Prognostic significance of circulating tumor cell measurement in the peripheral blood of patients with nasopharyngeal carcinoma

Detalhes bibliográficos
Autor(a) principal: Gao, Tinghua
Data de Publicação: 2023
Outros Autores: Mao, Jinxing, Huang, Jindu, Luo, Fengling, Lin, Lixiang, Lian, Yingni, Bin, Sanmei, Zhao, Lianghua, Li, Shuping
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/213711
Resumo: Objective: Nasopharyngeal Carcinoma (NPC) is lethal cancer. Typically, relapse and metastasis are the outcomes of most patients. Against this backdrop, this study aimed to investigate the correlation between Circulating Tumor Cell (CTC) profiles and clinicopathological features in patients with NPC. Patients and methods: A total of 119 blood samples from 79 patients were collected from patients with NPC during treatment. CanPatrolTM CTC enrichment and RNA In Situ Hybridization (RNA-ISH) were used to characterize CTCs, including epithelial, Mesenchymal (MCTCs), and epithelial/mesenchymal mixed types according to their surface markers. Results: The number of CTCs and MCTCs in the pre-treatment group was significantly higher than that in the post-treatment group (p < 0.05). The total number of CTCs and MCTCs cell numbers was significant correlation with Tumor-Node-Metastasis (TNM) staging (p < 0.05), Progression-Free Survival (PFS), and Overall Survival (OS). The PFS of patients with > 7 CTCs or > 5 MCTCs per 5 mL blood was significantly shorter PFS than those patients with ≤ 7 CTCs or ≤ 5 MCTCs (p < 0.05). Patients treated with targeted therapy combined with chemoradiotherapy had poorer PFS and OS rates than those treated with chemoradiotherapy (p < 0.05). The Kaplan-Meier survival analysis also demonstrated that patients with changes in CTC > 4 were strongly associated with PFS and OS rates (p < 0.05). Conclusion: CTC and MCTC number detection in patients with NPC is a useful biomarker for predicting patient progress. Patients with more than 7 CTCs or 5 MCTCs in 5 mL of blood had shorter PFS and OS rates. CTC and MCTC count changes were also significantly associated with the patient's therapy.
id USP-19_9afd002f36a9a76ce132569a9ba58537
oai_identifier_str oai:revistas.usp.br:article/213711
network_acronym_str USP-19
network_name_str Clinics
repository_id_str
spelling Prognostic significance of circulating tumor cell measurement in the peripheral blood of patients with nasopharyngeal carcinomaNasopharyngeal carcinomaCirculating tumor cellsClinical pathological featuresTreatmentObjective: Nasopharyngeal Carcinoma (NPC) is lethal cancer. Typically, relapse and metastasis are the outcomes of most patients. Against this backdrop, this study aimed to investigate the correlation between Circulating Tumor Cell (CTC) profiles and clinicopathological features in patients with NPC. Patients and methods: A total of 119 blood samples from 79 patients were collected from patients with NPC during treatment. CanPatrolTM CTC enrichment and RNA In Situ Hybridization (RNA-ISH) were used to characterize CTCs, including epithelial, Mesenchymal (MCTCs), and epithelial/mesenchymal mixed types according to their surface markers. Results: The number of CTCs and MCTCs in the pre-treatment group was significantly higher than that in the post-treatment group (p < 0.05). The total number of CTCs and MCTCs cell numbers was significant correlation with Tumor-Node-Metastasis (TNM) staging (p < 0.05), Progression-Free Survival (PFS), and Overall Survival (OS). The PFS of patients with > 7 CTCs or > 5 MCTCs per 5 mL blood was significantly shorter PFS than those patients with ≤ 7 CTCs or ≤ 5 MCTCs (p < 0.05). Patients treated with targeted therapy combined with chemoradiotherapy had poorer PFS and OS rates than those treated with chemoradiotherapy (p < 0.05). The Kaplan-Meier survival analysis also demonstrated that patients with changes in CTC > 4 were strongly associated with PFS and OS rates (p < 0.05). Conclusion: CTC and MCTC number detection in patients with NPC is a useful biomarker for predicting patient progress. Patients with more than 7 CTCs or 5 MCTCs in 5 mL of blood had shorter PFS and OS rates. CTC and MCTC count changes were also significantly associated with the patient's therapy.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2023-03-23info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/21371110.1016/j.clinsp.2023.100179Clinics; Vol. 78 (2023); 100179Clinics; v. 78 (2023); 100179Clinics; Vol. 78 (2023); 1001791980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/213711/195834Copyright (c) 2023 Clinicsinfo:eu-repo/semantics/openAccessGao, TinghuaMao, JinxingHuang, JinduLuo, FenglingLin, LixiangLian, YingniBin, SanmeiZhao, LianghuaLi, Shuping2023-07-06T13:05:38Zoai:revistas.usp.br:article/213711Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2023-07-06T13:05:38Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Prognostic significance of circulating tumor cell measurement in the peripheral blood of patients with nasopharyngeal carcinoma
