Abstract 885P
Background
This study aimed to investigate the feasibility of using ligand-targeted polymerase chain reaction (LT-PCR) to detect folate receptor-positive circulating tumor cells (FR+CTCs) and their potential role as an auxiliary marker for diagnosis and treatment monitoring in nasopharyngeal carcinoma (NPC).
Methods
This was a single-center, prospective, non-interventional clinical study at Fujian Cancer Hospital. The study included newly diagnosed nasopharyngeal carcinoma patients with at least one measurable lesion and a benign control group. Patients underwent comprehensive treatment based on radical radiotherapy, and the level of FR+CTC was dynamically detected after treatment. FR+CTC was quantitated using ligand-targeted PCR and verified using immunofluorescence. The ROC curve was used to determine specificity and sensitivity thresholds, and the AUC was calculated. Comparisons between groups were performed using statistical tests, and p < 0.05 was considered statistically significant.
Results
A total of 254 subjects were included in the study, including 145 newly diagnosed NPC patients and 109 healthy volunteers. The study found that the level of FR+CTC was significantly higher in NPC patients than in healthy individuals, and the levels were also higher in stage III and IV patients. The FR+CTC detection method had a higher AUC, and the cut-off value between the NPC and control groups was 9.380 FU/3ml, with a sensitivity of 99.1% and a specificity of 79.2%. The study also found that FR+CTC levels were associated with gender, age, TNM stage, and MPTD, but not with the level of EB-DNA. After radiotherapy, most patients showed a significant decrease in FR+CTC levels, indicating the potential of FR+CTC as a dynamic biomarker for monitoring treatment response in NPC.
Conclusions
This study demonstrates that LT-PCR technology can accurately detect FR+CTCs in NPC patients. FR+CTC has the potential to be used not only as an auxiliary biomarker for early detection and diagnosis of nasopharyngeal carcinoma, but also as a potential marker for dynamic assessment and monitoring of disease progression, recurrence, and metastasis.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
910P - Machine learning-based survival prediction model for postoperative parotid mucoepidermoid carcinoma
Presenter: Chen Zihan
Session: Poster session 12
911P - Post-radiotherapy (RT) Epstein-Barr virus (EBV) DNA dynamics identifies optimal timepoint for stratification of high-risk nasopharyngeal carcinoma (NPC)
Presenter: Janice Ser Huey Tan
Session: Poster session 12
912P - Toripalimab in combination with anlotinib in previously treated recurrent or metastatic nasopharyngeal carcinoma: The interim analysis of the single-arm, phase II TORAL study
Presenter: QingQing Cai
Session: Poster session 12
916P - Reducing radiation-induced temporal lobe injury by changing tumor prescription dose in nasopharyngeal carcinoma
Presenter: Xiao Xiao
Session: Poster session 12
917P - Radiation-induced nasopharyngeal necrosis in locally-recurrent nasopharyngeal carcinoma patients after re-radiotherapy
Presenter: Runda Huang
Session: Poster session 12
918P - SPP1-related M2 macrophage signatures predict prognosis and immunotherapy response in patients with nasopharyngeal carcinoma
Presenter: Li Ying
Session: Poster session 12
919P - A prognostic model of nasopharyngeal carcinoma based on 18F-FDG PET-CT radiomic parameters and clinical characteristics of patients
Presenter: Wu xi
Session: Poster session 12
920P - Envafolimab plus chemoradiotherapy for locally advanced nasopharyngeal carcinoma (NPC), a prospective, single-armed phase II trial
Presenter: Xiaohui Wang
Session: Poster session 12
921P - HB-200 arenavirus-based immunotherapy plus pembrolizumab as a first-line treatment of patients with recurrent/metastatic HPV16 positive head and neck cancer
Presenter: Lisle Nabell
Session: Poster session 12