Abstract

BackgroundBrain metastasis (BM) is a poor prognostic factor for non-small-cell lung cancer (NSCLC). The efficacy and roles of combining temozolomide (TMZ) with whole brain radiotherapy (WBRT) in protection neurocognitive function (NCF) and improvement quality of life (QOL) were investigated and compared with WBRT alone in the treatment of NSCLC patients with BM.MethodsA total of 238 NSCLC patients with BM were reviewed and categorized into WBRT plus TMZ (RCT) arm and WBRT alone (RT), respectively. The efficacy was evaluated with Pearson chi-square or Fisher’s exact tests, Log-rank test and Cox proportional hazards model. NCF was assessed by using revised Hopkins Verbal Learning Test (HVLT-R), Controlled Oral Word Association (COWA) test and Trail-making Test (TMT). QOL was assessed by the Functional Assessment of Cancer Treatment-Lung (FACT-L) Chinese version 4.0 questionnaire.ResultsThe average intracranial objective response (ORR) and disease control rate (DCR) for all the patients were 26.9 and 95.8%, respectively. The intracranial ORR and DCR for RCT and RT arm were 34.9% vs. 20.2% (p = 0.01) and 98.4% vs. 92.7% (p = 0.03), respectively. The median intracranial progression-free survival (PFS) and overall survival (OS) of NSCLC patients with BM were 5.2 and 7.3 months, respectively. The median PFS of RCT arm was significantly longer than that of RT arm (5.9 vs. 4.9 months, p = 0.002). The median OS of the RCT arm was also slightly longer than that of the RT arm (8.5 vs. 5.9 months), but without statistical significance (p = 0.11). Multivariate analysis indicated that TMZ was a significant factor for PFS. Statistically significant differences on NCF and QOL were observed between CRT and RT arms at 5 months. RCT showed a trend of toxicities increase compared with RT, however, the toxicities were tolerable and manageable.ConclusionsAdding TMZ to WBRT in the treatment of NSCLC patients with BM could improve the intracranial ORR, DCR, and median PFS compared with WBRT alone. Although no remarkable difference on median OS was found, adding TMZ could prevent NCF and QOL from worsening. The side effects increased by adding TMZ, but the difference was not statistical significance and toxicities were well tolerated.

Highlights

  • Brain metastasis (BM) is a poor prognostic factor for non-small-cell lung cancer (NSCLC)

  • Adding TMZ to whole brain radiotherapy (WBRT) in the treatment of NSCLC patients with BM could improve the intracranial objective response rate (ORR), disease control rate (DCR), and median progression-free survival (PFS) compared with WBRT alone

  • The eligibility criteria for this study were as follows: patients were historically diagnosed with NSCLC and had confirmed BM by magnetic resonance imaging (MRI); had at least one measurable BM with diameter larger than 10 mm; patients had no history of Tyrosine Kinase Inhibitor (TKIs) administration; had adequate function of major organs and hematologic function; had no uncontrolled morbidities; with Eastern Cooperative Oncology Group performance status ≤3; Treated by WBRT with a prescription of 3 Gy/fraction × 10 fractions

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Summary

Introduction

Brain metastasis (BM) is a poor prognostic factor for non-small-cell lung cancer (NSCLC). The efficacy and roles of combining temozolomide (TMZ) with whole brain radiotherapy (WBRT) in protection neurocognitive function (NCF) and improvement quality of life (QOL) were investigated and compared with WBRT alone in the treatment of NSCLC patients with BM. Temozolomide (TMZ) is a new oral alkylating agent, which is able to cross the brain blood barrier with demonstrated survival benefit in the treatment of high-grade gliomas when administered concurrently with adjuvant radiotherapy [11]. The purpose of this study is to investigate the survival benefits, neurocognitive function (NCF) and quality of life (QOL) influence of WBRT with or without TMZ in the treatment of NSCLC patients with BM

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