Correlation between sarcopenia diagnosed by C3SMI criteria and prognosis in esophageal cancer patients after radiotherapy.

IF 2.5 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
De-En Wang, Xiao-Fang Qin, Wei Yang
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引用次数: 0

Abstract

Background: Esophageal cancer is a common malignancy with high mortality. Radiotherapy is an important treatment. Sarcopenia affects patients' physical function and prognosis. However, the relationship between sarcopenia diagnosed by Chun-Hou Chen method for sarcopenia measurement and index (C3SMI) criteria and esophageal cancer prognosis after radiotherapy is unclear.

Aim: To explore the correlation between sarcopenia (SA) diagnosed based on C3SMI criteria and the prognosis of patients with esophageal cancer following radiotherapy.

Methods: A retrospective analysis was conducted on the general clinical data of 131 esophageal cancer patients who received radiotherapy in the Affiliated Huaian No. 1 People's Hospital of Nanjing Medical University from March 2021 to July 2024. Based on the presence of SA, the patients were assigned into two groups - the SA group and the non-SA group. Logistic regression analysis was used for investigating the risk factors influencing SA in esophageal cancer patients. Additionally, the patients were followed up, with their prognosis recorded. As per their prognostic outcomes, the patients were allocated into a good prognosis group and a poor prognosis group. The data of the two groups were compared. Using logistic regression analysis, the risk factors that may influence the prognosis of these patients were analyzed. SPSS 26.0 statistical software was introduced for analyzing the study data. Comparisons were made between groups using t-tests or χ 2 tests based on the data type.

Results: As revealed through logistic regression analysis, age [odds ratio (OR) = 2.898, P = 0.038], body mass index (OR = 5.983, P = 0.006), prealbumin (OR = 6.253, P = 0.003), and Karnofsky performance status score (OR = 3.854, P = 0.010) were independent risk factors impacting SA for esophageal cancer patients (P < 0.05). Logistic regression analysis also found that age (OR = 3.823, P = 0.030), differentiation degree (OR = 4.802, P = 0.028), American Joint Committee on Cancer clinical staging (OR = 3.732, P = 0.013), alpha-fetoprotein level (OR = 3.508, P = 0.018), thrombospondin-1 level (OR = 5.749, P = 0.006), carcinoembryonic antigen level (OR = 3.873, P = 0.030), and SA (OR = 3.593, P = 0.017) were independent risk factors that may influence esophageal cancer patients' prognosis (P < 0.05).

Conclusion: The presence of SA has a significant relation to the poor prognosis of esophageal cancer patients, which highlights the importance of assessing and intervening in SA in clinical management so as to improve patient prognosis.

Abstract Image

食管癌放疗后C3SMI诊断肌少症与预后的关系
背景:食管癌是一种常见的恶性肿瘤,死亡率高。放射治疗是一种重要的治疗方法。肌肉减少症影响患者的身体机能和预后。然而,采用陈淳厚法测定骨骼肌减少指数(C3SMI)标准诊断的骨骼肌减少症与食管癌放疗后预后的关系尚不清楚。目的:探讨基于C3SMI标准诊断的肌少症(sarcopenia, SA)与食管癌放疗后预后的相关性。方法:回顾性分析南京医科大学附属淮安第一人民医院2021年3月至2024年7月131例食管癌放疗患者的一般临床资料。根据SA的存在,将患者分为SA组和非SA组。采用Logistic回归分析探讨影响食管癌患者SA发生的危险因素。并对患者进行随访,记录预后。根据预后情况将患者分为预后好组和预后差组。比较两组数据。采用logistic回归分析,分析可能影响患者预后的危险因素。采用SPSS 26.0统计软件对研究数据进行分析。根据数据类型使用t检验或χ 2检验进行组间比较。结果:logistic回归分析显示,年龄[优势比(OR) = 2.898, P = 0.038]、体重指数(OR = 5.983, P = 0.006)、前白蛋白(OR = 6.253, P = 0.003)、Karnofsky性能状态评分(OR = 3.854, P = 0.010)是影响食管癌患者SA的独立危险因素(P < 0.05)。逻辑回归分析还发现,年龄(或= 3.823,P = 0.030),分化程度(或= 4.802,P = 0.028),美国癌症联合委员会临床分期(或= 3.732,P = 0.013),甲胎蛋白水平(或= 3.508,P = 0.018),血小板反应蛋白- 1的水平(或= 5.749,P = 0.006),癌胚抗原水平(或= 3.873,P = 0.030),和SA(或= 3.593,P = 0.017)的独立危险因素,可能会影响食管癌患者的预后(P < 0.05)。结论:SA的存在与食管癌患者预后不良有显著关系,因此在临床管理中对SA进行评估和干预,以改善患者预后具有重要意义。
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来源期刊
World Journal of Gastrointestinal Oncology
World Journal of Gastrointestinal Oncology Medicine-Gastroenterology
CiteScore
4.20
自引率
3.30%
发文量
1082
期刊介绍: The World Journal of Gastrointestinal Oncology (WJGO) is a leading academic journal devoted to reporting the latest, cutting-edge research progress and findings of basic research and clinical practice in the field of gastrointestinal oncology.
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