Determining the cut-off value of the MASCC Score to predict mortality in hospitalized febrile neutropenic patients: A decade-long single-center retrospective cohort study

医学 内科学 比例危险模型 癌症 发热性中性粒细胞减少症 恶性肿瘤 混淆 队列 中性粒细胞减少症 多元分析 回顾性队列研究 死亡率 血液恶性肿瘤 化疗
作者
Yasemin Nadir,Pınar Kıran,Damla Ertürk,Hoşeng Bülbül,Mustafa Değirmenci,Süheyla Serin Senger
出处
期刊:Oncology [Karger Publishers]
卷期号:: 1-13
标识
DOI:10.1159/000546029
摘要

Introduction: Febrile neutropenia [FN] is linked to significant morbidity and mortality in cancer patients. Therefore, our study aims to determine the cut-off value of the MASCC Score to predict mortality in hospitalized FN patients. Methods: We included 354 hospitalized cancer patients, divided into two groups: the mortality group [n=116] and the survival group [n=238]. We defined risk factors of all-cause mortality according to Cox regression model. The optimal cut-off value for MASCC score was found using Youden's index. Results: The 30-day, 60-day, and 90-day mortality rates were 25.1% [n=89], 30.2% [n=107], and 32.7% [n=116], respectively. Having a hematological malignancy, advence age, comorbidities, higher levels of C-reactive protein and procalctonin on admission, profound neutropenia and a lower MASCC score were statistically different in the mortality group compared to the survival group. The only independent risk factor was the MASCC score to predict all-cause mortality according to the multivariate Cox regression models. A MASCC score below 17 showed a sensitivity of 83.6% and a specificity of 94.1% for predicting all-cause mortality in hospitalized FN patients. Conclusions: In this cohort study, we showed 30,60 and 90-day mortality rates of hospitalized patients and determined the risk factors. We supported that the MASCC score was an independent risk factor for predicting mortality in hospitalized FN patients. We contributed to the literature by establishing a threshold value for the MASCC score, below 17, showing notably high sensitivity and specificity for predicting all-cause mortality in FN patients.

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