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The prognostic role of variations in tumour markers (CEA CA15.3) in patients with metastatic breast cancer treated with CDK4/6 inhibitors

机译:肿瘤标志物 (CEACA15.3) 变化对 CDK4/6 抑制剂治疗转移性乳腺癌患者的预后作用

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摘要

Tumour markers have no established role in the monitoring of the course of metastatic breast cancer during antineoplastic therapy, yet cancer antigen 15.3 (CA15.3) and carcinoembryonic antigen (CEA) are commonly used in clinical practice to aid in the early detection of progression of disease (PD). In our multicentre, prospective, real-life study, we enrolled 142 consecutive patients with advanced breast cancer receiving endocrine therapy in combination with a CDK4/6 inhibitor from January 2017 to October 2020; 75 patients had PD at the time of database closure. We measured serum marker concentrations at regular 4-month intervals together with radiological tumour response assessments and in cases of clinical suspicion of PD. Appropriate descriptive and inferential statistical methods were used to analyse serum marker level trends amongst prespecified subgroups and at specific time points (baseline, best radiologically documented tumour response and first detection of PD) in the subpopulation of patients with PD at the time of database closure. Notably, the median time from treatment initiation to best tumour response was 4.4 months. We evaluated the presence of an association between baseline CA15.3 and CEA levels and prespecified clinical characteristics but found no clinically meaningful correlation. We assessed marker level variations at the time of best radiologically documented disease response and PD: in the subgroup of patients who responded to treatment before progressing, we detected a statistically significant correlation with tumour marker variation between the time of best response and progression; this finding was not confirmed in the subgroup of patients that did not benefit from treatment. In conclusion, serum tumour marker flares can be useful in the early diagnosis of PD but should not be used as the sole factor prompting a change in treatment strategy without radiological confirmation.
机译:在抗肿瘤治疗期间,肿瘤标志物在监测转移性乳腺癌的病程中没有确定的作用,但癌症抗原 15.3 (CA15.3) 和癌胚抗原 (CEA) 在临床实践中通常用于帮助早期发现疾病进展 (PD)。在我们的多中心、前瞻性、真实研究中,我们连续招募了 142 例在 2017 年 1 月至 2020 年 10 月期间接受内分泌治疗联合 CDK4/6 抑制剂的晚期乳腺癌患者;75 例患者在数据库关闭时患有 PD。我们定期测量 4 个月一次的血清标志物浓度,同时进行放射学肿瘤反应评估,并在临床怀疑 PD 的病例中测量。使用适当的描述性和推理性统计方法分析预先指定的亚组和特定时间点(基线、放射学记录的最佳肿瘤反应和 PD 的首次检测)的血清标志物水平趋势数据库关闭时 PD 患者亚群。值得注意的是,从治疗开始到最佳肿瘤反应的中位时间为 4.4 个月。我们评估了基线 CA15.3 和 CEA 水平与预先指定的临床特征之间存在关联,但没有发现具有临床意义的相关性。我们评估了放射学记录的最佳疾病反应和 PD 时的标志物水平变化: 在进展前对治疗有反应的患者亚组中,我们检测到最佳反应时间和进展之间的肿瘤标志物变化存在统计学上的显着相关性;这一发现在未从治疗中获益的患者亚组中未得到证实。总之,血清肿瘤标志物耀斑可用于 PD 的早期诊断,但不应作为未经放射学确认而改变治疗策略的唯一因素。

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