Evidence map›Paper›PMID 42666451›Full record

ArticleFrontiers in immunology2026

The LVI Component Hypothesis: the lymphatic-to-vascular invasion ratio as an enrichment biomarker for therapy with PD-L1×VEGF-A bispecific antibodies.

Kenneth A Kern

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

1 author.

Kenneth A KernAffiliate Faculty, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, San Diego, CA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphovascular invasion (LVI) describes intravasated tumor cells within intratumoral lymphatic or blood vessels. LVI is reported routinely on pathologic examination because it is prognostic for reduced disease-free and overall survival across many solid tumors. In contrast, it is not considered a predictive biomarker because its presence cannot discriminate which patients benefit from a given therapy. To become predictive, a biomarker must reflect the aberrant, specific biology a drug targets. Bispecific antibodies with functional arms against immunologic and vascular targets are a recent class of biologics that simultaneously engage the malignant immunologic and angiogenic components of a tumor. In this setting, deconstructing LVI into its invasive lymphatic and vascular components, and expressing their ratio, is hypothesized to add predictive capability to this histologic finding. LVI-positive tumors are enriched for parameters relevant to both arms of this class of bispecific antibodies. Immunologically, they carry higher tumor mutational burden, more frequent PD-L1 expression, and TGF-β signaling. Angiogenically, blood vessel invasion reflects a VEGF-A-driven, disordered, T-cell-excluding vasculature. The author proposes the LVI Component Hypothesis, which is that tumor cell intravasation into lymphatic versus blood vessels can be expressed as a ratio, the lymphatic-to-vascular invasion ratio (LVR). This ratio may predict benefit from PD-L1×VEGF-A bispecific antibodies. No clinical data currently link the LVR to response, so it is presented as a hypothesis to be tested, first in archived tissue from completed trials of PD-L1×VEGF-A bispecific antibodies and then in prospective randomized trials. If validated, the LVR might help to select those patients most likely to respond, raising the response rate among those treated and possibly sparing those unlikely to benefit.

Indexed as

Antibodies, BispecificB7-H1 AntigenBiomarkers, TumorLymphatic VesselsNeoplasmsVascular Endothelial Growth Factor AAnimalsHumansLymphatic MetastasisNeoplasm InvasivenessNeovascularization, PathologicAntibodies, BispecificB7-H1 AntigenBiomarkers, TumorCD274 protein, humanVascular Endothelial Growth Factor Abispecific antibodiesimmune checkpoint inhibitorslymphatic vesselslymphovascular invasionpredictive biomarkerprogrammed death-ligand 1tumor microenvironmentvascular endothelial growth factor A

Identifiers

PMID42666451
PMCPMC13522231

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.