» Articles » PMID: 27243238

Concurrent Radiotherapy and Intrathecal Methotrexate for Treating Leptomeningeal Metastasis from Solid Tumors with Adverse Prognostic Factors: A Prospective and Single-arm Study

Overview
Journal Int J Cancer
Specialty Oncology
Date 2016 Jun 1
PMID 27243238
Citations 40
Authors
Affiliations
Soon will be listed here.
Abstract

The prognosis of leptomeningeal metastasis (LM) from solid tumors is extremely poor, especially for patients with adverse prognostic factors. In this phase II clinical trial, we evaluated the efficacy and safety of intrathecal chemotherapy (IC) combined with concomitant involved-field radiotherapy (IF-RT) for treating LM from solid tumors with adverse prognostic factors. Fifty-nine patients with LM from various solid tumors were enrolled between May 2010 and December 2014. Concurrent therapy consisted of concomitant IC (methotrexate 12.5-15 mg and dexamethasone 5 mg, weekly) and IF-RT (whole brain and/or spinal canal RT, 40 Gy/20f). For patients with low Karnofsky performance status (KPS) score and radiotherapy intolerance, induction IC (1-3 times) was given before concurrent therapy. Thirty-eight patients (64.4%) received subsequent treatments. All patients were followed up at least 6 months after LM diagnosis or until death. Primary endpoint evaluated was clinical response rate. Secondary endpoints were overall survival (OS) and safety. The pathological types included lung cancer (n = 42), breast cancer (n = 11) and others (n = 6). Median KPS score was 40 (range 20-70). Fifty-one patients (86.4%) completed concurrent therapy. The overall response rate was 86.4% (51/59). OS ranged from 0.4 to 36.7 months (median 6.5 months), and 1-year-survival rate was 21.3%. Treatment-related adverse events mainly included acute meningitis, chronic-delayed encephalopathy, radiculitis, myelosuppression and mucositis. Twelve patients (20.3%) had grade III-V toxic reactions. We concluded that IC combined with concomitant IF-RT, with significant efficacy and acceptable toxicity, may be an optimal therapeutic option for treatment of LM from solid tumors with adverse prognostic factors. LM, in which cancer cells spread to membranes enveloping the brain and spinal cord, is a devastating complication of solid cancers. Existing LM therapies center on IC. In this prospective clinical study, the authors combined intrathecal methotrexate with involved-field radiotherapy in a concomitant regimen, showing that the approach can potentially improve quality of life for patients with adverse prognostic factors. Concurrent radiotherapy-bolstered IC by contributing to prolonged remission of neurological symptoms and increasing OS. The findings suggest that the concomitant regimen could be an optimal treatment option for LM.

Citing Articles

The research progress on meningeal metastasis in solid tumors.

Yue Y, Ren Y, Lu C, Jiang N, Wang S, Fu J Discov Oncol. 2025; 16(1):254.

PMID: 40019647 PMC: 11871263. DOI: 10.1007/s12672-025-01950-4.


A review on intrathecal administration of medications for leptomeningeal metastases in solid tumors.

Wang X, Yao C, Quan L, Zhou J Front Pharmacol. 2025; 16:1472945.

PMID: 39981182 PMC: 11841460. DOI: 10.3389/fphar.2025.1472945.


Current Evidence in the Systemic Treatment of Brain Metastases from Breast Cancer and Future Perspectives on New Drugs, Combinations and Administration Routes: A Narrative Review.

Garrone O, Ruatta F, Rea C, Denaro N, Ghidini M, Cauchi C Cancers (Basel). 2025; 16(24.

PMID: 39766062 PMC: 11675070. DOI: 10.3390/cancers16244164.


Intrathecal pemetrexed improves survival outcomes in previously treated EGFR-mutant advanced non-small-cell lung cancer with leptomeningeal metastases.

Li L, Huang Z, Chen Y, Ma H, Chen X, Yan H Heliyon. 2025; 10(24):e40703.

PMID: 39759323 PMC: 11696667. DOI: 10.1016/j.heliyon.2024.e40703.


Leptomeningeal metastatic disease: new frontiers and future directions.

Ozair A, Wilding H, Bhanja D, Mikolajewicz N, Glantz M, Grossman S Nat Rev Clin Oncol. 2024; 22(2):134-154.

PMID: 39653782 DOI: 10.1038/s41571-024-00970-3.


References
1.
Sause W, Crowley J, Eyre H, Rivkin S, PUGH R, QUAGLIANA J . Whole brain irradiation and intrathecal methotrexate in the treatment of solid tumor leptomeningeal metastases--a Southwest Oncology Group study. J Neurooncol. 1988; 6(2):107-12. DOI: 10.1007/BF02327385. View

2.
Boogerd W, van den Bent M, Koehler P, Heimans J, van der Sande J, Aaronson N . The relevance of intraventricular chemotherapy for leptomeningeal metastasis in breast cancer: a randomised study. Eur J Cancer. 2004; 40(18):2726-33. DOI: 10.1016/j.ejca.2004.08.012. View

3.
Chamberlain M, Soffietti R, Raizer J, Ruda R, Brandsma D, Boogerd W . Leptomeningeal metastasis: a Response Assessment in Neuro-Oncology critical review of endpoints and response criteria of published randomized clinical trials. Neuro Oncol. 2014; 16(9):1176-85. PMC: 4136900. DOI: 10.1093/neuonc/nou089. View

4.
Bleyer W . Current status of intrathecal chemotherapy for human meningeal neoplasms. Natl Cancer Inst Monogr. 1977; 46:171-8. View

5.
Hitchins R, Bell D, Woods R, LEVI J . A prospective randomized trial of single-agent versus combination chemotherapy in meningeal carcinomatosis. J Clin Oncol. 1987; 5(10):1655-62. DOI: 10.1200/JCO.1987.5.10.1655. View