Evidence map›Paper›PMID 37861452›Full record

ArticleCancer discovery2024

AMG 509 (Xaluritamig), an Anti-STEAP1 XmAb 2+1 T-cell Redirecting Immune Therapy with Avidity-Dependent Activity against Prostate Cancer.

Olivier Nolan-Stevaux, Cong Li, Lingming Liang, Jinghui Zhan, Juan Estrada, Tao Osgood, Fei Li, Hanzhi Zhang, Ryan Case, Christopher M Murawsky and 14 more

Abstract read
PubMed Publisher
In one paragraph

Article in Cancer discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
11.1field-weighted citation impact, top 1% 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

36 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
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  5. T cell engagers in autoimmune diseases.Nature reviews. Immunology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 5 institutions in 5 countries.

Olivier Nolan-StevauxOncology Research, Amgen Research, Amgen Inc., South San Francisco, California.ORCID 0000-0002-5934-4786
Cong LiOncology Research, Amgen Research, Amgen Inc., South San Francisco, California.ORCID 0009-0000-0974-6675
Lingming LiangOncology Research, Amgen Research, Amgen Inc., South San Francisco, California.ORCID 0009-0008-5914-4603
Jinghui ZhanOncology Research, Amgen Research, Amgen Inc., Thousand Oaks, California.ORCID 0009-0002-1176-2249
Juan EstradaOncology Research, Amgen Research, Amgen Inc., Thousand Oaks, California.ORCID 0009-0002-3020-0292
Tao OsgoodOncology Research, Amgen Research, Amgen Inc., Thousand Oaks, California.ORCID 0009-0000-4393-0441
Fei LiStructural Biology, Amgen Research, Amgen Inc., South San Francisco, California.ORCID 0000-0003-0720-3129
Hanzhi ZhangStructural Biology, Amgen Research, Amgen Inc., South San Francisco, California.ORCID 0000-0002-5723-6116
Ryan CaseLead Discovery and Characterization, Amgen Research, Amgen Inc., South San Francisco, California.ORCID 0009-0006-8732-7250
Christopher M MurawskyTherapeutic Discovery, Amgen Research, Amgen Inc., Burnaby, Canada.ORCID 0000-0002-9698-052X
Bram EstesTherapeutic Discovery, Amgen Research, Thousand Oaks, California.ORCID 0000-0001-7968-3489
Gregory L MooreXencor, Inc., Pasadena, California.ORCID 0009-0003-2110-6461
Matthew J BernettXencor, Inc., Pasadena, California.ORCID 0000-0003-2103-5547
Umesh MuchhalXencor, Inc., Pasadena, California.ORCID 0000-0002-7791-0964
John R DesjarlaisXencor, Inc., Pasadena, California.ORCID 0000-0001-9726-021X
Binnaz K StaleyOncology Research, Amgen Research, Amgen Inc., South San Francisco, California.ORCID 0009-0007-6421-9836
Jennitte StevensTherapeutic Discovery, Amgen Research, Thousand Oaks, California.ORCID 0000-0002-4081-4696
Keegan S CookeOncology Research, Amgen Research, Amgen Inc., Thousand Oaks, California.ORCID 0000-0002-8509-1241
Famke AeffnerTranslational Safety and Bioanalytical Sciences, Amgen Research, Amgen Inc., South San Francisco, California.ORCID 0000-0002-1405-9228
Oliver ThomasTranslational Safety and Bioanalytical Sciences, Amgen Research (Munich) GmbH, Munich, Germany.ORCID 0009-0008-3327-2578
Julia StieglmaierEarly Development Oncology, Amgen Research (Munich) GmbH, Munich, Germany.ORCID 0009-0009-7035-5855
Jae-Lyun LeeAsan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.ORCID 0000-0002-9420-7162
Angela CoxonOncology Research, Amgen Research, Amgen Inc., Thousand Oaks, California.ORCID 0009-0000-3341-0645
Julie M BailisOncology Research, Amgen Research, Amgen Inc., South San Francisco, California.ORCID 0000-0002-0328-0322
Amgen (United States) · USEvorx (United States) · USAmgen (Germany) · DEBioanalytica (Switzerland) · CHUniversity of Ulsan · KR

Funding

n/a
6 · The paper itself

Abstract

The tumor-associated antigen STEAP1 is a potential therapeutic target that is expressed in most prostate tumors and at increased levels in metastatic castration-resistant prostate cancer (mCRPC). We developed a STEAP1-targeted XmAb 2+1 T-cell engager (TCE) molecule, AMG 509 (also designated xaluritamig), that is designed to redirect T cells to kill prostate cancer cells that express STEAP1. AMG 509 mediates potent T cell-dependent cytotoxicity of prostate cancer cell lines in vitro and promotes tumor regression in xenograft and syngeneic mouse models of prostate cancer in vivo. The avidity-driven activity of AMG 509 enables selectivity for tumor cells with high STEAP1 expression compared with normal cells. AMG 509 is the first STEAP1 TCE to advance to clinical testing, and we report a case study of a patient with mCRPC who achieved an objective response on AMG 509 treatment. SIGNIFICANCE: Immunotherapy in prostate cancer has met with limited success due to the immunosuppressive microenvironment and lack of tumor-specific targets. AMG 509 provides a targeted immunotherapy approach to engage a patient's T cells to kill STEAP1-expressing tumor cells and represents a new treatment option for mCRPC and potentially more broadly for prostate cancer. See related commentary by Hage Chehade et al., p. 20. See related article by Kelly et al., p. 76. This article is featured in Selected Articles from This Issue, p. 5.

Indexed as

Antibodies, BispecificProstatic Neoplasms, Castration-ResistantAnimalsAntigens, NeoplasmHumansImmunotherapyMaleMiceOxidoreductasesT-LymphocytesTumor MicroenvironmentAntibodies, BispecificAntigens, NeoplasmOxidoreductasesSTEAP1 protein, human

Identifiers

PMID37861452
OpenAlexW4387797966

What OpenQuestion holds

Textmetadata
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.