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Article: Intrathecal nivolumab and IL-2 for treatment of leptomeningeal metastases in EGFR-mutated lung adenocarcinoma

TitleIntrathecal nivolumab and IL-2 for treatment of leptomeningeal metastases in EGFR-mutated lung adenocarcinoma
Authors
Issue Date18-May-2025
PublisherElsevier
Citation
Lung Cancer, 2025, v. 204 How to Cite?
Abstract

Objectives

Leptomeningeal metastasis (LM) is a serious complication of advanced non-small-cell lung cancer (NSCLC). Intrathecal administration of nivolumab or interleukin-2 (IL-2) has demonstrated efficacy in this setting. Preclinical and limited clinical evidence suggest that combining IL-2 with anti-PD1 therapy may synergistically enhance anti-tumor immunity. However, clinical data on the efficacy and safety of intrathecal co-administration of nivolumab and IL-2 are lacking.

Materials and Methods

We describe a case of NSCLC with LM, refractory to multiple EGFR tyrosine kinase inhibitors and previous intrathecal therapies, treated with intrathecal nivolumab and IL-2. Single-cell RNA sequencing (scRNA-seq) was performed on cerebrospinal fluid (CSF) samples collected before and after treatment.

Results

This is the first reported case of intrathecal nivolumab plus IL-2 in NSCLC with LM resistant to standard systemic and intrathecal therapies. The patient experienced marked clinical improvement, including substantial remission of intracranial metastases, neurological symptom relief, and a reduction in tumor marker levels, without notable treatment-related adverse events. scRNA-seq analysis of CSF revealed a post-treatment decrease in malignant cell populations and a concomitant increase in immune effector cells, particularly CD8+ T cells and NK cells. Malignant cells exhibited upregulated antigen presentation and apoptosis. Cell-cell interaction analysis indicated enhanced NK cell-mediated cytotoxicity via FASL-FAS signaling and reduced immunosuppressive interactions between regulatory CD4+ T cells and effector memory CD8+ T cells.

Conclusions

This case report provides preliminary evidence supporting the feasibility, safety, and potential efficacy of intrathecal nivolumab and IL-2 in treating NSCLC-associated LM. These findings warrant further investigation in prospective clinical studies.


Persistent Identifierhttp://hdl.handle.net/10722/356531
ISSN
2023 Impact Factor: 4.5
2023 SCImago Journal Rankings: 1.761
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorRuan, Zhaohui-
dc.contributor.authorZeng, Liang-
dc.contributor.authorZhang, Jin-
dc.contributor.authorQin, Haoyue-
dc.contributor.authorHuang, Zhe-
dc.contributor.authorYan, Huan-
dc.contributor.authorZhang, Gao-
dc.contributor.authorZhang, Yongchang-
dc.date.accessioned2025-06-04T00:40:16Z-
dc.date.available2025-06-04T00:40:16Z-
dc.date.issued2025-05-18-
dc.identifier.citationLung Cancer, 2025, v. 204-
dc.identifier.issn0169-5002-
dc.identifier.urihttp://hdl.handle.net/10722/356531-
dc.description.abstract<h3>Objectives</h3><p>Leptomeningeal metastasis (LM) is a serious complication of advanced non-small-cell lung cancer (NSCLC). Intrathecal administration of nivolumab or interleukin-2 (IL-2) has demonstrated efficacy in this setting. Preclinical and limited clinical evidence suggest that combining IL-2 with anti-PD1 therapy may synergistically enhance anti-tumor immunity. However, clinical data on the efficacy and safety of intrathecal co-administration of nivolumab and IL-2 are lacking.</p><h3>Materials and Methods</h3><p>We describe a case of NSCLC with LM, refractory to multiple EGFR tyrosine kinase inhibitors and previous intrathecal therapies, treated with intrathecal nivolumab and IL-2. Single-cell RNA sequencing (scRNA-seq) was performed on cerebrospinal fluid (CSF) samples collected before and after treatment.</p><h3>Results</h3><p>This is the first reported case of intrathecal nivolumab plus IL-2 in NSCLC with LM resistant to standard systemic and intrathecal therapies. The patient experienced marked clinical improvement, including substantial remission of intracranial metastases, neurological symptom relief, and a reduction in tumor marker levels, without notable treatment-related adverse events. scRNA-seq analysis of CSF revealed a post-treatment decrease in malignant cell populations and a concomitant increase in immune effector cells, particularly CD8<sup>+</sup> T cells and NK cells. Malignant cells exhibited upregulated antigen presentation and apoptosis. Cell-cell interaction analysis indicated enhanced NK cell-mediated cytotoxicity via FASL-FAS signaling and reduced immunosuppressive interactions between regulatory CD4<sup>+</sup> T cells and effector memory CD8<sup>+</sup> T cells.</p><h3>Conclusions</h3><p>This case report provides preliminary evidence supporting the feasibility, safety, and potential efficacy of intrathecal nivolumab and IL-2 in treating NSCLC-associated LM. These findings warrant further investigation in prospective clinical studies.</p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofLung Cancer-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleIntrathecal nivolumab and IL-2 for treatment of leptomeningeal metastases in EGFR-mutated lung adenocarcinoma-
dc.typeArticle-
dc.identifier.doi10.1016/j.lungcan.2025.108586-
dc.identifier.volume204-
dc.identifier.eissn1872-8332-
dc.identifier.isiWOS:001499375700001-
dc.identifier.issnl0169-5002-

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