Evidence map›Paper›PMID 40919994›Full record

ArticleCancer research communications2025

Preclinical Evaluation of Folate Receptor-α Chimeric Antigen Receptor T Cells Exhibits Highly Efficient Antitumor Activity against Osteosarcoma.

Michelle Choe, Danielle Kirkey, Isabel Lira, Grace Hawkins, Melia Blankenfeld, Sarah Menashe, Rhonda E Ries, Brianna Wrightson, Christina Root, Cyd N McKay and 7 more

Registry-linked trialAbstract read
In one paragraph

Article in Cancer research communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06609928 (A Phase 1 Study of FOLR1 CAR T for Pediatric Patients With FOLR1/CBFA2T3), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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.

NCT06609928 phase1recruitingnot on this map

A Phase 1 Study of FOLR1 CAR T for Pediatric Patients With FOLR1/CBFA2T3::GLIS2+ Relapsed or Refractory AML

TypeinterventionalSponsorFred Hutchinson Cancer CenterRan2025 to 2042Enrolled12ConditionsRecurrent Childhood Acute Myeloid Leukemia, Refractory Childhood Acute Myeloid LeukemiaArmsFOLR1 CAR T-cells, Biospecimen Collection, Bone Marrow Aspiration, Bone Marrow Biopsy, Cyclophosphamide
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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

17 authors.

Michelle ChoeClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0000-0001-9850-9435
Danielle KirkeyCancer and Blood Disorder Center, Seattle Children's Hospital, Seattle, Washington.ORCID 0000-0001-5176-9416
Isabel LiraTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0009-0005-1514-2102
Grace HawkinsTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0009-0002-6253-078X
Melia BlankenfeldTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0009-0009-9762-7152
Sarah MenasheDepartment of Radiology, Seattle Children's Hospital, Seattle, Washington.ORCID 0000-0002-6016-2592
Rhonda E RiesTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0000-0002-3702-7923
Brianna WrightsonPreclinical Imaging Shared Resources, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0009-0009-6337-2198
Christina RootTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0009-0006-9145-3516
Cyd N McKayTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0009-0004-5124-5750
Jack H PeplinskiTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0000-0001-5097-0652
Raisa GlabmanComparative Pathology, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0000-0003-1492-8830
Lara E DavisKnight Cancer Institute, Oregon Health & Science University, Portland, Oregon.ORCID 0000-0002-6480-1611
Sanjay V MalhotraKnight Cancer Institute, Oregon Health & Science University, Portland, Oregon.ORCID 0000-0003-4056-5033
Richard GorlickDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-8995-2929
Elizabeth T LoggersClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0000-0003-3432-0443
Soheil MeshinchiTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington.ORCID 0000-0002-6276-4423

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
CAREER DEVELOPMENT IN PEDIATRIC AND MEDICAL ONCOLOGYK12CA076930 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DAVIDSON, NANCY ELLEN, MESHINCHI, SOHEIL · 1997 to 2025
$13.1M
PEDIATRIC ONCOLOGY RESEARCH TRAINING PROGRAMT32CA009351 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Elizabeth R Lawlor, SOHEIL MESHINCHI · 1985 to 2026
$7.0M
Fred Hutch Preclinical 3T MRIS10OD026919 · OD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HOLLAND, ERIC C. · 2020 to 2020
$600k
Kuni FoundationM.J. Murdock Charitable Trust (MJMCT) SR-20221337NCI NIH HHS K12 CA076930NCI NIH HHS P30 CA015704NCI NIH HHS T32 CA009351NIH HHS S10 OD026919Sam Day FoundationWipe Out Kids' Cancer (WOKC)
6 · The paper itself

Abstract

Metastatic and relapsed osteosarcoma remains difficult to treat despite advanced surgical techniques, intensified chemotherapy, and targeted therapies. Adoptive immunotherapies such as chimeric antigen receptor (CAR) T cells are in their nascent stage but remain a viable therapeutic strategy for patients with aggressive solid tumors such as osteosarcoma. Folate receptor-α (FOLR1) has been functionally implicated in osteosarcoma pathophysiology, providing rationale as a potential therapeutic target. We recently advanced a FOLR1-specific CAR T-cell product (FH FOLR1-CART) into a trial in infant acute myeloid leukemia (NCT06609928) and now evaluate this CAR construct against osteosarcoma. We provide comprehensive FOLR1 transcript and protein expression profile in patients with osteosarcoma, cell lines, and patient-derived xenografts, substantiating its significance as a therapeutic target. We further evaluate the in vitro and in vivo efficacy of FH FOLR1-CART in both standard and patient-derived osteosarcoma cell lines and xenograft models. FOLR1 transcript is expressed in the overwhelming majority of osteosarcoma primary patient specimens, osteosarcoma cell lines, and patient-derived models. FH FOLR1-CART exhibits robust in vitro activation and potent cytotoxicity against FOLR1-expressing osteosarcoma cell lines and primary osteosarcoma patient samples. More importantly, FH FOLR1-CART demonstrates potent antitumor activity in both localized and metastatic in vivo cell-derived and patient-derived xenograft models, with complete tumor eradication. These results demonstrate a potential therapeutic option for patients with advanced osteosarcoma. FH FOLR1-CART is advancing to an early-phase trial in relapsed/refractory osteosarcoma at Fred Hutchinson Cancer Center and Seattle Children's Hospital. SIGNIFICANCE: FOLR1 expression has previously been implicated in the pathogenesis of treatment-resistant osteosarcoma. This report demonstrates FOLR1 expression by most osteosarcoma tumors and provides preclinical evidence of robust antitumor activity both in vitro and in vivo against xenograft osteosarcoma models exhibited by FH FOLR1-CART. These data support ongoing efforts for clinical translation of FH FOLR1-CART to an early-phase clinical trial for patients with aggressive osteosarcoma.

Indexed as

Bone NeoplasmsFolate Receptor 1Immunotherapy, AdoptiveOsteosarcomaReceptors, Chimeric AntigenT-LymphocytesAnimalsCell Line, TumorFemaleHumansMaleMiceXenograft Model Antitumor AssaysFolate Receptor 1FOLR1 protein, humanReceptors, Chimeric Antigen

Identifiers

PMID40919994
PMCPMC12455178

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Registered trials

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.