Evidence map›Paper›PMID 33619171›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

The B7-H3-Targeting Antibody-Drug Conjugate m276-SL-PBD Is Potently Effective Against Pediatric Cancer Preclinical Solid Tumor Models.

Nathan M Kendsersky, Jarrett Lindsay, E Anders Kolb, Malcolm A Smith, Beverly A Teicher, Stephen W Erickson, Eric J Earley, Yael P Mosse, Daniel Martinez, Jennifer Pogoriler and 13 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed, 1 pooled it
7.6field-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

81 citing papers in PubMed, 1 synthesis or guideline pooled it, 118 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Preclinical Activity of the B7-H3-Targeting Antibody-Drug Conjugate Vobramitamab Duocarmazine in Pediatric Solid Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Targeted therapies in pediatric oncology: A start.Molecular therapy. Oncology · 2026
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. D3-GPC2-Directed CAR T Cells Are Safe and Efficacious in Preclinical Models of Neuroblastoma and Small Cell Lung Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  18. Review
  19. Review
  20. Article

21 more citing papers are in PubMed but not listed here.

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

23 authors at 7 institutions in 1 country.

Nathan M Kendsersky *Division of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Pennsylvania.
Jarrett Lindsay *Division of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Pennsylvania.
E Anders KolbA.I. duPont Hospital for Children, Wilmington, Delaware.
Malcolm A SmithNCI Cancer Therapy Evaluation Program, Bethesda, Maryland.ORCID 0000-0001-9880-9876
Beverly A TeicherNCI Cancer Therapy Evaluation Program, Bethesda, Maryland.
Stephen W EricksonRTI International, Research Triangle Park, North Carolina.
Eric J EarleyRTI International, Research Triangle Park, North Carolina.ORCID 0000-0001-6576-1319
Yael P MosseDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Pennsylvania.ORCID 0000-0002-3463-0399
Daniel MartinezDivision of Anatomic Pathology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Jennifer PogorilerPerelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0001-9366-4401
Kateryna KrytskaDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Pennsylvania.
Khushbu PatelDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Pennsylvania.ORCID 0000-0002-3269-7442
David GroffDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Pennsylvania.
Matthew TsangDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Pennsylvania.
Samson GhiluGreehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
Yifei WangDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Steven SeamanTumor Angiogenesis Unit, Mouse Cancer Genetics Program (MCGP), NCI-Frederick, Frederick, Maryland.
Yang FengTumor Angiogenesis Unit, Mouse Cancer Genetics Program (MCGP), NCI-Frederick, Frederick, Maryland.
Brad St CroixTumor Angiogenesis Unit, Mouse Cancer Genetics Program (MCGP), NCI-Frederick, Frederick, Maryland.
Richard GorlickDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-8995-2929
Raushan KurmashevaGreehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, Texas.ORCID 0000-0003-3212-2363
Peter J HoughtonGreehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, Texas. maris@chop.edu houghtonp@uthscsa.edu.
John M MarisDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Pennsylvania. maris@chop.edu houghtonp@uthscsa.edu.ORCID 0000-0002-8088-7929
Children's Hospital of Philadelphia · USFrederick National Laboratory for Cancer Research · USThe University of Texas Health Science Center at San Antonio · USNational Cancer Institute · USRTI International · USThe University of Texas MD Anderson Cancer Center · USCommunity Health Systems - Dupont Hospital · US

Funding

Targeting TEMs in Preclinical Tumor ModelsZIABC010578 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ST CROIX, BRADLEY D · 2009 to 2025
$16.2M
Discovering mechanisms of neuroblastoma tumorigenesis to improve patient outcomesR35CA220500 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI JOHN M MARIS · 2017 to 2026
$8.7M
Osteosarcoma: Patient Derived Xenograft Preclinical TestingU01CA199221 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Richard G. Gorlick · 2015 to 2026
$3.8M
Pediatric Preclinical Testing Consortium: Research Programs Non-CNS (U01)U01CA199297 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HOUGHTON, PETER J · 2015 to 2021
$3.5M
A Testing Program to Identify Novel Agents for Treatment of Pediatric and AYA High-Risk Sarcoma, Kidney and Liver CancerU01CA263981 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Raushan Kurmasheva · 2021 to 2026
$3.2M
Pediatric Preclinical Testing Consortium: Coordinating Center-Additional PPTC funding extensionU01CA199222 · NCI · RESEARCH TRIANGLE INSTITUTE · PI GATTO, GREGORY J · 2015 to 2021
$2.6M
Pediatric Preclinical Testing ConsortiumU01CA199287 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI MARIS, JOHN M · 2015 to 2021
$2.1M
Characterizing ALCAM as an oncoprotein and immunotherapeutic target in neuroblastomaF31CA254244 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LINDSAY, JARRETT · 2020 to 2022
$126k
Credentialing Delta-like 3 (DLL3) as an oncoprotein and immunotherapeutic target in neuroblastomaF31CA239424 · NCI · UNIVERSITY OF PENNSYLVANIA · PI KENDSERSKY, NATHAN MICHAEL · 2020 to 2022
$121k
NCI NIH HHS F31 CA239424NCI NIH HHS F31 CA254244NCI NIH HHS R35 CA220500NCI NIH HHS U01 CA199221NCI NIH HHS U01 CA199222NCI NIH HHS U01 CA199287NCI NIH HHS U01 CA199297NCI NIH HHS U01 CA263981
6 · The paper itself

Abstract

purposePatients with relapsed pediatric solid malignancies have few therapeutic options, and many of these patients die of their disease. B7-H3 is an immune checkpoint protein encoded by the EXPERIMENTAL

designB7-H3 expression was quantified by RNA sequencing and by IHC on pediatric PDX microarrays. We tested the safety and efficacy of m276-SL-PBD in two stages. Randomized trials of m276-SL-PBD of 0.5 mg/kg on days 1, 8, and 15 compared with vehicle were performed in PDX or CDX models of Ewing sarcoma (

resultsThe vast majority of PDX and CDX samples studied showed intense membranous B7-H3 expression (median H-score 177, SD 52). In the randomized trials, m276-SL-PBD showed a 92.3% response rate, with 61.5% of models showing a maintained complete response (MCR). These data were confirmed in the single mouse trial with an overall response rate of 91.5% and MCR rate of 64.4%. Treatment-related mortality rate was 5.5% with late weight loss observed in a subset of models dosed once a week for 3 weeks.

conclusionsm276-SL-PBD has significant antitumor activity across a broad panel of pediatric solid tumor PDX models.

Indexed as

AnimalsB7 AntigensCell Line, TumorChildDisease Models, AnimalFemaleHumansImmunoconjugatesMiceNeoplasmsPediatricsTreatment OutcomeXenograft Model Antitumor AssaysB7 AntigensCD276 protein, humanImmunoconjugates

Identifiers

PMID33619171
PMCPMC8127361
OpenAlexW3129393016

What OpenQuestion holds

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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.