{"title":"美国转移性结直肠癌患者血清乳酸脱氢酶的真实世界检测。","authors":"Heinz-Josef Lenz, Orsolya Lunacsek, Helene Ostojic, Xiaoyun Pan, Emmanuelle Dochy, Zdravko Vassilev, Nasreen Khan","doi":"10.1093/oncolo/oyaf192","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Serum lactate dehydrogenase (LDH) is a potential prognostic biomarker of outcomes in patients with metastatic colorectal cancer (mCRC). This retrospective, observational study assessed real-world LDH testing patterns and LDH as a prognostic factor for overall survival (OS) in US patients receiving chemotherapy for mCRC.Patients and methods: Patients with mCRC who initiated first-line chemotherapy between January 1, 2016, and November 30, 2022, were selected from a nationwide de-identified Electronic Health Record-derived database. LDH value was categorized based on laboratory reference ranges. The prognostic relationship between pretreatment LDH value and OS was assessed using Kaplan-Meier and multivariate Cox proportional-hazards models.</p><p><strong>Results: </strong>Of 15 329 adult patients (median age 64 years), 3379 (22%) had LDH testing at or post-index; 21% had abnormal baseline values, while 40% had normal values. Patients with abnormal LDH levels were more likely to be female (47% abnormal LDH vs 41% normal LDH), age ≥65 years (52% vs 49%), African American or Black (12% vs 7%), or reside in the Northeast (30% vs 21%). The median OS (95% CI) in patients with normal baseline LDH was 29.9 (28.3-31.7) vs 16.8 (14.8-18.2) months for those with abnormal LDH. In a multivariate Cox proportional-hazards model, patients with abnormal baseline LDH had higher risk of death (HR 1.91, P < .0001) after adjustment for demographic/clinical characteristics.</p><p><strong>Conclusion: </strong>Abnormal baseline LDH levels were associated with shorter OS; however, only one-fifth of patients receiving chemotherapy underwent LDH testing. Efforts to increase LDH testing could be valuable in helping guide treatment decisions.</p>","PeriodicalId":54686,"journal":{"name":"Oncologist","volume":" ","pages":""},"PeriodicalIF":4.8000,"publicationDate":"2025-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Real-world testing of serum lactate dehydrogenase among patients with metastatic colorectal cancer in the USA.\",\"authors\":\"Heinz-Josef Lenz, Orsolya Lunacsek, Helene Ostojic, Xiaoyun Pan, Emmanuelle Dochy, Zdravko Vassilev, Nasreen Khan\",\"doi\":\"10.1093/oncolo/oyaf192\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Serum lactate dehydrogenase (LDH) is a potential prognostic biomarker of outcomes in patients with metastatic colorectal cancer (mCRC). This retrospective, observational study assessed real-world LDH testing patterns and LDH as a prognostic factor for overall survival (OS) in US patients receiving chemotherapy for mCRC.Patients and methods: Patients with mCRC who initiated first-line chemotherapy between January 1, 2016, and November 30, 2022, were selected from a nationwide de-identified Electronic Health Record-derived database. LDH value was categorized based on laboratory reference ranges. The prognostic relationship between pretreatment LDH value and OS was assessed using Kaplan-Meier and multivariate Cox proportional-hazards models.</p><p><strong>Results: </strong>Of 15 329 adult patients (median age 64 years), 3379 (22%) had LDH testing at or post-index; 21% had abnormal baseline values, while 40% had normal values. Patients with abnormal LDH levels were more likely to be female (47% abnormal LDH vs 41% normal LDH), age ≥65 years (52% vs 49%), African American or Black (12% vs 7%), or reside in the Northeast (30% vs 21%). The median OS (95% CI) in patients with normal baseline LDH was 29.9 (28.3-31.7) vs 16.8 (14.8-18.2) months for those with abnormal LDH. In a multivariate Cox proportional-hazards model, patients with abnormal baseline LDH had higher risk of death (HR 1.91, P < .0001) after adjustment for demographic/clinical characteristics.