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Intrathecal Pemetrexed for Leptomeningeal Metastasis in EGFR-Mutant NSCLC

StatusRecruiting
PhasePhase 2
Started
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Record History

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  1. Notable Trial status: Not Yet Recruiting to Recruitingv3 Show 4 more changesShow less
    • Primary completion date: Jun 1, 2026 to Dec 31, 2026
    • Study sites: 0 to 1
    • Study completion date: Jun 1, 2027 to Dec 31, 2027
    • Start date changed from estimate of Jun 1, 2024 to Aug 1, 2024
  2. Notable Primary completion date: May 1, 2025 to Jun 1, 2026v2 Show 4 more changesShow less
    • Start date: May 1, 2023 to Jun 1, 2024
    • Study completion date: May 1, 2025 to Jun 1, 2027
    • Eligibility criteria expanded, about 60 words
    • Secondary endpoints: details revised at 1 of 3 entries
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Leptomeningeal metastasis (LM) is a complication of advanced non-small cell lung cancer (NSCLC). The incidence of LM in NSCLC patients is around 3-5 %, reaching 9.4 % of those with an epidermal growth factor receptor (EGFR) mutation. Generally, the efficacy of systemic treatment for LM is limited due to the blood-brain barrier. Osimertinib has a high central nervous system penetration rate, making it the preferred first-line treatment for EGFR-mutant NSCLC. Previous studies indicated that osimertinib had shown promising efficacy in pretreated patients harboring EGFR mutations and LM. However, intracranial disease progression eventually develops, and the prognosis of patients with LM progression after osimertinib is poor. Recently, intrathecal chemotherapy with pemetrexed (IP) was reported to be an alternative treatment in patients with NSCLC and LM. The results from a phase I/II trial examining the efficacy and safety of IP in patients with EGFR-mutant NSCLC after the failure of previous TKI, and 83% of study enrollees received osimertinib before IP. The clinical response rate was 84.6%, and the median overall survival was 9.0 months. Despite initial promising efficacy, further trials are needed to verify these results. Therefore, the investigators plan to conduct a prospective study to examine the safety and effectiveness of IP combined with EGFR-TKI for patients with EGFR mutant NSCLC after osimertinib failure.
Trial Details
NCT Number NCT05805631
Lead Sponsor Taipei Veterans General Hospital, Taiwan
Conditions
(from sponsor)
Carcinoma, Non-Small-Cell Lung, Epidermal Growth Factor Receptor, Leptomeningeal Metastasis
Related terms Carcinoma, Non-Small-Cell Lung, Meningeal Carcinomatosis
Enrollment 23 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov