OSCR

Mapping intratumoral coverage of neural stem cell-delivered anti-HER2 antibody in breast cancer brain metastasis.

Overview

Authors: Jawad Fares1,2, Deepak Kanojia1,2, Edgar Petrosyan1,2, Alex L. Tobias1,2, Rafal Chojak1,2, Atique U. Ahmed1,2, Irina V. Balyasnikova1,2, Maciej S. Lesniak1,2
  1. Department of Neurological Surgery, Feinberg School of Medicine, Northwestern University,Chicago, IL USA
  2. Malnati Brain Tumor Institute, Robert H. Lurie Comprehensive Cancer Center, Northwestern University,Chicago, IL USA
Institutions: Northwestern University (United States)
Journal: Clinical & experimental metastasis, volume 43, issue 6, article 64
Dates: received 29 August 2026; accepted 3 November 2026; published online 10 November 2026; in print 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1007/s10585-026-10449-3 · PMID 43007545 · PMCID PMC13751723 · OpenAlex W7225696052
Open access: hybrid, a free copy (OpenAlex)
Status: code on request (how the code is found and verified)
Categories: human (organism), mouse (organism), other condition (population), developmental (subfield)
Methods: Connectivity, Statistics
Keywords: Breast cancer brain metastases, HER2, Neural stem cells, Antibody delivery, Tumor coverage, Cell-based therapy
MeSH: Brain Neoplasms*, Breast Neoplasms*, Erb-b2 Receptor Tyrosine Kinases*, Neural Stem Cells*, Animals, Cell Line, Tumor, Female, Humans, Mice, Xenograft Model Antitumor Assays (* major topic)
Topic: Glioma Diagnosis and Treatment (Oncology, Medicine), according to OpenAlex
Funding: National Cancer Institute (5R35CA283939-02)
Citations: not cited yet (Europe PMC); 57 references in the paper

Abstract

Cell-based therapies can formulate and deliver biologics within the brain, but their development has relied largely on survival outcomes that do not distinguish inadequate payload potency from inadequate tumor distribution. We evaluated intratumoral coverage as a quantitative endpoint for cell-mediated delivery using neural stem cells (NSCs) engineered to secrete an anti-HER2 antibody in breast cancer brain metastasis. Intracranial HER2-positive BT474Br tumors received a single dose of 5 × 105 anti-HER2 antibody-secreting NSCs. Secreted human IgG was reconstructed across consecutive 10-µm sections spanning the entire tumor depth, and therapeutic activity of the same cell dose administered once was assessed in an independent survival experiment. A single NSC dose produced a mean section-level antibody coverage of 60.6%; coverage was ≥ 25% in 96.8% of sections and ≥ 50% in 74.2%. Coverage was greatest in the tumor core and declined toward both poles, a pattern consistent with carrier-cell localization limiting therapeutic reach. The same dose extended median survival from 67 days with vector-control NSCs to 73.5 days (P = 0.0009) and increased restricted mean survival by 10.8 days. These data provide an initial spatial benchmark for a therapeutically active dose and establish tumor coverage as a mechanistically informative endpoint for intracranial cell-based delivery.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper says that its authors' code is available on request: it was not published with the paper, so there is nothing to verify.

The paper's code and data availability statement is in the Data section.

Tracing map

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Data

No dataset and no data link were found in the paper.

Data availability

The data generated in this study are available within the article. Analysis code used for the survival and spatial statistics is available upon reasonable request.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 12 November 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 8 authors, 6 keywords, 10 MeSH terms, 1 funder, 57 references.

Cite

This paper

Fares, J., Kanojia, D., Petrosyan, E., Tobias, A. L., Chojak, R., Ahmed, A. U., Balyasnikova, I. V., & Lesniak, M. S. (2026). Mapping intratumoral coverage of neural stem cell-delivered anti-HER2 antibody in breast cancer brain metastasis. Clinical & experimental metastasis, 43(6), 64. https://doi.org/10.1007/s10585-026-10449-3

BibTeX

@article{fares2026mapping,
author = {Fares, Jawad and Kanojia, Deepak and Petrosyan, Edgar and Tobias, Alex L. and Chojak, Rafal and Ahmed, Atique U. and Balyasnikova, Irina V. and Lesniak, Maciej S.},
title = {{Mapping intratumoral coverage of neural stem cell-delivered anti-HER2 antibody in breast cancer brain metastasis}},
journal = {Clinical \& experimental metastasis},
year = {2026},
month = nov,
volume = {43},
number = {6},
pages = {64},
publisher = {Springer Science+Business Media},
issn = {0262-0898},
doi = {10.1007/s10585-026-10449-3},
url = {https://doi.org/10.1007/s10585-026-10449-3},
pmid = {43007545},
pmcid = {PMC13751723}
}

RIS

TY - JOUR
AU - Fares, Jawad
AU - Kanojia, Deepak
AU - Petrosyan, Edgar
AU - Tobias, Alex L.
AU - Chojak, Rafal
AU - Ahmed, Atique U.
AU - Balyasnikova, Irina V.
AU - Lesniak, Maciej S.
TI - Mapping intratumoral coverage of neural stem cell-delivered anti-HER2 antibody in breast cancer brain metastasis
T2 - Clinical & experimental metastasis
J2 - Clin Exp Metastasis
PY - 2026
DA - 2026/11/10
VL - 43
IS - 6
SP - 64
SN - 0262-0898
PB - Springer Science+Business Media
DO - 10.1007/s10585-026-10449-3
UR - https://doi.org/10.1007/s10585-026-10449-3
LA - en
ER -

CSL-JSON

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