Skip to content
Research Article Open access CC BY 4.0

Leptomeningeal Metastasis: Current Treatment, and Emerging Therapies

Zain Jandial, Rachana Garg, Ashvin Kumar, Mike Chen

Journal of Cancer and Tumor International · pp. 15–29 · Published 29 Mar 2025

10.9734/jcti/2025/v15i2289

Abstract

Leptomeningeal carcinomatosis (LC) is a rare but devastating manifestation of cancer that has undergone metastatic spread to the cerebrospinal fluid and leptomeninges. The most common malignancies associated with LC are melanoma, breast, and lung cancers. LC severely influences morbidity and mortality, with a mean survival time of 2-6 months. Although characterized nearly 150 years ago, LC remains incurable as there are limited therapeutic options, and there is a considerable risk of treatment-related toxicities. Hence, there is an urgent need for thorough characterization of disease pathogenesis to determine novel therapeutic targets and strategies to reduce LC burden. Here, we review the current understanding of the molecular landscape of this disease and highlight recent advances in LC diagnosis and therapy. Graphical Abstract.: (A) Interaction between the breast cancer cell-secreted cytokine GM-CSF and the OPC-derived protein TPP1 within the leptomeningeal environment modulates Her2+LC growth and metastasis. (B) Derivation of primary Lepto cells, their implant in the PDX mouse model, isolation of cells, and subsequent culture to carry out the drug screen assay.

Leptomeningeal carcinomatosis HER2 breast cancer metastasis targeted-therapy GM-CSF KDM4A/4C

Cited by 0

No indexed citations yet.

Article metrics

Real usage data collected on this platform.

0

Page views

0

PDF downloads

0

Outbound clicks

0

Citations

Views by country

Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".

No views recorded yet.

Traffic sources

Referring site, by host.

No traffic recorded yet.

Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.