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Predictors for development of palbociclib-induced neutropenia in breast cancer patients as determined by ordered logistic regression analysis
Predictors for development of palbociclib-induced neutropenia in breast cancer patients as determined by ordered logistic regression analysis
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Predictors for development of palbociclib-induced neutropenia in breast cancer patients as determined by ordered logistic regression analysis
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Predictors for development of palbociclib-induced neutropenia in breast cancer patients as determined by ordered logistic regression analysis
Predictors for development of palbociclib-induced neutropenia in breast cancer patients as determined by ordered logistic regression analysis

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Predictors for development of palbociclib-induced neutropenia in breast cancer patients as determined by ordered logistic regression analysis
Predictors for development of palbociclib-induced neutropenia in breast cancer patients as determined by ordered logistic regression analysis
Journal Article

Predictors for development of palbociclib-induced neutropenia in breast cancer patients as determined by ordered logistic regression analysis

2021
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Overview
This retrospective study aimed to identify predictors for the development of palbociclib-induced neutropenia. This study retrospectively analysed 78 breast cancer patients who had received palbociclib at our hospital between January 2018 and May 2020. For the regression analysis of factors associated with palbociclib-induced neutropenia, variables were extracted manually from medical charts. The level of palbociclib-induced neutropenia was evaluated using the National Cancer Institute’s Common Terminology Criteria for Adverse Events (version 5). Multivariate ordered logistic regression analysis was performed to identify predictors for the development of neutropenia. Optimal cut-off thresholds were determined using receiver operating characteristic (ROC) analysis. Values of P  < 0.05 (2-tailed) were considered significant. Significant factors identified included concomitant use of statin (odds ratio [OR] = 0.104, 95% confidence interval [CI] = 0.018–0.598; P  = 0.011) and body mass index (BMI) (OR = 1.118, 95% CI = 1.007–1.241; P  = 0.037). ROC analysis revealed that neutropenia (grade 4) was more likely to occur with a BMI ≥ 22.3 kg/m 2 . In conclusion, no concomitant use of statins and high BMI were identified as significant predictors for the development of palbociclib-induced neutropenia.