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Comparison of [18F]FDG and [68 Ga]pentixafor PET/CT in Nasopharyngeal Carcinoma

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Abstract

Purpose

This study aimed to explore the feasibility of [68 Ga]pentixafor positron emission tomography/computed tomography (PET/CT) in patients with nasopharyngeal carcinoma (NPC).

Procedures

This prospective study included patients with NPC who underwent [68 Ga]pentixafor PET/CT and 2-[18F]fuoro-2-deoxy-D-glucose ([18F]FDG) PET/CT within one week between November 2022 and March 2023. The [68 Ga]pentixafor and [18F]FDG uptakes in primary and metastatic lesions were measured and compared.

Results

Twenty-five participants (21 patients for initial stage and four patients for recurrence detection) were enrolled in our study. The participants underwent [18F]FDG PET/CT and [68 Ga]pentixafor PET/CT. [68 Ga]pentixafor PET/CT had the same detection rate as [18F]FDG for primary tumor (96% vs. 96%). The [68 Ga]pentixafor maximum standard uptake value (SUVmax) and target-to-background ratio (TBR) of primary tumors were lower than those of [18F]FDG (SUVmax: 8.13 ± 2.78 vs. 14.25 ± 6.45; P < 0.01; TBR: 5.17 ± 2.14 vs. 9.81 ± 5.30, P < 0.01). The difference between tumor volume of [68 Ga]pentixafor (TVpentixafor) and tumor volume of [18F]FDG (TVFDG) showed no significance (median: 16.01 vs. 9.56, P = 0.332). In the detection of suspected metastatic cervical lymph nodes (CLNs), [68 Ga]pentixafor PET possessed a lower SUVmax than [18F]FDG PET/CT (SUVmax: 6.86 ± 2.63 vs. 10.39 ± 5.28, P < 0.01), but there was no significant difference in the detection rate between [68 Ga]pentixafor and [18F]FDG PET/CT (96 vs. 98, P = 0.613).

Conclusions

[68 Ga]pentixafor is a promising imaging tracer for detecting primary and metastatic NPC. [68 Ga]pentixafor PET/CT is comparable to [18F]FDG PET/CT in the detection rate of primary tumors and metastatic cervical lymph nodes in nasopharyngeal carcinoma, but [68 Ga]pentixafor uptake was heterogeneous. [68 Ga]pentixafor PET/CT may help select patients most likely to benefit from CXCR4-directed endoradiotherapy.

Clinical trial registration No.: ChiCTR2200065902

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Acknowledgements

We would like to thank Yue Feng, Department of Nuclear Medicine, the Affiliated Hospital of Southwest Medical University, for preparation of [68Ga]pentixafor.

Funding

This study was funded by Sichuan Provincial Science and Technology Department (Grant No.2022NSFSC0827), Luzhou Science and Technology Bureau (Grant No.2021CDLZ-9) and Sichuan Science and Technology Program (Grant No.2022YFS0608).

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Authors and Affiliations

Authors

Contributions

ML, XC and HD contributed to the study conception and design. Material preparation and data collection were performed by ML, XC, HD, QS, YZ, YC and LC. ML and XC processed and analyzed the data. The first draft of the manuscript was written by ML and XC, and HD reviewed and revised the manuscript. All authors contributed to the article and approved the submitted version.

Corresponding authors

Correspondence to Yun Zheng or Liang Cai.

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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

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Informed consent was obtained from all individual participants included in the study.

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The authors declare that they have no conflict of interest.

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Mengna Liu, Xi Chen and Haoyuan Ding contributed equally to this work and share first authorship.

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Liu, M., Chen, X., Ding, H. et al. Comparison of [18F]FDG and [68 Ga]pentixafor PET/CT in Nasopharyngeal Carcinoma. Mol Imaging Biol (2024). https://doi.org/10.1007/s11307-024-01913-1

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