Evidence map›Paper›PMID 38163318›Full record

ArticleBlood advances2024

Durable immunity to EBV after rituximab and third-party LMP-specific T cells: a Children's Oncology Group study.

Birte Wistinghausen, Keri Toner, Donald A Barkauskas, Lauren P Jerkins, Hannah Kinoshita, Pamela Chansky, Gloria Pezzella, Lauren Saguilig, Robert J Hayashi, Harshal Abhyankar and 7 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02900976 (A Pilot Study of Rituximab), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.8field-weighted citation impact, top 8% 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.

NCT02900976 phase2completednot on this map

A Pilot Study of Rituximab (RTX) and Third Party Latent Membrane Protein (LMP)-Specific Cytotoxic T-Lymphocytes (LMP-TC) in Pediatric Solid Organ Recipients (SOT) With EBV-Positive CD20-Positive Post-Transplant Lymphoproliferative Disease (PTLD)

TypeinterventionalSponsorChildren's Oncology GroupRan2017 to 2025Enrolled18ConditionsEBV-Related Post-Transplant Lymphoproliferative Disorder, Monomorphic Post-Transplant Lymphoproliferative Disorder, Polymorphic Post-Transplant Lymphoproliferative Disorder, Recurrent Monomorphic Post-Transplant Lymphoproliferative DisorderArmsAllogeneic LMP1/LMP2-Specific Cytotoxic T-Lymphocytes, Rituximab
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Adoptive T-cell therapy for virus-associated diseases.Clinical microbiology reviews · 2025
    Review
  4. Review
  5. Article
  6. Review
  7. Virus-Specific T-Cell Therapy for the Management of Viral Infections in the Immunocompromised.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2025
    Review
  8. Review
  9. Article
  10. EBV and post-transplant lymphoproliferative disorder: a complex relationship.Hematology. American Society of Hematology. Education Program · 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

17 authors at 7 institutions in 1 country.

Birte WistinghausenCenter for Cancer and Blood Disorders, Children's National Hospital, Washington, DC.ORCID 0000-0002-2874-121X
Keri TonerCenter for Cancer and Blood Disorders, Children's National Hospital, Washington, DC.ORCID 0000-0002-9324-7314
Donald A BarkauskasDepartment of Population and Public Health Sciences, Keck School of Medicine of the University of Southern California, Los Angeles, CA.ORCID 0000-0002-2339-719X
Lauren P JerkinsDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN.
Hannah KinoshitaCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.ORCID 0000-0003-4106-1507
Pamela ChanskyThe George Washington University School of Medicine and Health Sciences, Washington, DC.ORCID 0000-0002-8169-992X
Gloria PezzellaCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Lauren SaguiligChildren's Oncology Group Statistics and Data Center, Monrovia, CA.
Robert J HayashiDivision of Pediatric Hematology/Oncology, Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO.
Harshal AbhyankarBaylor College of Medicine, Texas Children's Hospital Cancer Center, Houston, TX.
Brooks ScullBaylor College of Medicine, Texas Children's Hospital Cancer Center, Houston, TX.
Vivekanudeep KarriRush Medical College, Chicago, IL.
Jay TannaCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Patrick HanleyCenter for Cancer and Blood Disorders, Children's National Hospital, Washington, DC.
Michelle L HermistonDepartment of Pediatrics, Benioff Children's Hospital and the Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA.ORCID 0000-0003-1790-2679
Carl E AllenBaylor College of Medicine, Texas Children's Hospital Cancer Center, Houston, TX.
Catherine M BollardCenter for Cancer and Blood Disorders, Children's National Hospital, Washington, DC.
Children's National · USBaylor College of Medicine · USUniversity of Southern California · USGeorge Washington University · USSt. Jude Children's Research Hospital · USSt. Louis Children's Hospital · USUniversity of California, San Francisco · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Tissue ResourceP50CA126752 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Leonid S Metelitsa · 2007 to 2026
$51.4M
NCI NIH HHS P50 CA126752NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

abstractPosttransplant lymphoproliferative disease (PTLD) in pediatric solid organ transplant (SOT) recipients is characterized by uncontrolled proliferation of Epstein-Barr virus-infected (EBV+) B cells due to decreased immune function. This study evaluated the feasibility, safety, clinical and immunobiological outcomes in pediatric SOT recipients with PTLD treated with rituximab and third-party latent membrane protein-specific T cells (LMP-TCs). Newly diagnosed (ND) patients without complete response to rituximab and all patients with relapsed/refractory (R/R) disease received LMP-TCs. Suitable LMP-TC products were available for all eligible subjects. Thirteen of 15 patients who received LMP-TCs were treated within the prescribed 14-day time frame. LMP-TC therapy was generally well tolerated. Notable adverse events included 3 episodes of rejection in cardiac transplant recipients during LMP-TC therapy attributed to subtherapeutic immunosuppression and 1 episode of grade 3 cytokine release syndrome. Clinical outcomes were associated with disease severity. Overall response rate (ORR) after LMP-TC cycle 1 was 70% (7/10) for the ND cohort and 20% (1/5) for the R/R cohort. For all cohorts combined, the best ORR for LMP-TC cycles 1 and 2 was 53% and the 2-year overall survival was 70.7%. vβT-cell receptor sequencing showed persistence of adoptively transferred third-party LMP-TCs for up to 8 months in the ND cohort. This study establishes the feasibility of administering novel T-cell therapies in a cooperative group clinical trial and demonstrates the potential for positive outcomes without chemotherapy for ND patients with PTLD. This trial was registered at www.clinicaltrials.gov as #NCT02900976 and at the Children's Oncology Group as ANHL1522.

Indexed as

Epstein-Barr Virus InfectionsLymphoproliferative DisordersChildHerpesvirus 4, HumanHumansRituximabT-LymphocytesRituximab

Identifiers

PMID38163318
PMCPMC10909726
OpenAlexW4390483091

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.