Prognostic significance of circulating tumor cell measurement in the peripheral blood of patients with nasopharyngeal carcinoma
Autor(a) principal: | |
---|---|
Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , |
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 |