Evidence map›Paper›PMID 39302034›Full record

ArticleCancer medicine2024

Combination of circulating tumor cells and 18F-FDG PET/CT for precision diagnosis in patients with non-small cell lung cancer.

Momo Sun, Dongyan Lu, Xiaoping Li, Jin Wang, Liang Zhang, Pan Yang, Yang Yang, Jie Shen

Abstract read
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Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Momo SunThe First Central Clinical School, Tianjin Medical University, Tianjin, China.
Dongyan LuThe First Central Clinical School, Tianjin Medical University, Tianjin, China.
Xiaoping LiDepartment of Thoracic Surgery, Tianjin First Central Hospital, Tianjin, China.
Jin WangThe First Central Clinical School, Tianjin Medical University, Tianjin, China.
Liang ZhangDepartment of Thoracic Surgery, Tianjin First Central Hospital, Tianjin, China.
Pan YangDepartment of Thoracic Surgery, Tianjin First Central Hospital, Tianjin, China.
Yang YangThe First Central Clinical School, Tianjin Medical University, Tianjin, China.
Jie ShenThe First Central Clinical School, Tianjin Medical University, Tianjin, China.

Funding

Study on nuclide nanoprobes with aggregation-induced luminescence properties in the integration of diagnosis and treatment of atherosclerotic vulnerable plaque in rabbits 21JCYBJC01060
6 · The paper itself

Abstract

purposeTo investigate the value of 2-deoxy-18f-fluorodeoxyglucose (18F-FDG) positron emission tomography/computed tomography (PET/CT) and circulating tumor cells (CTCs) for the differential diagnosis of patients with benign lung diseases and those with NSCLC. To explore the phenotypic heterogeneity of CTCs and their correlation with FDG uptake in patients with Stage I-IV NSCLC.

methodsBlood specimens from patients with benign lung diseases and patients with primary NSCLC were collected for the detection of CTCs and their subtypes (epithelial, mixed, and mesenchymal) and analyzed for 18F-FDG PET/CT tumor metabolic parameters, including the maximum standardized uptake value (SUV

resultsThere were a total of 65 patients with pulmonary diseases, including 12 patients with benign pulmonary diseases and 53 patients with NSCLC. The mean age was 67 ± 10 (38-89 years), 27 were females and 38 were males. 31 (22 males and 9 females) had a long history of smoking. The mean size of the largest diameter of all single lesions was 36 ± 22 mm with a range of 10-108 mm. Seven out of 12 benign diseases were inflammatory granulomatous lesions and 5 were inflammatory pseudotumours. Twenty-four out of 53 NSCLC were adenocarcinomas and 29 were squamous carcinomas. Twelve out of 53 patients with NSCLC were in Stage I, 10 were in Stage II, 17 were in Stage III and 14 were in Stage IV. SUV

conclusionBoth FDG PET metabolic parameters and CTCs demonstrated diagnostic value for NSCLC, and combining TLG with mixed CTCs could enhance their diagnostic efficacy. The total CTCs and mixed CTCs showed greater diagnostic value than FDG PET in distinguishing benign lesions from Stage I NSCLC. In NSCLC patients, the epithelial CTCs exhibited a positive correlation with SUV

Indexed as

Carcinoma, Non-Small-Cell LungFluorodeoxyglucose F18Lung NeoplasmsNeoplastic Cells, CirculatingPositron Emission Tomography Computed TomographyAdultAgedAged, 80 and overDiagnosis, DifferentialFemaleHumansMaleMiddle AgedNeoplasm StagingRadiopharmaceuticalsFluorodeoxyglucose F18Radiopharmaceuticals18F‐FDG PET/CTcirculating tumor cells (CTCs)diagnosisnon‐small‐cell lung cancer (NSCLC)

Identifiers

PMID39302034
PMCPMC11413915

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