AI Article Synopsis

  • - The study examined the effectiveness of inflammation-based prognostic scores in predicting outcomes for patients with locally advanced cervical esophageal squamous cell carcinoma (ESCC) undergoing curative concurrent chemoradiotherapy (CCRT).
  • - A total of 411 ESCC patients were included, with significant findings that specific scores like Neutrophil Lymphocyte Ratio (NLR) and Modified Glasgow Prognostic Score (mGPS) were linked to worse overall survival rates.
  • - The results highlighted that PLR and mGPS could serve as independent prognostic indicators, proving relevant not only for cervical ESCC but also showing compatibility with findings in thoracic ESCC patients.

Article Abstract

Introduction: The present study investigated the crucial role of inflammation-based prognostic scores in locally advanced cervical esophageal squamous cell carcinoma (ESCC) patients who underwent curative concurrent chemoradiotherapy (CCRT).

Methods: There were 411 ESCC patients enrolled, including 63 cervical ESCC patients. Using the propensity score matching method, 63 thoracic ESCC patients were matched to the 63 cervical ESCC patients. The inflammation-based prognostic scores included the neutrophil lymphocyte ratio (NLR), platelet lymphocyte ratio (PLR), albumin level, c-reactive protein (CRP) level, modified Glasgow prognostic score (mGPS), and CRP/albumin ratio. The chi-square test and Kaplan-Meier method were used for categorical variable data and overall survival, respectively. A Cox regression model was performed for univariate and multivariable analyses.

Results: With respect to cervical ESCC, NLR ≥ 2.5 ( = 0.019), PLR ≥ 103 ( = 0.013), CRP value >10 mg/l ( = 0.040), mGPS ≥ 1 ( = 0.040), and CRP/albumin ratio ≥ 9.5 ( = 0.033) were significant predictors of worse overall survival (OS) in the univariate analysis. In a multivariable analysis, PLR ≥ 103 ( = 0.010, HR: 2.66, 95% CI [1.27-5.58]) and mGPS ≥ 1 ( = 0.030, HR: 2.03, 95% CI [1.07-3.86]) were the independent prognostic parameters of worse OS. The prognostic value of these biomarkers in the matched thoracic ESCC patients was similar and compatible with the results in the cervical ESCC group in the univariate and multivariable analyses.

Conclusions: Our study suggests that these inflammation-based prognostic scores are helpful in clinical practice, and PLR and mGPS may predict the prognosis for locally advanced cervical ESCC patients who receive curative CCRT.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151110PMC
http://dx.doi.org/10.7717/peerj.5655DOI Listing

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