Evidence map›Paper›PMID 34767461›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2022

Blinatumomab Nonresponse and High-Disease Burden Are Associated With Inferior Outcomes After CD19-CAR for B-ALL.

Regina M Myers, Agne Taraseviciute, Seth M Steinberg, Adam J Lamble, Jennifer Sheppard, Bonnie Yates, Alexandra E Kovach, Brent Wood, Michael J Borowitz, Maryalice Stetler-Stevenson and 18 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed, 3 pooled it
13.7field-weighted citation impact, top 1% 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

130 citing papers in PubMed, 3 syntheses or guidelines pooled it, 198 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 9 institutions in 1 country.

Regina M MyersDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.ORCID 0000-0002-2542-2061
Agne TaraseviciuteSection of Transplantation and Cellular Therapy, Children's Hospital Los Angeles Cancer and Blood Disease Institute, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA.
Seth M SteinbergBiostatistics and Data Management Section, National Cancer Institute, National Institutes of Health, Bethesda, MD.ORCID 0000-0002-8280-551X
Adam J LambleDivision of Hematology and Oncology University of Washington, Seattle Children's Hospital, Seattle, WA.ORCID 0000-0002-7781-2918
Jennifer SheppardDivision of Pediatric Hematology-Oncology, Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX.
Bonnie YatesNational Cancer Institute/Center for Cancer Research, Pediatric Oncology Branch, National Institutes of Health, Bethesda, MD.
Alexandra E KovachSection of Transplantation and Cellular Therapy, Children's Hospital Los Angeles Cancer and Blood Disease Institute, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA.ORCID 0000-0002-6742-6749
Brent WoodSection of Transplantation and Cellular Therapy, Children's Hospital Los Angeles Cancer and Blood Disease Institute, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA.ORCID 0000-0001-7414-3969
Michael J BorowitzDepartment of Pathology, Johns Hopkins Hospital, Baltimore, MD.
Maryalice Stetler-StevensonLaboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Constance M YuanLaboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, MD.ORCID 0000-0002-2601-3665
Vinodh PillaiDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.ORCID 0000-0001-7126-6226
Toni FoleyNational Cancer Institute/Center for Cancer Research, Pediatric Oncology Branch, National Institutes of Health, Bethesda, MD.
Perry ChungDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.
Lee ChenSection of Transplantation and Cellular Therapy, Children's Hospital Los Angeles Cancer and Blood Disease Institute, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA.
Daniel W LeeDivision of Pediatric Hematology/Oncology, Department of Pediatrics, University of Virginia, Charlottesville, VA.ORCID 0000-0002-3249-9796
Colleen AnnesleyDivision of Hematology and Oncology University of Washington, Seattle Children's Hospital, Seattle, WA.
Amanda DiNofiaDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.ORCID 0000-0002-8321-0403
Stephan A GruppDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.ORCID 0000-0001-8030-7595
Samuel JohnDivision of Pediatric Hematology-Oncology, Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX.
Deepa BhojwaniDivision of Hematology/Oncology, Children's Hospital Los Angeles Cancer and Blood Disease Institute, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA.
Patrick A BrownDivision of Pediatric Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD.ORCID 0000-0002-8653-1069
Theodore W LaetschDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.ORCID 0000-0002-8497-3138
Lia GorePediatric Heme/Onc/BMT-CT, University of Colorado, Children's Hospital Colorado, Aurora, CO.ORCID 0000-0002-2546-4616
Rebecca A GardnerDivision of Hematology and Oncology University of Washington, Seattle Children's Hospital, Seattle, WA.
Susan R RheingoldDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.ORCID 0000-0001-8025-6767
Michael A PulsipherSection of Transplantation and Cellular Therapy, Children's Hospital Los Angeles Cancer and Blood Disease Institute, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA.ORCID 0000-0003-3030-8420
Nirali N ShahNational Cancer Institute/Center for Cancer Research, Pediatric Oncology Branch, National Institutes of Health, Bethesda, MD.ORCID 0000-0002-8474-9080
Children's Hospital of Philadelphia · USNational Institutes of Health · USUniversity of Southern California · USSeattle Children's Hospital · USSouthwestern Medical Center · USChildren's Hospital Colorado · USJohns Hopkins Hospital · USJohns Hopkins University · USUniversity of Virginia · US

Funding

Office of Collaborative BiostatisticsZIDSC007202 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI CHOO-WOSOBA, HYOYOUNG · 2009 to 2025
$14.5M
Immunotherapeutic approaches to treat pediatric hematologic malignanciesZIABC011823 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SHAH, NIRALI · 2019 to 2025
$6.1M
Intramural NIH HHS ZIA BC011823
6 · The paper itself

Abstract

purposeCD19-targeted chimeric antigen receptor T cells (CD19-CAR) and blinatumomab effectively induce remission in relapsed or refractory B-cell acute lymphoblastic leukemia (ALL) but are also associated with CD19 antigen modulation. There are limited data regarding the impact of prior blinatumomab exposure on subsequent CD19-CAR outcomes. PATIENTS AND

methodsWe conducted a multicenter, retrospective review of children and young adults with relapsed or refractory ALL who received CD19-CAR between 2012 and 2019. Primary objectives addressed 6-month relapse-free survival (RFS) and event-free survival (EFS), stratified by blinatumomab use. Secondary objectives included comparison of longer-term survival outcomes, complete remission rates, CD19 modulation, and identification of factors associated with EFS.

resultsOf 420 patients (median age, 12.7 years; interquartile range, 7.1-17.5) treated with commercial tisagenlecleucel or one of three investigational CD19-CAR constructs, 77 (18.3%) received prior blinatumomab. Blinatumomab-exposed patients more frequently harbored

conclusionWith the largest series to date in pediatric CD19-CAR, and, to our knowledge, the first to study the impact of sequential CD19 targeting, we demonstrate that blinatumomab nonresponse and high-disease burden were independently associated with worse RFS and EFS, identifying important indicators of long-term outcomes following CD19-CAR.

Indexed as

Antibodies, BispecificLymphoma, B-CellPrecursor Cell Lymphoblastic Leukemia-LymphomaAcute DiseaseAntigens, CD19ChildCost of IllnessHumansImmunotherapy, AdoptiveRecurrenceYoung AdultAntibodies, BispecificAntigens, CD19blinatumomab

Identifiers

PMID34767461
PMCPMC8937010
OpenAlexW3211722911

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.