# False Liver Metastasis by Positron Emission Tomography/Computed Tomography Scan after Chemoradiotherapy for Esophageal Cancer—Potential Overstaged Pitfalls of Treatment

**Authors:** Sen-Ei Shai, Yi-Ling Lai, Chen-I Chang, Chi-Wei Hsieh

PMC · DOI: 10.3390/cancers16050948 · Cancers · 2024-02-26

## TL;DR

FDG PET-CT scans after esophageal cancer treatment can mistakenly show liver metastases due to radiation damage, leading to incorrect staging and treatment decisions.

## Contribution

Highlights the diagnostic challenge of distinguishing radiation-induced liver injury from true metastases using FDG PET-CT in esophageal cancer patients.

## Key findings

- Focal FDG uptake in the liver after CRT may indicate radiation-induced liver injury rather than metastasis.
- Combining imaging techniques and monitoring for resolution of abnormalities can help differentiate RILD from metastases.
- Overstaging due to RILD can lead to unnecessary exclusion of patients from curative surgery.

## Abstract

FDG PET-CT scans are critical in detecting metastases during neoadjuvant chemoradiotherapy for esophageal cancer, particularly for potential liver involvement. The liver’s proximity to the radiation field in distal esophageal cancer therapies raises the risk of radiation-induced liver damage. Therefore, greater FDG absorption in the liver does not always imply metastases; it could also signal radiation-induced damage, which is a concern for distal esophageal carcinoma therapies in the left hepatic lobe, potentially leading to overstaging. Accordingly, thorough monitoring of FDG activity in the liver is required to reliably distinguish between radiation effects and genuine distant metastases. If FDG activity is seen in the left or caudate liver lobes following CRT, additional diagnostic procedures are demanded to confirm or rule out distant metastases. Surgery, usually scheduled 6–8 weeks after CRT, should be followed by an FDG PET-CT scan to look for new interval metastases, as their existence may prohibit surgical intervention.

In patients with esophageal cancer undergoing neoadjuvant chemoradiotherapy (nCRT), subsequent restaging with F-18-fluorodeoxyglucose (18F-FDG) positron emission tomography–computed tomography (PET-CT) can reveal the presence of interval metastases, such as liver metastases, in approximately 10% of cases. Nevertheless, it is not uncommon in clinical practice to observe focal FDG uptake in the liver that is not associated with liver metastases but rather with radiation-induced liver injury (RILI), which can result in the overstaging of the disease. Liver radiation damage is also a concern during distal esophageal cancer radiotherapy due to its proximity to the left liver lobe, typically included in the radiation field. Post-CRT, if FDG activity appears in the left or caudate liver lobes, a thorough investigation is needed to confirm or rule out distant metastases. The increased FDG uptake in liver lobes post-CRT often presents a diagnostic dilemma. Distinguishing between radiation-induced liver disease and metastasis is vital for appropriate patient management, necessitating a combination of imaging techniques and an understanding of the factors influencing the radiation response. Diagnosis involves identifying new foci of hepatic FDG avidity on PET/CT scans. Geographic regions of hypoattenuation on CT and well-demarcated regions with specific enhancement patterns on contrast-enhanced CT scans and MRI are characteristic of radiation-induced liver disease (RILD). Lack of mass effect on all three modalities (CT, MRI, PET) indicates RILD. Resolution of abnormalities on subsequent examinations also helps in diagnosing RILD. Moreover, it can also help to rule out occult metastases, thereby excluding those patients from further surgery who will not benefit from esophagectomy with curative intent.

## Linked entities

- **Diseases:** esophageal cancer (MONDO:0007576)

## Full-text entities

- **Diseases:** False Liver Metastasis (MESH:D009362), Esophageal Cancer (MESH:D004938), Liver radiation damage (MESH:D007953)
- **Chemicals:** 18F-FDG (MESH:D019788)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC10931232/full.md

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Source: https://tomesphere.com/paper/PMC10931232