Association of FTH1-Expressing Circulating Tumor Cells With Efficacy of Neoadjuvant Chemotherapy for Patients With Breast Cancer: A Prospective Cohort Study.
Association of FTH1-Expressing Circulating Tumor Cells With Efficacy of Neoadjuvant Chemotherapy for Patients With Breast Cancer: A Prospective Cohort Study.
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表达fth1的循环肿瘤细胞与乳腺癌患者新辅助化疗疗效的关联:一项前瞻性队列研究
DOI:
10.1093/oncolo/oyad195
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发表时间:
2024-01-05
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影响因子:
--
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中科院分区:
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The association between different phenotypes and genotypes of circulating tumor cells (CTCs) and efficacy of neoadjuvant chemotherapy (NAC) remains uncertain. This study was conducted to evaluate the relationship of FTH1 gene-associated CTCs (F-CTC) with/without epithelial-mesenchymal transition (EMT) markers, or their dynamic changes with the efficacy of NAC in patients with non-metastatic breast cancer. This study enrolled 120 patients with non-metastatic breast cancer who planned to undergo NAC. The FTH1 gene and EMT markers in CTCs were detected before NAC (T0), after 2 cycles of chemotherapy (T1), and before surgery (T2). The associations of these different types of CTCs with rates of pathological complete response (pCR) and breast-conserving surgery (BCS) were evaluated using the binary logistic regression analysis. F-CTC in peripheral blood ≥1 at T0 was an independent factor for pCR rate in patients with HER2-positive (odds ratio [OR]=0.08, 95% confidence interval [CI], 0.01-0.98, P = .048). The reduction in the number of F-CTC at T2 was an independent factor for BCS rate (OR = 4.54, 95% CI, 1.14-18.08, P = .03). The number of F-CTC prior to NAC was related to poor response to NAC. Monitoring of F-CTC may help clinicians formulate personalized NAC regimens and implement BCS for patients with non-metastatic breast cancer. This article assesses the associations of different types of circulating tumor cells and their dynamic changes with the efficacy of neoadjuvant chemotherapy in patients with non-metastatic breast cancer.
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影响因子:
5.6
作者:
Lu B;Chen XB;Ying MD;He QJ;Cao J;Yang B
通讯作者:
Yang B
DOI:
10.1074/mcp.m113.037176
发表时间:
2014-07
期刊:
Molecular & cellular proteomics : MCP
影响因子:
--
作者:
Liu NQ;De Marchi T;Timmermans AM;Beekhof R;Trapman-Jansen AM;Foekens R;Look MP;van Deurzen CH;Span PN;Sweep FC;Brask JB;Timmermans-Wielenga V;Debets R;Martens JW;Foekens JA;Umar A
通讯作者:
Umar A
影响因子:
3.4
作者:
Kanojia, Deepak;Zhou, Weidong;Chen, Hexin
通讯作者:
Chen, Hexin
影响因子:
44.1
作者:
Tang D;Chen X;Kang R;Kroemer G
通讯作者:
Kroemer G
影响因子:
3.8
作者:
Gorges TM;Tinhofer I;Drosch M;Röse L;Zollner TM;Krahn T;von Ahsen O
通讯作者:
von Ahsen O