An Open-label, Single-arm, Phase II Trial of Intrathecal Pemetrexed for Leptomeningeal Metastasis From Lung Adenocarcinoma That Progressed After a Double Dose of Third-generation TKIs, Including Osimertinib

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Pemetrexed is one of the first-line chemotherapeutic agents for non-squamous non-small cell lung cancer (NSCLC). Since 2017, intrathecal pemetrexed has shown good efficacy for patients with leptomeningeal metastases from NSCLC. It has been recommended as the preferred drug for intrathecal chemotherapy by the Chinese Society of Clinical Oncology (CSCO) guidelines. Tyrosine kinase inhibitors (TKIs) play a promising role in treating non-small cell lung cancer patients with epidermal growth factor receptor (EGFR) mutations. An international multi-center clinical study published in 2019 confirmed that double dose of osimertinib showed significant improvement in leptomeningeal metastases from NSCLC with EGFR exon 19 deletion or exon 21 L858R/T790M mutation. It makes TKIs the mainstay of treatment for patients with EGFR-mutant NSCLC with leptomeningeal metastases. However, the choice of treatment after resistance to targeted therapy is a hot topic in clinical practice, with 78% of patients in the study above who responded to double-dose osimertinib still showing progression at the time of follow-up. The purpose of this study was to observe the safety and efficacy of intrathecal pemetrexed for leptomeningeal metastasis from lung adenocarcinoma that progressed after a double dose of a third-generation TKI such as osimertinib.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Male or female aged between 18 and 75 years.

• Histologically or cytologically confirmed diagnosis of NSCLC with single activating EGFR mutations (L858R or Exon19Del).

• Confirmed diagnosis of leptomeningeal metastasis according to ESMO/ EANO guidelines.

• Progression after previous double doses of third-generation TKIs such as Osimertinib.

• Normal liver and kidney function; WBC≥4000/mm3, Plt≥100000/mm3.

• No history of severe nervous system disease.

• No severe dyscrasia.

Locations
Other Locations
China
The Affiliated Huizhou Hospital, Guangzhou Medical University
RECRUITING
Huizhou
Contact Information
Primary
Zhenyu Pan
dr-zypan@163.com
+8615804302753
Backup
Guozi Yang
guoziyang_1982@163.com
+8615804302755
Time Frame
Start Date: 2025-09-01
Estimated Completion Date: 2027-03-20
Participants
Target number of participants: 36
Treatments
Experimental: Group
Intra-pemetrexed
Sponsors
Leads: Guangzhou Medical University

This content was sourced from clinicaltrials.gov