Science news and articles on health, environment, global warming, stem cells, bird flu, autism, nanotechnology, dinosaurs, evolution -- the latest discoveries in astronomy, anthropology, biology, chemistry, climate & bioengineering, computers, engineering ; medicine, math, physics, psychology, technology, and more from the world's leading research centers universities.

Leptomeningeal metastases more common in NSCLC patients with EGFR mutations


DENVER – Leptomeningeal metastases (LM), a devastating complication and predictor of poor survival in lung cancer patients, was found to be more prevalent in non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) mutations. Patients receiving tyrosine kinase inhibitors (TKIs) targeting EGFR mutations had a longer overall survival (OS) than those who did not receive TKIs, demonstrating the effectiveness of TKIs for LM therapy.

The leptomeninges are the membranes that surround the brain, including the arachnoid mater and pia mater, and ensue when cancer cells metastasize to intracranial structures and the cerebrospinal fluid (CSF). LM occurs in 10-26% of lung cancer and the presence of LM is a devastating complication for patients and often associated with poor survival. Treatment strategies for LM include epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs), chemotherapy, whole brain radiotherapy (WBRT), intrathecal chemotherapy (ITC), surgery, and ventriculoperitoneal (VP) shunt operations. However, therapeutic options for treating LM are challenging with no standard treatment. The use of EGFR-TKIs markedly prolong survival in patients with EGFR mutations and frequent EGFR mutations.

A group of Chinese investigators retrospectively screened 5,387 NSCLC patients at Guangdong Lung Cancer Institute, Guangdong General Hospital, from January 2011 to June 2015 to examine the prevalence of EGFR mutations in NSCLC patients with LM as well as treatments and clinical outcomes. Medical records of patients were reviewed for demographics, tumor-related features, and major treatments. Patients with known EGFR status were screened for LM by cerebrospinal fluid (CSF) cytology test or gadolinium-enhanced brain magnetic resonance imaging (MRI). OS was determined from the period of LM diagnosis to death or last follow-up. OS was estimated using the Kaplan-Meier method and presented as a median value with a two-sided 95% confidence interval (CI).

The results of the study published in the Journal of Thoracic Oncology, the official journal of the International Association for the Study of Lung Cancer (IASLC), showed that of the 5,387 patients examined only 3,775 patients were tested for EGFR gene status. Of those tested for EGFR status, 1,258 patients had confirmed EGRF mutations and 2,517 had wild-type EGFR (no identified mutations). The incidence of LM in all 5,387 patients was 3.4% (184/5,387). However, the incidence of patients with LM harboring EGFR mutations (9.4%, 118/1258) were significantly more than those with a wild-type EGFR status (1.7%, 42/2,517; χ2 = 122.9, p

Patients that were given TKIs for treatment of LM had longer OS than patients that did not take TKIs (10 months, 95% CI=8.9-11.1 vs. 3.3 months, 95% CI = 0.5-6.1; p

The authors comment that, "This study had some limitations, however, we showed that OS after LM was longer than that in previous reports, and LM were much more frequent in NSCLC patients harboring EGFR mutations. EGFR-TKIs were the optimal strategy for LM with EGFR mutations, especially TKI treatment-naÏve patients. Nevertheless, active treatment with WBRT, with or without EGFR-TKIs, was not supported by our study."


Co-authors Ben-Yuan Jiang, Jin-Ji Yang, Hai-Yan Tu, Qing Zhou, Wei-Bang Guo, Yi-Long Wu are members of IASLC.

About the IASLC:

The International Association for the Study of Lung Cancer (IASLC) is the only global organization dedicated to the study of lung cancer. Founded in 1974, the association's membership includes more than 5,000 lung cancer specialists in over 100 countries. Visit for more information.

Written by: Jacinta Wiens, PhD, 720-598-1941; [email protected]

Media Contact: Jeff Wolf, 720-325-2952; [email protected]

Media Contact

Jeff Wolf
[email protected]

Leave A Reply

Your email address will not be published.