drugset / Trial / NCT05289908

Summary

Intrathecal chemotherapy is one of the most important treatment modalities for leptomeningeal metastasis of solid tumors. In the previous study(Intrathecal Pemetrexed for Recurrent Leptomeningeal Metastasis From Non-small Cell Lung Cancer: A Prospective Pilot Clinical Trial. ClinicalTrials.gov identification number: NCT03101579), pemetrexed presented feasibility of intrathecal administration. Pemetrexed at 10 mg dose level on the schedule of 1-2 times per week was recommended as an intrathecal administration agent for patients with refractory leptomeningeal metastases from non-small-cell lung cancer in the previous study. Moreover, the maximum-tolerated dose and recommended dose of intrathecal pemetrexed in the previous study was obtained without vitamin supplementation. Vitamin supplementation has been shown to reduce pemetrexed-induced myelosuppression. In this study, the regimen of intrathecal pemetrexed with folic acid and vitamin B12 supplementation may provide higher safety. Therefore, the purpose of this study is to investigate the maximally tolerated dose and evaluate the safety and effectiveness of intrathecal pemetrexed with vitamin supplementation as the first-line intrathecal chemotherapy in patients with leptomeningeal metastases from malignant solid tumors.

Timeline

Start
2022-02-21
Primary completion
2023-03-20
Completion
2024-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Pemetrexed Small molecule 15 mg Intrathecal
Subject Pemetrexed Small molecule 20 mg Intrathecal
Subject Pemetrexed Small molecule 25 mg Intrathecal
Background Dexamethasone Small molecule 5 mg Intrathecal
Background Vitamin B12 Other / unclassified 1000 ug Intramuscular
Background folic acid Other / unclassified 200 ug Oral
Background folic acid Other / unclassified 400 ug Oral