Evidence map›Paper›PMID 32210091›Full record

ArticleCancers2020

LRRC15 Targeting in Soft-Tissue Sarcomas: Biological and Clinical Implications.

Eytan Ben-Ami, Raul Perret, Ying Huang, Félicie Courgeon, Prafulla C Gokhale, Audrey Laroche-Clary, Benjamin K Eschle, Valérie Velasco, François Le Loarer, Marie-Paule Algeo and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  4. LRRC15-CAR T Cells for the Treatment of Osteosarcoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
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  11. GPX1 expression promotes stemness and aggressiveness in myxoid liposarcomas.International journal of biological sciences · 2025
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 2 countries.

Eytan Ben-AmiSarcoma Division, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Raul PerretDepartment of Pathology, Institut Bergonié, 33000 Bordeaux, France.ORCID 0000-0003-2698-0249
Ying HuangSarcoma Division, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Félicie CourgeonSarcoma Unit, Institut Bergonié, 33000 Bordeaux, France.
Prafulla C GokhaleSarcoma Division, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Audrey Laroche-ClarySarcoma Unit, Institut Bergonié, 33000 Bordeaux, France.
Benjamin K EschleSarcoma Division, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Valérie VelascoDepartment of Pathology, Institut Bergonié, 33000 Bordeaux, France.
François Le LoarerDepartment of Pathology, Institut Bergonié, 33000 Bordeaux, France.
Marie-Paule AlgeoUniversity of Bordeaux, 33400 Talence, France.
James PurcellAbbVie Biotherapeutics, Redwood City, CA 94063, USA.
George D DemetriSarcoma Division, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Antoine ItalianoSarcoma Unit, Institut Bergonié, 33000 Bordeaux, France.
Dana-Farber Cancer Institute · USInstitut Bergonié · FRInserm · FRUniversité de Bordeaux · FRAbbVie (United States) · USHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLRRC15 is a member of the LRR (leucine-rich repeat) superfamily present on tumor-associated fibroblasts (CAFs) and stromal cells. The expression of LRRC15 is upregulated by the pro-inflammatory cytokine TGFβ. ABBV-085 is a monomethyl auristatin E (MMAE)-containing antibody-drug conjugate (ADC) designed to target LRRC15, and which has shown significant anti-tumor activity in several tumor models. This is the first focused examination of LRRC15 expression and ABBV-085 activity in soft-tissue sarcomas (STS).

methodsWe analyzed the LRRC15 expression profile by immunohistochemistry in 711 STS cases, covering a broad spectrum of STS histologies and sub-classifications. In vivo experiments were carried out by using LRRC15-positive and LRRC15-negative patient-derived xenograft (PDX) models of STS.

resultsIn contrast to patterns observed in epithelial tumors, LRRC15 was expressed not only by stromal cells but also by cancer cells in multiple subsets of STS with significant variations noted between histological subtypes. Overexpression of LRRC15 is positively correlated with grade and independently associated with adverse outcome. ABBV-085 has robust preclinical efficacy against LRRC15 positive STS patient-derived xenograft (PDX) models.

conclusionWe provide the first preclinical evidence that LRRC15 targeting with an antibody-drug conjugate is a promising strategy in LRRC15-positive STS. ABBV-085 is being evaluated in an ongoing clinical trial in STS and other malignancies.

Indexed as

ABBV-085LRRC15sarcoma

Identifiers

PMID32210091
PMCPMC7140027
OpenAlexW3012659663

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.