Efficacy evaluation of tyrosine kinase inhibitors for advanced non-small cell lung cancer patients with leptomeningeal metastasis
- Yanhua Wang 1,2,3, Yue Hao 4, Manyi Xu 1,2,3, Lue Hong 5, Chunwei Xu 3, Zhengbo Song 2,3
- Yanhua Wang 1,2,3, Yue Hao 4, Manyi Xu 1,2,3
- 1The Second Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou, China.
- 2Department of Clinical Trial, Zhejiang Cancer Hospital, Hangzhou, China.
- 3Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Hangzhou, China.
- 4Department of Respiratory Medicine, Affiliated Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
- 5The First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China.
- 0The Second Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou, China.
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View abstract on PubMed
Summary
This summary is machine-generated.Targeted therapy shows promise for non-small cell lung cancer (NSCLC) with leptomeningeal metastasis (LM). Concurrent local therapy significantly improved progression-free and overall survival in these challenging NSCLC patients.
Area Of Science
- Oncology
- Medical Research
- Clinical Trials
Background
- Leptomeningeal metastasis (LM) is a rare but serious complication of non-small cell lung cancer (NSCLC).
- Standardized treatment protocols for NSCLC with LM are lacking.
- This study evaluates targeted therapy's efficacy and safety in NSCLC patients with LM.
Purpose Of The Study
- To assess the effectiveness of targeted therapy in non-small cell lung cancer patients with leptomeningeal metastasis.
- To provide data for improved treatment strategies for this patient group.
- To analyze factors influencing progression-free survival in NSCLC with LM.
Main Methods
- Retrospective analysis of 193 non-small cell lung cancer patients with leptomeningeal metastasis.
- Patients received targeted therapy, with some also receiving concurrent leptomeningeal local therapy (chemotherapy or radiotherapy).
- Diagnosis confirmed via cerebrospinal fluid cytology, MRI, and clinical symptoms.
Main Results
- Median progression-free survival (mPFS) was 6.9 months; median overall survival (mOS) was 15.0 months.
- Concurrent local leptomeningeal therapy significantly improved mPFS (11.4 vs. 6.5 months) and mOS (18.1 vs. 13.6 months).
- Performance status, treatment lines, angiogenesis inhibitors, and local therapy were independent factors influencing PFS.
Conclusions
- Targeted therapies offer encouraging outcomes for NSCLC patients with LM.
- Concurrent local leptomeningeal therapy enhances survival benefits in this population.
- Further research is warranted to optimize treatment strategies for NSCLC with LM.
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