The association of metabolic disorders and prognosis in cancer patients.

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Tác giả: Zhaoting Bu, Yue Chen, Yi Li, Chenan Liu, Xiaoyue Liu, Hanping Shi, Jinyu Shi, Shuyao Wang, Changhong Xu, Bing Yin, Hong Zhao, Xin Zheng

Ngôn ngữ: eng

Ký hiệu phân loại: 594.38 *Pulmonata

Thông tin xuất bản: England : BMC cancer , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 184410

 OBJECTIVE: Metabolic disorders are common in cancer patients. This study aimed to classify the metabolic disorder status of cancer patients using hematological indicators and to examine the association between disorder types and prognosis. METHODS: A cohort of 6307 patients from INSCOC was classified into three clusters via K-means clustering based on hematological indicators. Logistic regression and Cox models assessed each cluster's impact on adverse outcomes. RESULTS: A total of 6,307 participants were included in the study, K-means clustering divided the population into three groups, Cluster 1 (Normal Group, NG), Cluster 2 (Mild Disorder Group, MDG) and Cluster 3 (Severe Disorder Group, SDG). Compared to NG, MDG (OR = 2.268
  95% CI: 1.967-2.616) and SDG (OR = 4.317
  95% CI: 2.441-7.634) had significantly higher risks of sarcopenia. MDG (OR = 1.943
  95% CI: 1.717-2.198) was associated with a higher risk of moderate malnutrition, and both MDG (OR = 3.786
  95% CI: 3.282-4.368) and SDG (OR = 14.501
  95% CI: 6.847-30.709) were identified as risk factors for severe malnutrition (p <
  0.05). Cox regression analysis indicated that MDG and SDG were independent risk factors for all-cause mortality (MDG: HR = 1.460, 95% CI: 1.341-1.590
  SDG: HR = 2.257, 95% CI: 1.622-3.140) and cancer-specific mortality (MDG: HR = 1.192, 95% CI: 1.039-1.367
  SDG: HR = 2.068, 95% CI: 1.825-2.343) (p <
  0.05). CONCLUSION: K-means clustering effectively categorized metabolic disorder subgroups, supporting targeted interventions and demonstrating a significant link between disorder severity and adverse outcomes.
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