血清胆碱酯酶的纵向评价有利于常见类型人类癌症的预后监测。

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Chunxia Li, Yanli Li, Lizhu Liu, Ruimin You, Bingbing Fan, Jiali Lv, Dingyun You, Zhenhui Li, Tao Zhang
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引用次数: 0

摘要

背景:关于血清胆碱酯酶(ChE)对癌症预后影响的现有文献主要是评估术前水平,而忽略了术后随访期间的一系列ChE测量。方法:回顾性分析5925例I-III期非小细胞肺癌(NSCLC)、结直肠癌(CRC)和胃癌(GC)行根治性手术的患者。将患者分为持续正常、归一化、降低和持续低围手术期ChE模式,以及通过潜在类别生长混合模型(LCGMM)识别的纵向ChE轨迹。评估ChE动态变化与总生存期(OS)和无复发生存期(RFS)的关系。结果:考虑术前水平后,术后ChE成为一个独立的预后因素。围手术期ChE分层显示不同的生存结果:持续正常组(82.5%)的5年OS比降低组(73.9%)高8.6%,而正常化组(73.3%)的5年OS比持续低组(59.4%)高13.9%。LCGMM确定了三种不同的纵向轨迹:缓慢上升(5年OS率:79.7%,参照组),上升-下降(5年OS率:64.8%,调整HR: 1.50, 95% CI: 1.14至1.99)和下降-上升(5年OS率:58.1%,调整HR: 2.33, 95% CI: 1.69至3.22)。RFS也观察到一致的结果。此外,分层分析证实了所有组织学亚型中ChE动态变化与预后的统计学显著相关性。结论:建议术后常规随访测量ChE,以改善癌症患者的个体化管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Longitudinal evaluation of serum cholinesterase benefits prognosis surveillance of common types of human cancer.

Background: Existing literature on serum cholinesterase (ChE) in cancer prognosis have predominantly evaluated preoperative levels, ignoring serial ChE measurements during postoperative follow-up.

Methods: 5925 patients undergoing curative resection for stage I-III non-small cell lung cancer (NSCLC), colorectal cancer (CRC), and gastric cancer (GC) were retrospectively included. Patients were divided into persistently normal, normalized, lowered and persistently low perioperative ChE patterns, as well as longitudinal ChE trajectories identified by the latent class growth mixed model (LCGMM). The associations of ChE dynamic changes with overall survival (OS) and recurrence-free survival (RFS) were evaluated.

Results: Postoperative ChE emerged as an independent prognostic factor, event after accounting for preoperative levels. Perioperative ChE stratification revealed divergent survival outcomes: the persistently normal group (82.5%) demonstrated 8.6% higher 5-year OS rate than the lowered group (73.9%), while the normalized group (73.3%) had 13.9% higher 5-year OS rate than the persistently low group (59.4%). LCGMM identified three distinct longitudinal trajectories: slow-rising (5-year OS rate: 79.7%; reference group), rising-decreasing (5-year OS rate: 64.8%; adjusted HR: 1.50, 95% CI: 1.14 to 1.99) and decreasing-rising (5-year OS rate: 58.1%; adjusted HR: 2.33, 95% CI: 1.69 to 3.22). Consistent results were observed for RFS as well. Furthermore, stratified analyses confirmed statistically significant associations of ChE dynamic changes with prognosis across all histological subtypes.

Conclusions: A routine follow-up measurement of postoperative ChE was recommended to improve individualized management of cancer patients.

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