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Published on: July 21, 2018
Different detection rates of brain metastasis in different pathological types of lung cancer by 18F-FAPI PET/CT
Haoqian Li1, Pei Li2, Shouhui Zhu1
1Department of Radiology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Background:
The purpose of this study was to evaluate the utility of fluorine-18-fibroblast activation protein inhibitor (18F-FAPI) PET/CT for detecting brain metastasis (BM) in different pathological types of lung cancer using craniocerebral MRI as the standard.
Methods:
From December 2020 to October 2021, patients with pathologically confirmed lung cancer and suspected BM were prospectively enrolled and underwent paired 18F-FAPI PET/CT and MRI. The number of BMs and maximum tumor diameter were measured by MRI. The maximum and peak standardized uptake values (SUVmax and SUVpeak, respectively) and tumor-to-background ratio (TBR) on 18F-FAPI PET/CT in BMs were evaluated.
Results:
A total of 76 BM lesions from 18 patients (11 males and 7 females) were evaluated. Among these, 23 lesions were detected by 18F-FAPI PET/CT. The detection rate of BM in adenocarcinoma was 48.28%, which was significantly higher than that in large cell carcinoma (16.67%, P = 0.016) and small cell carcinoma (0%, P = 0.009), but showed no significant difference from that in squamous carcinoma (35.71%, P = 0.437). The detection rate in squamous carcinoma was significantly higher than that in small cell carcinoma (P = 0.043), while no significant differences were observed between large cell carcinoma and small cell carcinoma (P = 0.183), or between large cell carcinoma and squamous carcinoma (P = 0.191).
Conclusions:
This study revealed differences in the detection rates of BM in lung cancer types by 18F-FAPI PET/CT, with the highest and lowest detection rates in adenocarcinoma and small cell carcinoma, respectively, which may be valuable for predicting the prognosis of lung cancer patients with BM.
Trial Registration:
Institutional review board approval NO. SDZLEC2021-112-02.
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