Evidence map›Paper›PMID 35244681›Full record

Trial reportBlood advances2022

Outcome of donor-derived TAA-T cell therapy in patients with high-risk or relapsed acute leukemia post allogeneic BMT.

Hannah Kinoshita, Kenneth R Cooke, Melanie Grant, Maja Stanojevic, C Russell Cruz, Michael Keller, Maria Fernanda Fortiz, Fahmida Hoq, Haili Lang, A John Barrett and 15 more

Registry-linked trialOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02203903 (Multi-institutional Prospective Phase I Research of Expanded Multi-antigen Specifically Oriented Lymphocytes for the Treatment of VEry High Risk Hematopoietic Malignancies), which is not on this map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.5field-weighted citation impact, top 6% 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.

NCT02203903 phase1recruitingnot on this map

Multi-institutional Prospective Phase I Research of Expanded Multi-antigen Specifically Oriented Lymphocytes for the Treatment of VEry High Risk Hematopoietic Malignancies

TypeinterventionalSponsorCatherine BollardRan2015 to 2027Enrolled50ConditionsRelapsed/Refractory Hematopoietic Malignancies, Acute Myeloid Leukemia and MDSArmsTumor associated antigen lymphocytes (TAA-T)
3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 37 citations in OpenAlex.

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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

25 authors at 4 institutions in 1 country.

Hannah KinoshitaCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.ORCID 0000-0003-4106-1507
Kenneth R CookeDepartment of Oncology, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins University School of Medicine, Baltimore, MD.
Melanie GrantDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA.ORCID 0000-0002-5421-5889
Maja StanojevicCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
C Russell CruzCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Michael KellerCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Maria Fernanda FortizCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Fahmida HoqCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Haili LangCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.ORCID 0000-0001-8772-5984
A John BarrettStem Cell Transplantation and Cell Therapy Program, George Washington Cancer Center, Washington, DC.
Hua LiangDepartment of Statistics, The George Washington University, Washington, DC; and.
Jay TannaCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Nan ZhangCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Abeer ShibliCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Anushree DatarCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Kenneth FultonCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Divyesh KukadiyaCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Anqing ZhangDepartment of Pediatrics, The George Washington University School of Medicine and Health Sciences, Washington, DC.
Kirsten M WilliamsDepartment of Pediatric Hematology/Oncology, Aflac Cancer & Blood Disorders Center, Children's Healthcare of Atlanta and Emory University School of Medicine, Atlanta, GA.ORCID 0000-0001-9372-5286
Hema DaveCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.ORCID 0000-0001-5530-0201
Jeffrey S DomeCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.ORCID 0000-0002-9037-369X
David JacobsohnCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Patrick J HanleyCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Richard J JonesDepartment of Oncology, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins University School of Medicine, Baltimore, MD.
Catherine M BollardCenter for Cancer and Immunology Research, Children's National Research Institute, Children's National Hospital, Washington, DC.
Children's National · USEmory University · USGeorge Washington University · USJohns Hopkins University · US

Funding

TUMOR VACCINESP01CA015396 · NCI · JOHNS HOPKINS UNIVERSITY · PI HESS, ALLAN D · 1985 to 2016
$38.1M
Clinical and Translational Science Institute at Childrens NationalUL1TR001876 · NCATS · CHILDREN'S RESEARCH INSTITUTE · PI BELL, MICHAEL J · 2016 to 2021
$25.6M
Targeting MRDP01CA225618 · NCI · JOHNS HOPKINS UNIVERSITY · PI Lukasz Pawel Gondek · 2019 to 2026
$15.1M
Rationale for the Pediatric Hematology and Transfusion Medicine Multidisciplinary Research Training Award (PHTMMRT) at Children?s NationalT32HL110841 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI Catherine M. Bollard, NAOMI L LUBAN · 2012 to 2026
$2.0M
NCATS NIH HHS UL1 TR001876NCI NIH HHS P01 CA015396NCI NIH HHS P01 CA225618NHLBI NIH HHS T32 HL110841
6 · The paper itself

Abstract

Patients with hematologic malignancies relapsing after allogeneic blood or marrow transplantation (BMT) have limited response to conventional salvage therapies, with an expected 1-year overall survival (OS) of <20%. We evaluated the safety and clinical outcomes following administration of a novel T-cell therapeutic targeting 3 tumor-associated antigens (TAA-T) in patients with acute leukemia who relapsed or were at high risk of relapse after allogeneic BMT. Lymphocytes obtained from the BMT donor were manufactured to target TAAs WT1, PRAME, and survivin, which are over-expressed and immunogenic in most hematologic malignancies. Patients received TAA-T infusions at doses of 0.5 to 4 × 107/m2. Twenty-three BMT recipients with relapsed/refractory (n = 11) and/or high-risk (n = 12) acute myeloid leukemia (n = 20) and acute lymphoblastic leukemia (n = 3) were infused posttransplant. No patient developed cytokine-release syndrome or neurotoxicity, and only 1 patient developed grade 3 graft-versus-host disease. Of the patients who relapsed post-BMT and received bridging therapy, the majority (n = 9/11) achieved complete hematologic remission before receiving TAA-T. Relapsed patients exhibited a 1-year OS of 36% and 1-year leukemia-free survival of 27.3% post-TAA-T. The poorest prognosis patients (relapsed <6 months after transplant) exhibited a 1-year OS of 42.8% postrelapse (n = 7). Median survival was not reached for high-risk patients who received preemptive TAA-T posttransplant (n = 12). Although as a phase 1 study, concomitant antileukemic therapy was allowed, TAA-T were safe and well tolerated, and sustained remissions in high-risk and relapsed patients were observed. Moreover, adoptively transferred TAA-T detected by T-cell receptor V-β sequencing persisted up to at least 1 year postinfusion. This trial was registered at clinicaltrials.gov as #NCT02203903.

Indexed as

Hematologic NeoplasmsHematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcutePrecursor Cell Lymphoblastic Leukemia-LymphomaAcute DiseaseBone Marrow TransplantationHumansRecurrence

Identifiers

PMID35244681
PMCPMC9043933
OpenAlexW4214831141

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.