TY - JOUR
T1 - Predictors of Lung Adenocarcinoma With Leptomeningeal Metastases
T2 - A 2022 Targeted-Therapy-Assisted molGPA Model
AU - Zhang, Milan
AU - Tong, Jiayi
AU - Ma, Weifeng
AU - Luo, Chongliang
AU - Liu, Huiqin
AU - Jiang, Yushu
AU - Qin, Lingzhi
AU - Wang, Xiaojuan
AU - Yuan, Lipin
AU - Zhang, Jiewen
AU - Peng, Fuhua
AU - Chen, Yong
AU - Li, Wei
AU - Jiang, Ying
N1 - Publisher Copyright:
Copyright © 2022 Zhang, Tong, Ma, Luo, Liu, Jiang, Qin, Wang, Yuan, Zhang, Peng, Chen, Li and Jiang.
PY - 2022/6/10
Y1 - 2022/6/10
N2 - Objective: To explore prognostic indicators of lung adenocarcinoma with leptomeningeal metastases (LM) and provide an updated graded prognostic assessment model integrated with molecular alterations (molGPA). Methods: A cohort of 162 patients was enrolled from 202 patients with lung adenocarcinoma and LM. By randomly splitting data into the training (80%) and validation (20%) sets, the Cox regression and random survival forest methods were used on the training set to identify statistically significant variables and construct a prognostic model. The C-index of the model was calculated and compared with that of previous molGPA models. Results: The Cox regression and random forest models both identified four variables, which included KPS, LANO neurological assessment, TKI therapy line, and controlled primary tumor, as statistically significant predictors. A novel targeted-therapy-assisted molGPA model (2022) using the above four prognostic factors was developed to predict LM of lung adenocarcinoma. The C-indices of this prognostic model in the training and validation sets were higher than those of the lung-molGPA (2017) and molGPA (2019) models. Conclusions: The 2022 molGPA model, a substantial update of previous molGPA models with better prediction performance, may be useful in clinical decision making and stratification of future clinical trials.
AB - Objective: To explore prognostic indicators of lung adenocarcinoma with leptomeningeal metastases (LM) and provide an updated graded prognostic assessment model integrated with molecular alterations (molGPA). Methods: A cohort of 162 patients was enrolled from 202 patients with lung adenocarcinoma and LM. By randomly splitting data into the training (80%) and validation (20%) sets, the Cox regression and random survival forest methods were used on the training set to identify statistically significant variables and construct a prognostic model. The C-index of the model was calculated and compared with that of previous molGPA models. Results: The Cox regression and random forest models both identified four variables, which included KPS, LANO neurological assessment, TKI therapy line, and controlled primary tumor, as statistically significant predictors. A novel targeted-therapy-assisted molGPA model (2022) using the above four prognostic factors was developed to predict LM of lung adenocarcinoma. The C-indices of this prognostic model in the training and validation sets were higher than those of the lung-molGPA (2017) and molGPA (2019) models. Conclusions: The 2022 molGPA model, a substantial update of previous molGPA models with better prediction performance, may be useful in clinical decision making and stratification of future clinical trials.
KW - leptomeningeal metastases
KW - lung adenocarcinoma
KW - molGPA model
KW - overall survival
KW - targeted therapy
UR - http://www.scopus.com/inward/record.url?scp=85133695499&partnerID=8YFLogxK
U2 - 10.3389/fonc.2022.903851
DO - 10.3389/fonc.2022.903851
M3 - Article
C2 - 35795063
AN - SCOPUS:85133695499
SN - 2234-943X
VL - 12
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 903851
ER -