Predictive accuracy of phase angle for short-term and stage-specific mortality in cancer.
2/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
환자: cancer in Brazil (≥18 y; 51
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSION] PhA is an independent predictor of short-term mortality in cancer across all TNM stages. Identified thresholds (consistently < 5.5°) may guide risk stratification and support clinical decision-making, although external validation is required.
OpenAlex 토픽 ·
Body Composition Measurement Techniques
Electrical and Bioimpedance Tomography
Electromagnetic Fields and Biological Effects
[BACKGROUND AND AIMS] Cancer-related factors can negatively affect nutritional status and impact disease trajectory.
APA
Amanda S. Rebouças, Jarson P Costa-Pereira, et al. (2026). Predictive accuracy of phase angle for short-term and stage-specific mortality in cancer.. Nutrition (Burbank, Los Angeles County, Calif.), 147, 113170. https://doi.org/10.1016/j.nut.2026.113170
MLA
Amanda S. Rebouças, et al.. "Predictive accuracy of phase angle for short-term and stage-specific mortality in cancer.." Nutrition (Burbank, Los Angeles County, Calif.), vol. 147, 2026, pp. 113170.
PMID
41930790 ↗
Abstract 한글 요약
[BACKGROUND AND AIMS] Cancer-related factors can negatively affect nutritional status and impact disease trajectory. Prognostic biomarkers such as bioelectrical impedance-derived phase angle (PhA) may help identify patients at higher risk of adverse outcomes. This study aimed to determine optimal PhA cut-off points associated with short-term mortality across different cancer stages.
[METHODS] This multicenter cohort included 1121 adult patients with cancer in Brazil (≥18 y; 51.2% females; mean age 60 ± 13 y; 43.6% colorectal cancer; 34.3% tumor, node, metastasis [TNM] IV). PhA was derived from raw bioelectrical impedance values: resistance (R) and reactance (Xc) from a tetrapolar single-frequency device (50 kHz). The primary outcome was 6-mo mortality. PhA's predictive accuracy was estimated using receiver operating characteristic (ROC) curves, and cut-off points were estimated using the Youden index. Cox regression models examined crude and adjusted associations between PhA and mortality across TNM stages (I-IV).
[RESULTS] PhA values were significantly lower in non-survivors (mean difference: -1.02° in males; -1.21° in females). ROC analyses demonstrated fair predictive performance, with optimal thresholds of ≤ 5.43° for males (AUROC 0.74) and ≤ 4.22° for females (AUROC 0.77). Across TNM stages, PhA consistently predicted mortality, with highest accuracy in stage IV (AUROC 0.75; criterion ≤ 4.72°). In multivariate Cox models, PhA remained independently associated with 6-mo mortality after adjustment for confounders. Stepwise analyses confirmed these findings across all stages.
[CONCLUSION] PhA is an independent predictor of short-term mortality in cancer across all TNM stages. Identified thresholds (consistently < 5.5°) may guide risk stratification and support clinical decision-making, although external validation is required.
[METHODS] This multicenter cohort included 1121 adult patients with cancer in Brazil (≥18 y; 51.2% females; mean age 60 ± 13 y; 43.6% colorectal cancer; 34.3% tumor, node, metastasis [TNM] IV). PhA was derived from raw bioelectrical impedance values: resistance (R) and reactance (Xc) from a tetrapolar single-frequency device (50 kHz). The primary outcome was 6-mo mortality. PhA's predictive accuracy was estimated using receiver operating characteristic (ROC) curves, and cut-off points were estimated using the Youden index. Cox regression models examined crude and adjusted associations between PhA and mortality across TNM stages (I-IV).
[RESULTS] PhA values were significantly lower in non-survivors (mean difference: -1.02° in males; -1.21° in females). ROC analyses demonstrated fair predictive performance, with optimal thresholds of ≤ 5.43° for males (AUROC 0.74) and ≤ 4.22° for females (AUROC 0.77). Across TNM stages, PhA consistently predicted mortality, with highest accuracy in stage IV (AUROC 0.75; criterion ≤ 4.72°). In multivariate Cox models, PhA remained independently associated with 6-mo mortality after adjustment for confounders. Stepwise analyses confirmed these findings across all stages.
[CONCLUSION] PhA is an independent predictor of short-term mortality in cancer across all TNM stages. Identified thresholds (consistently < 5.5°) may guide risk stratification and support clinical decision-making, although external validation is required.
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