title Prognostic significance of circulating tumor cell measurement in the peripheral blood of patients with nasopharyngeal carcinoma
spellingShingle Prognostic significance of circulating tumor cell measurement in the peripheral blood of patients with nasopharyngeal carcinoma
Gao, Tinghua
Nasopharyngeal carcinoma
Circulating tumor cells
Clinical pathological features
Treatment
title_short Prognostic significance of circulating tumor cell measurement in the peripheral blood of patients with nasopharyngeal carcinoma
title_full Prognostic significance of circulating tumor cell measurement in the peripheral blood of patients with nasopharyngeal carcinoma
title_fullStr Prognostic significance of circulating tumor cell measurement in the peripheral blood of patients with nasopharyngeal carcinoma
title_full_unstemmed Prognostic significance of circulating tumor cell measurement in the peripheral blood of patients with nasopharyngeal carcinoma
title_sort Prognostic significance of circulating tumor cell measurement in the peripheral blood of patients with nasopharyngeal carcinoma
author Gao, Tinghua
author_facet Gao, Tinghua
Mao, Jinxing
Huang, Jindu
Luo, Fengling
Lin, Lixiang
Lian, Yingni
Bin, Sanmei
Zhao, Lianghua
Li, Shuping
author_role author
author2 Mao, Jinxing
Huang, Jindu
Luo, Fengling
Lin, Lixiang
Lian, Yingni
Bin, Sanmei
Zhao, Lianghua
Li, Shuping
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Gao, Tinghua
Mao, Jinxing
Huang, Jindu
Luo, Fengling
Lin, Lixiang
Lian, Yingni
Bin, Sanmei
Zhao, Lianghua
Li, Shuping
dc.subject.por.fl_str_mv Nasopharyngeal carcinoma
Circulating tumor cells
Clinical pathological features
Treatment
topic Nasopharyngeal carcinoma
Circulating tumor cells
Clinical pathological features
Treatment
description Objective: Nasopharyngeal Carcinoma (NPC) is lethal cancer. Typically, relapse and metastasis are the outcomes of most patients. Against this backdrop, this study aimed to investigate the correlation between Circulating Tumor Cell (CTC) profiles and clinicopathological features in patients with NPC. Patients and methods: A total of 119 blood samples from 79 patients were collected from patients with NPC during treatment. CanPatrolTM CTC enrichment and RNA In Situ Hybridization (RNA-ISH) were used to characterize CTCs, including epithelial, Mesenchymal (MCTCs), and epithelial/mesenchymal mixed types according to their surface markers. Results: The number of CTCs and MCTCs in the pre-treatment group was significantly higher than that in the post-treatment group (p < 0.05). The total number of CTCs and MCTCs cell numbers was significant correlation with Tumor-Node-Metastasis (TNM) staging (p < 0.05), Progression-Free Survival (PFS), and Overall Survival (OS). The PFS of patients with > 7 CTCs or > 5 MCTCs per 5 mL blood was significantly shorter PFS than those patients with ≤ 7 CTCs or ≤ 5 MCTCs (p < 0.05). Patients treated with targeted therapy combined with chemoradiotherapy had poorer PFS and OS rates than those treated with chemoradiotherapy (p < 0.05). The Kaplan-Meier survival analysis also demonstrated that patients with changes in CTC > 4 were strongly associated with PFS and OS rates (p < 0.05). Conclusion: CTC and MCTC number detection in patients with NPC is a useful biomarker for predicting patient progress. Patients with more than 7 CTCs or 5 MCTCs in 5 mL of blood had shorter PFS and OS rates. CTC and MCTC count changes were also significantly associated with the patient's therapy.
publishDate 2023
dc.date.none.fl_str_mv 2023-03-23
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/213711
10.1016/j.clinsp.2023.100179
url https://www.revistas.usp.br/clinics/article/view/213711
identifier_str_mv 10.1016/j.clinsp.2023.100179
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/213711/195834
dc.rights.driver.fl_str_mv Copyright (c) 2023 Clinics
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2023 Clinics
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 78 (2023); 100179
Clinics; v. 78 (2023); 100179
Clinics; Vol. 78 (2023); 100179
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
_version_ 1800222767131394048