The efficiency of 18F-FDG PET-CT for predicting the major pathologic response to the neoadjuvant PD-1 blockade in resectable non-small cell lung cancer
Autor: | Zewei Zhang, Shugeng Gao, Xiuli Tao, Jie Wang, Ning Wu, Shuhang Wang, Wei Tang, Jie He, Jianming Ying, Zhijie Wang, Ning Li, Yun Ling |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
Lung Neoplasms medicine.medical_treatment Programmed Cell Death 1 Receptor Progressive Metabolic Disease Gastroenterology 030218 nuclear medicine & medical imaging Surgical pathology 03 medical and health sciences 0302 clinical medicine Non-small cell lung cancer Major Pathologic Response Fluorodeoxyglucose F18 Internal medicine Carcinoma Non-Small-Cell Lung Positron Emission Tomography Computed Tomography Biopsy medicine Humans Radiology Nuclear Medicine and imaging Stage (cooking) Lung cancer Pathological Neoadjuvant therapy medicine.diagnostic_test business.industry 18F-FDG PET-CT General Medicine medicine.disease Pathologic response 030220 oncology & carcinogenesis Original Article business Checkpoint inhibitors |
Zdroj: | European Journal of Nuclear Medicine and Molecular Imaging |
ISSN: | 1619-7089 1619-7070 |
Popis: | Purpose Investigate whether 18F-FDG PET-CT has the potential to predict the major pathologic response (MPR) to neoadjuvant sintilimab in resectable NSCLC patients, and the potential of sifting patients who probably benefit from immunotherapy. Methods Treatment-naive patients with resectable NSCLC (stage IA–IIIB) received two cycles of sintilimab (200 mg, intravenously, day 1 and 22). Surgery was performed between day 29 and 43. PET-CT was obtained at baseline and prior to surgery. The following lean body mass–corrected metabolic parameters were calculated by PET VCAR: SULmax, SULpeak, MTV, TLG, ΔSULmax%, ΔSULpeak%, ΔMTV%, ΔTLG%. PET responses were classified using PERCIST. The above metabolic information on FDG-PET was correlated with the surgical pathology. (Registration Number: ChiCTR-OIC-17013726). Results Thirty-six patients received 2 doses of sintilimab, all of whom underwent PET-CT twice and had radical resection (35) or biopsy (1). MPR occurred in 13 of 36 resected tumors (36.1%, 13/36). The degree of pathological regression was positively correlated with SULmax (p = 0.036) of scan-1, and was negatively correlated with all metabolic parameters of scan-2, and the percentage changes of the metabolic parameters after neoadjuvant therapy (p peak% Conclusions 18F-FDG PET-CT can predict MPR to neoadjuvant sintilimab in resectable non-small cell lung cancer. |
Databáze: | OpenAIRE |
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