論文

国際誌
2022年6月18日

Prognostic value of systemic inflammatory markers and the nutrition status in thymic epithelial tumors with complete resection.

Thoracic cancer
  • Tadashi Sakane
  • ,
  • Katsuhiro Okuda
  • ,
  • Takuya Matsui
  • ,
  • Risa Oda
  • ,
  • Tsutomu Tatematsu
  • ,
  • Keisuke Yokota
  • ,
  • Ryoichi Nakanishi

13
15
開始ページ
2127
終了ページ
2133
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1111/1759-7714.14485

BACKGROUND: Recent studies have shown that several systemic inflammatory markers and the nutrition status, including the neutrophil-to-lymphocyte ratio (NLR), monocyte-to-lymphocyte ratio (MLR), platelet-to-lymphocyte ratio (PLR), and prognostic nutritional index (PNI), are useful prognostic factors in several malignant tumors. The present study explored the prognostic value of the NLR, MLR, PLR, and PNI in thymic epithelial tumor (TET) patients who underwent complete resection. METHODS: A total of 158 TET patients who underwent complete resection were involved in the analysis. Their NLR, MLR, PLR, and PNI values were obtained from a blood examination within one month before the initiation of treatment. A receiver operating characteristic curve analysis was conducted to determine the optimal cutoff values. RESULTS: The enrolled patients were stratified by cutoffs of 4.35 for the NLR, 0.22 for the MLR, 130.18 for the PLR, and 44.02 for the PNI. A univariate analysis revealed that high-grade malignant TET, including type B2 and B3 thymoma, thymic carcinoma, and thymic neuroendocrine tumor; an advanced Masaoka stage; a high NLR; a high MLR; and a low PNI were significant predictors of a poor disease-free survival (DFS). A multivariate analysis confirmed that an advanced Masaoka stage (HR = 5.5557, p = 0.0007) and a high MLR (HR = 3.3371, p = 0.0264) were independent predictors of a poor DFS. CONCLUSIONS: Our study demonstrated that the pretreatment MLR was an independent predictor of the DFS in patients with TETs who underwent complete resection.

リンク情報
DOI
https://doi.org/10.1111/1759-7714.14485
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/35715991
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346175
ID情報
  • DOI : 10.1111/1759-7714.14485
  • PubMed ID : 35715991
  • PubMed Central 記事ID : PMC9346175

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