Abstract

Several scoring systems are available to estimate prognosis and assist in selecting treatment methods for non-small cell lung cancer (NSCLC) patients with brain metastasis, including recursive partitioning analysis (RPA), basic score for brain metastases (BS-BM), and diagnosis-specific graded prognostic assessment (DS-GPA). Lung-molGPA is an update of the DS-GPA that incorporates EGFR and/or ALK mutation status. The present study tested the applicability of these four indexes in 361 lung adenocarcinoma patients with brain metastasis. Potential predictive factors in our independent multivariate analysis included patient age, Karnofsky performance status, EGFR and ALK mutation status, and use of targeted therapy. In the log-rank test, all four systems predicted overall survival (OS) (P<0.001). Harrell’s C indexes were 0.732, 0.724, 0.729, and 0.747 for RPA, BS-BM, DS-GPA, and Lung-molGPA, respectively. Our results confirmed that the Lung-molGPA index was useful for estimating OS in our patient cohort, and appeared to provide the most accurate predictions. However, the independent prognostic factors identified in our study were not entirely in agreement with the Lung-molGPA factors. In an era of targeted therapy, Lung-molGPA must be further updated to incorporate more specific prognostic factors based on additional patient data.

Highlights

  • Brain metastases are among the leading causes of morbidity and mortality in patients with non-small cell lung cancer (NSCLC) [1]

  • The diagnosis-specific graded prognostic assessment (DS-Graded Prognostic Assessment Index (GPA)) stratified patients with Brain metastasis (BM) by primary site and highlighted characteristics of tumors that metastasize to the brain, the various primary tumor genotypes did not fit within the prognostic classification system

  • By the end of the follow-up period for the 361 patients diagnosed with BMs from lung adenocarcinoma, 160 (44.3%) had confirmed epidermal growth factor receptor (EGFR) mutations and 10 (2.8%) had anaplastic lymphoma kinase-rearranged (ALK) mutations; one patient had both

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Summary

Introduction

Brain metastases are among the leading causes of morbidity and mortality in patients with non-small cell lung cancer (NSCLC) [1]. The prognosis for patients with BMs is generally poor; without treatment, median survival is estimated at 1–2 months. With whole brain radiotherapy (WBRT), the standard treatment for BMs regardless of histological subtype, median survival is 4–6 months [4, 5]. Accepted prognostic systems include, Recursive Partitioning Analysis (RPA), Basic Score for Brain Metastases (BS-BM), and the Graded Prognostic Assessment Index (GPA) [6,7,8]. Many cancers that commonly result in BMs, including NSCLC, small-cell lung cancer, breast cancer, melanoma, and renal carcinoma, involve different prognostic factors. Gene alterations were important prognostic factors for BMs [10,11,12,13]

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