NEW-ONSET AND PRE-EXISTING CARDIOVASCULAR COMORBIDITIES AND SURVIVAL OF LUNG CANCER PATIENTS IN KOREA

IF 5.9 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Kui Son CHOI , Dong-Woo CHOI Ph.D. , Hye Jin YOON MPH
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引用次数: 0

Abstract

Therapeutic Area

ASCVD/CVD in Special Populations

Background

Lung cancer patients exhibit the highest incidence of cardiovascular comorbidities among all cancer types. However, the impact of the timing of cardiovascular disease (CVD) onset on mortality risk in lung cancer patients remains unclear. This study aimed to assess the role of pre-existing and new-onset CVD in survival of patients with non-small cell lung cancer (NSCLC).

Methods

3,144 patients with non-small cell lung cancer (NSCLC) who visited the National Cancer Center in Korea (2012-2017) were analyzed. CVD status was categorized into “none”, “pre-existing”, and “new-onset”, defined by hospitalization for myocardial infarction (I21–I23, MI), ischemic stroke (I63, G45, STR), or heart failure (I50, HF) within 1 year before or after NSCLC diagnosis, using the International Classification of Diseases, 10th Revision (ICD-10). Cox regression analysis using landmark approach (1 year landmark period) and A time-dependent Cox regression analysis were performed to confirm the consistency of the results. Furthermore, the pre-existing group was subdivided into “stable pre-existing” (CVD diagnosed only before cancer) and “recurrent” (CVD events recurring after cancer diagnosis) groups.

Results

Of 3,144 NSCLC patients (mean age 64.2 years; 36.9% women), 92.8% had no CVD, 3.6% had pre-existing CVD, and 3.7% had new-onset CVD. Mortality was highest in the new-onset group (61.7%), followed by pre-existing (54.5%), and none (47.8%). New-onset CVD was associated with increased mortality risk compared to non-CVD group (adjusted Hazard Ratio [aHR]: 1.90, 95% Confidence Interval [CI]: 1.47-2.45), In contrast, the pre-existing or recurrent CVD groups did not show a significant increase in mortality risk. This pattern was consistent across each CVD component analyzed. Moreover, time-dependent Cox regression analysis produced consistent results, thereby supporting the robustness of the findings. Additionally, the highest mortality risk in the new-onset group occurred at 1 year (aHR: 2.29, 95% CI: 1.65-3.18). Subgroup analysis revealed heterogeneity in mortality risks among women, patients with BMI <25 kg/m², and smokers.

Conclusions

Among patients with NSCLC, new-onset CVD was strongly associated with increased mortality, particularly within the first year after diagnosis. These findings highlight the critical importance of early cardiovascular risk detection and proactive management in NSCLC patients, underscoring the need for integrated cardio-oncology approaches.
韩国肺癌患者的新发和既往心血管合并症和生存率
治疗领域ascvd /特殊人群CVD研究背景肺癌患者在所有癌症类型中心血管合并症的发生率最高。然而,心血管疾病(CVD)发病时间对肺癌患者死亡风险的影响尚不清楚。本研究旨在评估已存在和新发CVD在非小细胞肺癌(NSCLC)患者生存中的作用。方法对2012-2017年在韩国国立癌症中心就诊的3144例非小细胞肺癌(NSCLC)患者进行分析。CVD状态分为“无”、“既往存在”和“新发”,定义为在非小细胞肺癌诊断前后1年内因心肌梗死(I21-I23, MI)、缺血性卒中(I63, G45, STR)或心力衰竭(I50, HF)住院。采用里程碑法(1年里程碑期)进行Cox回归分析,并进行时间相关Cox回归分析,以确认结果的一致性。此外,既存组被细分为“稳定既存”组(仅在癌症前诊断出心血管疾病)和“复发”组(心血管疾病事件在癌症诊断后复发)。结果在3144例非小细胞肺癌患者(平均年龄64.2岁,36.9%为女性)中,92.8%无CVD, 3.6%既往存在CVD, 3.7%为新发CVD。死亡率最高的是新发组(61.7%),其次是既往病史组(54.5%)和无病史组(47.8%)。与非CVD组相比,新发CVD与死亡风险增加相关(调整后的危险比[aHR]: 1.90, 95%可信区间[CI]: 1.47-2.45),相比而言,已存在或复发CVD组的死亡风险没有显著增加。这种模式在分析的每个CVD成分中都是一致的。此外,时间相关的Cox回归分析产生了一致的结果,从而支持了研究结果的稳健性。此外,新发组的最高死亡风险发生在1年(aHR: 2.29, 95% CI: 1.65-3.18)。亚组分析显示,女性、BMI≤25kg /m²的患者和吸烟者之间的死亡风险存在异质性。结论:在非小细胞肺癌患者中,新发心血管疾病与死亡率增加密切相关,特别是在诊断后的第一年。这些发现强调了早期心血管风险检测和主动管理对非小细胞肺癌患者的重要性,强调了综合心血管肿瘤学方法的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American journal of preventive cardiology
American journal of preventive cardiology Cardiology and Cardiovascular Medicine
CiteScore
6.60
自引率
0.00%
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0
审稿时长
76 days
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