</p><p><strong>Conclusion: </strong>Abnormal baseline LDH levels were associated with shorter OS; however, only one-fifth of patients receiving chemotherapy underwent LDH testing. Efforts to increase LDH testing could be valuable in helping guide treatment decisions.</p>\",\"PeriodicalId\":54686,\"journal\":{\"name\":\"Oncologist\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2025-06-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Oncologist\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/oncolo/oyaf192\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oncologist","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/oncolo/oyaf192","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景:血清乳酸脱氢酶(LDH)是转移性结直肠癌(mCRC)患者预后的潜在生物标志物。这项回顾性观察性研究评估了现实世界LDH检测模式和LDH作为美国mCRC化疗患者总生存期(OS)的预后因素。患者和方法:2016年1月1日至2022年11月30日期间开始一线化疗的mCRC患者从全国范围内的电子健康记录衍生数据库中选择。LDH值根据实验室参考范围进行分类。采用Kaplan-Meier和多变量Cox比例风险模型评估预处理LDH值与OS的预后关系。结果:在15329例成人患者(中位年龄64岁)中,3379例(22%)在检查时或检查后进行了LDH检测;21%的患者基线值异常,40%的患者基线值正常。LDH水平异常的患者更可能是女性(47% LDH异常对41%正常LDH),年龄≥65岁(52%对49%),非洲裔美国人或黑人(12%对7%),或居住在东北部(30%对21%)。基线LDH正常患者的中位OS (95% CI)为29.9(28.3-31.7)个月,LDH异常患者的中位OS (95% CI)为16.8(14.8-18.2)个月。在多变量Cox比例风险模型中,调整人口统计学/临床特征后,基线LDH异常的患者死亡风险更高(HR 1.91, P < 0.0001)。结论:基线LDH水平异常与较短的OS相关;然而,只有五分之一接受化疗的患者进行了LDH检测。努力增加LDH检测在帮助指导治疗决策方面可能是有价值的。
Real-world testing of serum lactate dehydrogenase among patients with metastatic colorectal cancer in the USA.
Background: Serum lactate dehydrogenase (LDH) is a potential prognostic biomarker of outcomes in patients with metastatic colorectal cancer (mCRC). This retrospective, observational study assessed real-world LDH testing patterns and LDH as a prognostic factor for overall survival (OS) in US patients receiving chemotherapy for mCRC.Patients and methods: Patients with mCRC who initiated first-line chemotherapy between January 1, 2016, and November 30, 2022, were selected from a nationwide de-identified Electronic Health Record-derived database. LDH value was categorized based on laboratory reference ranges. The prognostic relationship between pretreatment LDH value and OS was assessed using Kaplan-Meier and multivariate Cox proportional-hazards models.
Results: Of 15 329 adult patients (median age 64 years), 3379 (22%) had LDH testing at or post-index; 21% had abnormal baseline values, while 40% had normal values. Patients with abnormal LDH levels were more likely to be female (47% abnormal LDH vs 41% normal LDH), age ≥65 years (52% vs 49%), African American or Black (12% vs 7%), or reside in the Northeast (30% vs 21%). The median OS (95% CI) in patients with normal baseline LDH was 29.9 (28.3-31.7) vs 16.8 (14.8-18.2) months for those with abnormal LDH. In a multivariate Cox proportional-hazards model, patients with abnormal baseline LDH had higher risk of death (HR 1.91, P < .0001) after adjustment for demographic/clinical characteristics.
Conclusion: Abnormal baseline LDH levels were associated with shorter OS; however, only one-fifth of patients receiving chemotherapy underwent LDH testing. Efforts to increase LDH testing could be valuable in helping guide treatment decisions.
期刊介绍:
The Oncologist® is dedicated to translating the latest research developments into the best multidimensional care for cancer patients. Thus, The Oncologist is committed to helping physicians excel in this ever-expanding environment through the publication of timely reviews, original studies, and commentaries on important developments. We believe that the practice of oncology requires both an understanding of a range of disciplines encompassing basic science related to cancer, translational research, and clinical practice, but also the socioeconomic and psychosocial factors that determine access to care and quality of life and function following cancer treatment.