Faculty of Medicine and Health Technology, Tampere University, Arvo Ylpön katu 34, 33520 Tampere, Finland.
Department of Oncology: Tays Cancer Center, Tampere University Hospital, Teiskontie 35, 33520 Tampere, Finland.
Int J Mol Sci. 2023 Apr 4;24(7):6753. doi: 10.3390/ijms24076753.
Serum carcinoembryonic antigen (CEA) is frequently monitored to detect colorectal cancer (CRC) recurrence after surgery. The clinical significance of transiently increased CEA during adjuvant chemotherapy is poorly understood. Serum CEA, CA19-9, CRP, YKL-40, and IL-6 were measured before, during, and after adjuvant 5-fluorouracil-based chemotherapy in the randomised LIPSYT study population. The biomarker kinetic patterns were classified into three groups: no increase, a transient increase (≥10% increase followed by a decrease), and a persistent increase during the adjuvant treatment, and the associations of these patterns with disease free-survival (DFS) and overall survival (OS) were investigated by using Cox regression analyses. The findings were validated in two single-centre cohorts that received modern adjuvant chemotherapy. A transient increase in CEA occurred in about a half of the patients during chemotherapy, in all the cohorts. The patients with a transient increase had a roughly similar DFS and OS to the patients with no increase, and a more favourable survival compared to the patients with a persistent increase. In the LIPSYT cohort, the hazard ratio was 0.21 for DFS (CI 0.07-0.66) and 0.24 for OS (CI 0.08-0.76). Transient increases in CA19-9 and YKL-40 tended to be associated with a favourable survival. A transient increase in CEA during adjuvant chemotherapy is associated with a favourable survival when compared with a persistent increase.
血清癌胚抗原(CEA)常用于检测结直肠癌(CRC)手术后的复发。辅助化疗期间 CEA 短暂升高的临床意义尚不清楚。在 LIPSYT 随机研究人群中,在辅助 5-氟尿嘧啶为基础的化疗期间测量了血清 CEA、CA19-9、CRP、YKL-40 和 IL-6。将生物标志物动力学模式分为三组:无增加、短暂增加(≥10%增加后减少)和辅助治疗期间持续增加,并通过使用 Cox 回归分析研究这些模式与无病生存(DFS)和总生存(OS)的关系。这些发现通过接受现代辅助化疗的两个单中心队列得到了验证。在所有队列中,约一半的患者在化疗期间 CEA 出现短暂升高。与无增加的患者相比,CEA 短暂增加的患者 DFS 和 OS 大致相似,与持续增加的患者相比,生存更为有利。在 LIPSYT 队列中,DFS 的风险比为 0.21(CI 0.07-0.66),OS 的风险比为 0.24(CI 0.08-0.76)。CA19-9 和 YKL-40 的短暂增加往往与有利的生存相关。与持续增加相比,辅助化疗期间 CEA 的短暂增加与有利的生存相关。