Baa Annie Kanchan, Sharma Atul, Bhaskar Suman, Biswas Ahitagni, Thakar Alok, Kumar Rajeev, Jayant Sreeja, Aland Gourishankar, D'Souza Alain, Jadhav Vikas, Bharde Atul, Khandare Jayant, Pramanik Raja
Department of Medical Oncology, Dr B. R.A. Institute Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi 110 029, India.
Department of Radiation Oncology, Dr B. R.A. Institute Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi 110 029, India.
Ecancermedicalscience. 2023 Jul 20;17:1578. doi: 10.3332/ecancer.2023.1578. eCollection 2023.
Liquid biopsy is emerging as a non-invasive tool, providing a personalized snapshot of a primary and metastatic tumour. It aids in detecting early metastasis, recurrence or resistance to the disease. We aimed to assess the role of circulating tumour cells (CTCs) as a predictive biomarker in recurrent/metastatic head and neck cancer (head and neck squamous cell carcinoma (HNSCC)).
Thirty-five patients receiving palliative chemotherapy underwent blood sampling [2 mL in Ethylenediaminetetraacetic acid (EDTA) vial] at baseline and at 3 months intervals. The CTCs were isolated and evaluated using anti-epithelial cell adhesion molecule antibody-based enrichment using the OncoDiscover platform.
CTCs isolated from 80% of patients ( = 28) showed the sensitivity of cell detection at the baseline and 3 months intervals. The median CTC count was 1/1.5 mL of blood and the concordance with clinic-radiological outcomes was 51.4%. The median CTC count (1 (range:0-4) to 0 (range:0-1)) declined at 3 months in responders, while the non-responders had an increase in levels (0 (range :0-2) to 1 (range :0-3)). Although CTCs positively correlated with progression-free survival (PFS) and overall survival (OS), the association of CTCs did not show a significant difference with these parameters (PFS: 6 months versus 4 months; hazard ratio: 0.68; 95% confidence interval (CI): 0.29-1.58, = 0.323; OS: 10 months versus 8 months; hazard ratio: 0.54; 95% (CI):0.18-1.57 = 0.216) between CTC positive and CTC negative patients at 3 months.
This study highlights the utility of CTC as a disease progression-monitoring tool in recurrent HNSCC patients. Our findings suggest the potential clinical utility of CTC and the need for exploration in upfront settings of the disease as well (NCT: CTRL/2020/02/023378).
液体活检正成为一种非侵入性工具,可提供原发性和转移性肿瘤的个性化概况。它有助于检测疾病的早期转移、复发或耐药性。我们旨在评估循环肿瘤细胞(CTC)作为复发/转移性头颈癌(头颈部鳞状细胞癌(HNSCC))预测生物标志物的作用。
35例接受姑息化疗的患者在基线和每隔3个月时进行血样采集(在乙二胺四乙酸(EDTA)试管中采集2 mL血液)。使用OncoDiscover平台,基于抗上皮细胞粘附分子抗体富集法分离并评估CTC。
从80%的患者(n = 28)中分离出的CTC在基线和每隔3个月时显示出细胞检测的敏感性。CTC计数中位数为每1.5 mL血液中1个,与临床放射学结果的一致性为51.4%。有反应者在3个月时CTC计数中位数(从每1.5 mL血液中1个(范围:0 - 4)降至0个(范围:0 - 1))下降,而无反应者水平升高(从每1.5 mL血液中0个(范围:0 - 2)升至1个(范围:0 - 3))。尽管CTC与无进展生存期(PFS)和总生存期(OS)呈正相关,但在3个月时,CTC阳性和阴性患者之间,CTC与这些参数的关联未显示出显著差异(PFS:6个月对4个月;风险比:0.68;95%置信区间(CI):0.29 - 1.58,P = 0.323;OS:10个月对8个月;风险比:0.54;95%(CI):0.18 - 1.57,P = 0.216)。
本研究强调了CTC作为复发HNSCC患者疾病进展监测工具的实用性。我们的研究结果表明CTC具有潜在的临床应用价值,并且在该疾病的初始阶段也需要进行探索(临床试验注册号:CTR/2020/02/023378)。