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氨基转移酶与淋巴细胞比值作为I-III期结直肠癌患者的一种有价值的预后标志物:一项回顾性研究

Aminotransferase-to-lymphocyte ratio as a valuable prognostic marker for patients with stage I-III colorectal cancer: a retrospective study.

作者信息

Xie Hailun, Wei Lishuang, Tang Shuangyi, Gan Jialiang

机构信息

Department of Gastrointestinal and Gland Surgery, The First Affiliated Hospital, Guangxi Medical University, Nanning, China.

Guangxi Key Laboratory of Enhanced Recovery after Surgery for Gastrointestinal Cancer, The First Affiliated Hospital, Guangxi Medical University, Nanning, China.

出版信息

Front Oncol. 2024 Nov 18;14:1446557. doi: 10.3389/fonc.2024.1446557. eCollection 2024.

DOI:10.3389/fonc.2024.1446557
PMID:39624626
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11609077/
Abstract

BACKGROUND

There are no population-based studies on the prognostic value of the preoperative aminotransferase-to-lymphocyte ratio (AALR) in predicting recurrence and survival in patients with colorectal cancer (CRC) who have undergone curative resection.

AIM

This study explored the relationship between AALR and prognosis of CRC patients, specifically stage III CRC.

METHODS

Restricted Cubic Splines were used to evaluate the relationship between AALR and outcomes. The survival curve was generated using the Kaplan-Meier method and the log-rank test. COX regression analysis was used to identify the independent prognostic factors of CRC patients. Logistic regression analysis was used to assess the independent risk factors affecting sarcopenia and postoperative complications. Concordance index and calibration curves were used to evaluate the discriminative ability of the prognostic nomograms. Finally, according to a ratio of 7:3, the total population was randomized into two cohorts to validate the practicability of the prognostic nomograms.

RESULTS

In total, 1304 stage I-III CRC were enrolled in this study. There was a significant positive correlation between AALR and PFS/OS in CRC patients. The PFS/OS ratio of the high AALR group was significantly lower than that of the low AALR group. In the subgroup analysis, we found that the AALR significantly stratified the prognosis of patients with stage III CRC. A high AALR was still independently associated with poor PFS (HR = 1.335, 95% CI =1.075-1.657, p=0.009) and OS (HR = 1.382, 95% CI =1.139-1.677, p=0.001) in CRC patients. Variables with a value ≤ 0.05 in multivariable analysis were incorporated into the construction of prognostic nomograms for predicting 1-5 years PFS/OS of CRC patients. The results of the concordance index and calibration curves confirmed that these prognostic nomograms had a good prediction accuracy. In addition, we demonstrated the good predictive performance of these nomograms in a randomized internal validation cohort.

CONCLUSION

AALR is an effective prognostic marker for predicting long-term outcomes and could provide a valuable reference for sarcopenia and postoperative complications in CRC patients. AALR-based nomograms have good predictive accuracy and can help to develop individualized risk stratification, follow-up, and treatment strategies for CRC patients.

摘要

背景

目前尚无基于人群的研究探讨术前转氨酶与淋巴细胞比值(AALR)对接受根治性切除的结直肠癌(CRC)患者复发和生存的预后价值。

目的

本研究探讨AALR与CRC患者,特别是III期CRC患者预后的关系。

方法

采用限制性立方样条评估AALR与预后的关系。使用Kaplan-Meier法和对数秩检验生成生存曲线。采用COX回归分析确定CRC患者的独立预后因素。采用逻辑回归分析评估影响肌肉减少症和术后并发症的独立危险因素。使用一致性指数和校准曲线评估预后列线图的判别能力。最后,按照7:3的比例将总人群随机分为两个队列,以验证预后列线图的实用性。

结果

本研究共纳入1304例I-III期CRC患者。CRC患者的AALR与无进展生存期(PFS)/总生存期(OS)之间存在显著正相关。高AALR组的PFS/OS比值显著低于低AALR组。在亚组分析中,我们发现AALR显著分层了III期CRC患者的预后。高AALR仍然与CRC患者较差的PFS(风险比[HR]=1.335,95%置信区间[CI]=1.075-1.657,p=0.009)和OS(HR = 1.382,95% CI =1.139-1.677,p=0.001)独立相关。多变量分析中P值≤0.05的变量被纳入构建用于预测CRC患者1-5年PFS/OS的预后列线图。一致性指数和校准曲线的结果证实这些预后列线图具有良好的预测准确性。此外,我们在随机内部验证队列中证明了这些列线图具有良好的预测性能。

结论

AALR是预测长期预后的有效预后标志物,可为CRC患者的肌肉减少症和术后并发症提供有价值的参考。基于AALR的列线图具有良好的预测准确性,有助于为CRC患者制定个体化的风险分层、随访和治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2b3/11609077/10b92bb31b7d/fonc-14-1446557-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2b3/11609077/8e7d2f97087a/fonc-14-1446557-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2b3/11609077/cd9ab2cda6ec/fonc-14-1446557-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2b3/11609077/10b92bb31b7d/fonc-14-1446557-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2b3/11609077/8e7d2f97087a/fonc-14-1446557-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2b3/11609077/cd9ab2cda6ec/fonc-14-1446557-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2b3/11609077/10b92bb31b7d/fonc-14-1446557-g003.jpg

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