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โ† Trials
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Intrathecal Pemetrexed for Leptomeningeal Metastasis in EGFR-Mutant NSCLC

RecruitingPhase 2Ages 20 Years - anyAllTaipei Veterans General Hospital, Taiwan
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In plain words

What the trial is, and whether it could suit you

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 ex

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๐Ÿ“‹ Eligibility rules (as published)
Inclusion criteria * At least 20 years of age. * Patients with metastatic non-squamous NSCLC harboring known EGFR activating mutation and with a diagnosis of probable or confirmed LM by the European Association of Neuro-Oncology-European Society for Medical Oncology (EANO-ESMO) guideline. \[5\] EGFR activating mutations include exon19 deletion, T790M, L858R, G719X, L861Q, or S768I. * Intracranial disease progression after osimertinib use, proved by contrast-enhanced MRI * Stable extra-cranial disease status, judged by investigators. * Eastern Cooperative Oncology Group (ECOG) performance status 0-3 and a minimum life expectancy of 12 weeks * Normal bone marrow and organ function as defined below: * Marrow: Hemoglobin โ‰ฅ9gm/dL, ANC โ‰ฅ1500/mm3 platelets โ‰ฅ100,000/mm3 * Hepatic: Serum total bilirubin โ‰ค1.5 x upper limit of normal (ULN), ALT (SGPT) and AST (SGOT) โ‰ค3 x ULN. * Renal: Creatinine clearance (Ccr) โ‰ฅ45 mL/min. * For female patients of childbearing potential, agreement (by patient and/or partner) to use a highly effective form(s) of contraception that results in a low failure rate (\< 1% per year) when used consistently and correctly, and to continue its use for 5 months after the last dose of IP. Such methods include: combined (estrogen and progestogen containing) hormonal contraception, progestogen-only hormonal contraception associated with inhibition of ovulation together with another additional barrier method always containing a spermicide, intrauterine device (IUD), intrauterine hormone-releasing system (IUS), bilateral tubal occlusion, vasectomized partner (on the understanding that this is the only one partner during the whole study duration), and sexual abstinence. * Ability to understand and willingness to sign an IRB approved written informed consent document. * Willing to provide CSF and plasma samples for ctDNA analysis. Exclusion criteria * Uncontrolled extra-CNS disease which needs other systemic treatment than EGFR-TKI. * Uncontrolled tumor-related pain * Uncontrolled or symptomatic hypercalcemia (\> 1.5 mmol/L ionized calcium or Ca \> 12 mg/dL or corrected serum calcium \> ULN). Patients who are receiving denosumab prior to study enrollment must be willing and eligible to receive a bisphosphonate instead while in the study. * Malignancies other than NSCLC within 5 years prior to study enrollment, with the exception of those with a negligible risk of metastasis or death (e.g., expected 5-year OS \> 90%) treated with expected curative outcome (such as adequately treated carcinoma in situ of the cervix, basal or squamous-cell skin cancer, localized prostate cancer treated surgically with curative intent, ductal carcinoma in situ treated surgically with curative intent) * On chronic systemic steroid therapy more than 20 mg prednisolone per day (or equivalent) or on any other form of immunosuppressive medication * Has received a live-virus vaccination within 30 days of planned treatment start * Systemic cytotoxic chemotherapy or major surgery within 2 weeks of the first dose of study medication * Active infection requiring therapy * History of Human Immunodeficiency Virus (HIV) infection. * Hepatitis B carrier: Patients with HBV infection were required to be receiving effective antiviral therapy and have a viral load less than 100 IU/mL at screening * Active Hepatitis C * Has received intrathecal chemotherapy within 2 weeks before the start of IP * Has received whole-brain radiotherapy (WBRT) within 2 weeks before the start of IP * Uncontrolled epilepsy * History of allergic reaction to intravenous pemetrexed. * Severe coagulation abnormality (INR \> 2). * Severe symptomatic hydrocephalus that requires other treatment modalities other than IP * Bulky intra-cranial lesion that requires other treatment modalities other than IP
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What it tests

  • Pemetrexed
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Where

1 site
Department of Chest Medicine, Taipei Veterans General Hospital
Taipei, Taiwan
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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