Evidence map›Paper›PMID 37291203›Full record

ArticleNature communications2023

ALPL-1 is a target for chimeric antigen receptor therapy in osteosarcoma.

Nadia Mensali, Hakan Köksal, Sandy Joaquina, Patrik Wernhoff, Nicholas P Casey, Paola Romecin, Carla Panisello, René Rodriguez, Lene Vimeux, Asta Juzeniene and 17 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. LRRC15-CAR T Cells for the Treatment of Osteosarcoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Neoadjuvant Chemotherapy for Adults with Osteogenic Sarcoma.Current treatment options in oncology · 2024
    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

27 authors at 8 institutions in 6 countries.

Nadia MensaliTranslational Research Unit, Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway.ORCID 0000-0002-3130-4352
Hakan Köksal *Translational Research Unit, Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway.
Sandy Joaquina *Translational Research Unit, Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway.ORCID 0009-0005-8558-9399
Patrik WernhoffTranslational Research Unit, Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway.ORCID 0000-0002-8111-9841
Nicholas P CaseyTranslational Research Unit, Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway.
Paola RomecinJosep Carreras Leukemia Research Institute, Barcelona, Spain.
Carla PaniselloJosep Carreras Leukemia Research Institute, Barcelona, Spain.ORCID 0000-0002-8437-4418
René RodriguezInstituto de Investigación Sanitaria del Principado de Asturias (ISPA), Hospital Universitario Central de Asturias, Oviedo, Spain.ORCID 0000-0002-0768-7306
Lene VimeuxUniversité de Paris, Institut Cochin, INSERM, CNRS, Equipe labellisée Ligue Contre le Cancer, F-75014, PARIS, France.
Asta JuzenieneDepartment of Radiation Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Marit R MyhreTranslational Research Unit, Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway.
Anne FåneTranslational Research Unit, Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway.
Carolina Castilla RamírezInstitute of Biomedicine of Sevilla (IBiS), Virgen del Rocio University Hospital, CSIC, University of Sevilla, CIBER-ONC, 41013, Seville, Spain.
Solrun Melkorka MaggadottirTranslational Research Unit, Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway.
Adil Doganay DuruNSU Cell Therapy Institute, Dr. Kiran C. Patel College of Allopathic Medicine, Nova Southeastern University, Fort Lauderdale, FL, USA.ORCID 0000-0002-5844-913X
Anna-Maria GeorgoudakiNSU Cell Therapy Institute, Dr. Kiran C. Patel College of Allopathic Medicine, Nova Southeastern University, Fort Lauderdale, FL, USA.
Iwona GradDepartment of Radiation Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Andrés Daniel MaturanaLaboratory of Animal Cell Physiology, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Japan.
Gustav GaudernackDepartment of Cancer Immunology, Oslo University Hospital, Oslo, Norway.
Gunnar KvalheimTranslational Research Unit, Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway.
Angel M CarcabosoSJD Pediatric Cancer Center Barcelona, Institut de Recerca Sant Joan de Deu, Barcelona, 08950, Spain.ORCID 0000-0002-8485-426X
Enrique de AlavaInstitute of Biomedicine of Sevilla (IBiS), Virgen del Rocio University Hospital, CSIC, University of Sevilla, CIBER-ONC, 41013, Seville, Spain.ORCID 0000-0001-8400-046X
Emmanuel DonnadieuUniversité de Paris, Institut Cochin, INSERM, CNRS, Equipe labellisée Ligue Contre le Cancer, F-75014, PARIS, France.ORCID 0000-0002-4985-7254
Øyvind S BrulandDepartment of Oncology, Oslo University Hospital and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Pablo MenendezJosep Carreras Leukemia Research Institute, Barcelona, Spain.
Else Marit InderbergTranslational Research Unit, Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway. elsin@rr-research.no.
Sébastien WälchliTranslational Research Unit, Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway. sebastw@rr-research.no.ORCID 0000-0001-5869-1746
Oslo University Hospital · NOInstituto de Salud Carlos III · ESCentre National de la Recherche Scientifique · FRInstituto de Biomedicina de Sevilla · ESNova Southeastern University · USInstitució Catalana de Recerca i Estudis Avançats · ESInstitut de Recerca Sant Joan de DéuNagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS) remains a dismal malignancy in children and young adults, with poor outcome for metastatic and recurrent disease. Immunotherapies in OS are not as promising as in some other cancer types due to intra-tumor heterogeneity and considerable off-target expression of the potentially targetable proteins. Here we show that chimeric antigen receptor (CAR) T cells could successfully target an isoform of alkaline phosphatase, ALPL-1, which is highly and specifically expressed in primary and metastatic OS. The target recognition element of the second-generation CAR construct is based on two antibodies, previously shown to react against OS. T cells transduced with these CAR constructs mediate efficient and effective cytotoxicity against ALPL-positive cells in in vitro settings and in state-of-the-art in vivo orthotopic models of primary and metastatic OS, without unexpected toxicities against hematopoietic stem cells or healthy tissues. In summary, CAR-T cells targeting ALPL-1 show efficiency and specificity in treating OS in preclinical models, paving the path for clinical translation.

Indexed as

Bone NeoplasmsOsteosarcomaAlkaline PhosphataseCell Line, TumorChildHumansImmunotherapyImmunotherapy, AdoptiveT-LymphocytesAlkaline PhosphataseALPL protein, human

Identifiers

PMID37291203
PMCPMC10250459
OpenAlexW4379875529

What OpenQuestion holds

Textmetadata
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.