TY - JOUR
T1 - Predicting risk of chemotherapy-induced severe neutropenia
T2 - A pooled analysis in individual patients data with advanced lung cancer
AU - Cao, Xiaowen
AU - Ganti, Apar Kishor
AU - Stinchcombe, Thomas
AU - Wong, Melisa L.
AU - Ho, James C.
AU - Shen, Chen
AU - Liu, Yingzhou
AU - Crawford, Jeffery
AU - Pang, Herbert
AU - Wang, Xiaofei
N1 - Funding Information:
This study was supported in part by the R21-AG042894 from the NIH National Institute on Aging, grant P01-CA142538 from the NIH National Cancer Institute, and Health and Medical Research Fund15162491 of Hong Kong. Dr. Wong was supported by grant KL2-TR001870 from the National Center for Advancing Translational Sciences.
Funding Information:
This study was supported in part by the R21-AG042894 from the NIH National Institute on Aging , grant P01-CA142538 from the NIH National Cancer Institute , and Health and Medical Research Fund 15162491 of Hong Kong. Dr. Wong was supported by grant KL2-TR001870 from the National Center for Advancing Translational Sciences .
Publisher Copyright:
© 2020
PY - 2020/3
Y1 - 2020/3
N2 - Objectives: Neutropenia is associated with the risk of life-threatening infections, chemotherapy dose reductions and delays that may compromise outcomes. This analysis was conducted to develop a prediction model for chemotherapy-induced severe neutropenia in lung cancer. Materials and Methods: Individual patient data from existing cooperative group phase II/III trials of stages III/IV non-small cell lung cancer or extensive small-cell lung cancer were included. The data were split into training and testing sets. In order to enhance the prediction accuracy and the reliability of the prediction model, lasso method was used for both variable selection and regularization on the training set. The selected variables was fit to a logistic model to obtain regression coefficients. The performance of the final prediction model was evaluated by the area under the ROC curve in both training and testing sets. Results: The dataset was randomly separated into training [7606 (67 %) patients] and testing [3746 (33 %) patients] sets. The final model included: age (>65 years), gender (male), weight (kg), BMI, insurance status (yes/unknown), stage (IIIB/IV/ESSCLC), number of metastatic sites (1, 2 or ≥3), individual drugs (gemcitabine, taxanes), number of chemotherapy agents (2 or ≥3), planned use of growth factors, associated radiation therapy, previous therapy (chemotherapy, radiation, surgery), duration of planned treatment, pleural effusion (yes/unknown), performance status (1, ≥2) and presence of symptoms (yes/unknown). Conclusions: We have developed a relatively simple model with routinely available pre-treatment variables, to predict for neutropenia. This model should be independently validated prospectively.
AB - Objectives: Neutropenia is associated with the risk of life-threatening infections, chemotherapy dose reductions and delays that may compromise outcomes. This analysis was conducted to develop a prediction model for chemotherapy-induced severe neutropenia in lung cancer. Materials and Methods: Individual patient data from existing cooperative group phase II/III trials of stages III/IV non-small cell lung cancer or extensive small-cell lung cancer were included. The data were split into training and testing sets. In order to enhance the prediction accuracy and the reliability of the prediction model, lasso method was used for both variable selection and regularization on the training set. The selected variables was fit to a logistic model to obtain regression coefficients. The performance of the final prediction model was evaluated by the area under the ROC curve in both training and testing sets. Results: The dataset was randomly separated into training [7606 (67 %) patients] and testing [3746 (33 %) patients] sets. The final model included: age (>65 years), gender (male), weight (kg), BMI, insurance status (yes/unknown), stage (IIIB/IV/ESSCLC), number of metastatic sites (1, 2 or ≥3), individual drugs (gemcitabine, taxanes), number of chemotherapy agents (2 or ≥3), planned use of growth factors, associated radiation therapy, previous therapy (chemotherapy, radiation, surgery), duration of planned treatment, pleural effusion (yes/unknown), performance status (1, ≥2) and presence of symptoms (yes/unknown). Conclusions: We have developed a relatively simple model with routinely available pre-treatment variables, to predict for neutropenia. This model should be independently validated prospectively.
KW - Lung cancer
KW - Neutropenia
KW - Predictive models
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U2 - 10.1016/j.lungcan.2020.01.004
DO - 10.1016/j.lungcan.2020.01.004
M3 - Article
C2 - 31926983
AN - SCOPUS:85077657547
SN - 0169-5002
VL - 141
SP - 14
EP - 20
JO - Lung Cancer
JF - Lung Cancer
ER -