out of 70 patients treated with oxaliplatin showed blue liver during surgery.
- EOB-MRI and APRI scores were significantly higher in patients with blue liver.
- The combination of EOB-MRI and APRI achieved 78% sensitivity and 67.7% specificity for blue liver detection.

## Abstract

Sinusoidal obstruction syndrome (SOS), also known as “blue liver (BL),” is a common hepatic injury following oxaliplatin‐based chemotherapy in patients with colorectal liver metastases (CRLM). Early non‐invasive identification of SOS is essential for safe hepatic resection and improved outcomes; however, this remains clinically challenging.

We retrospectively analyzed 155 patients who underwent preoperative ethoxybenzyl‐diethylenetriamine pentaacetic acid‐enhanced magnetic resonance imaging (EOB‐MRI) and hepatic resection for CRLM between 2014 and 2022. Radiologists evaluated SOS on EOB‐MRI using a five‐point reticular signal grading scale. Aspartate aminotransferase to platelet ratio index (APRI) scores were calculated preoperatively. BL was confirmed intraoperatively based on characteristic liver discoloration. Correlations between EOB‐MRI scores, APRI, and clinical outcomes were analyzed using receiver operating characteristic curves, survival analysis, and multivariate statistics.

Of 70 patients treated with preoperative oxaliplatin, 25 (35.7%) exhibited intraoperative BL. Overall survival was significantly worse in the blue liver group (p = 0.0338), although disease‐free survival did not differ significantly. Patients in the BL group had significantly higher APRI and EOB‐MRI scores (p = 0.0028 and p < 0.0001, respectively). The combined EOB‐MRI assessment and APRI had the highest diagnostic ability for BL detection, yielding an area under the curve of 0.806, with 78.0% sensitivity and 67.7% specificity. Patients with high scores in both modalities exhibited significantly poorer overall survival.

A combination of EOB‐MRI and APRI is a valuable non‐invasive tool for preoperative detection of SOS in patients with CRLM. This approach improves diagnostic accuracy, facilitates surgical planning, and may predict long‐term prognosis following hepatic resection.

ROC analyses of APRI score, EOB‐MRI, and a combination of EOB‐MRI and APRI score for blue liver.

## Linked entities

- **Chemicals:** oxaliplatin (PubChem CID 9887053)
- **Diseases:** sinusoidal obstruction syndrome (MONDO:0019514)

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, XYLT2 (xylosyltransferase 2) [NCBI Gene 64132] {aka PXYLT2, SOS, XT-II, XT2, xylT-II}, GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** hematologic (MESH:D006402), hypersplenism (MESH:D006971), CRC (MESH:D015179), viral hepatitis (MESH:D014777), portal hypertension (MESH:D006975), ascites (MESH:D001201), CRLM (MESH:D009362), wound infection (MESH:D014946), deep vein thrombosis (MESH:D020246), CD (MESH:D003424), postoperative complications (MESH:D011183), thrombocytopenia (MESH:D013921), bone marrow suppression (MESH:D001855), and hepatocellular injury (MESH:D056486), BL (MESH:D017093), autoimmune hepatitis (MESH:D019693), liver cancer (MESH:D006528), primary biliary cholangitis (MESH:D008105), sinusoidal endothelial injury (MESH:D000094724), hepatic dysfunction (MESH:D008107), inflammation (MESH:D007249), pulmonary infection (MESH:D012141), fibrosis (MESH:D005355), liver fibrosis (MESH:D008103), metastatic (MESH:D000092182), blood loss (MESH:D016063), atrophy (MESH:D001284), Cancer (MESH:D009369), delirium (MESH:D003693), venous congestion (MESH:D006940), splenomegaly (MESH:D013163), esophageal or gastric varices (MESH:D004932), SOS (MESH:D006504), RLS (MESH:C538361)
- **Chemicals:** EOB (-), ICG (MESH:D007208), Cr (MESH:D002857), creatinine (MESH:D003404), Gd-EOB-DTPA (MESH:C073590), bilirubin (MESH:D001663), oxaliplatin (MESH:D000077150)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12962010/full.md

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Source: https://tomesphere.com/paper/PMC12962010