Evidence map›Paper›PMID 33246985›Full record

ArticleJournal for immunotherapy of cancer2020

Diagnostic approach to the evaluation of myeloid malignancies following CAR T-cell therapy in B-cell acute lymphoblastic leukemia.

George Mo, Hao-Wei Wang, Aimee C Talleur, Shilpa A Shahani, Bonnie Yates, Haneen Shalabi, Michael G Douvas, Katherine R Calvo, Jack F Shern, Sridhar Chaganti and 8 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 28 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

18 authors at 9 institutions in 2 countries.

George MoPediatric Oncology Branch, National Cancer Institute, Bethesda, Maryland, USA.
Hao-Wei WangLaboratory of Pathology, National Cancer Institute, Bethesda, Maryland, USA.
Aimee C TalleurDepartment of Bone Marrow Transplantation and Cellular Therapy, St Jude Children's Research Hospital, Memphis, Tennessee, USA.
Shilpa A ShahaniPediatric Oncology Branch, National Cancer Institute, Bethesda, Maryland, USA.
Bonnie YatesPediatric Oncology Branch, National Cancer Institute, Bethesda, Maryland, USA.
Haneen ShalabiPediatric Oncology Branch, National Cancer Institute, Bethesda, Maryland, USA.ORCID 0000-0001-8692-8034
Michael G DouvasDepartment of Hematology/Oncology, Emily Couric Clinical Cancer Center, University of Virginia, Charlottesville, Virginia, USA.
Katherine R CalvoDepartment of Laboratory Medicine, National Institutes of Health, Bethesda, Maryland, USA.
Jack F ShernPediatric Oncology Branch, National Cancer Institute, Bethesda, Maryland, USA.
Sridhar ChagantiCentre for Clincal Haematology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Katharine PatrickSheffield Children's Hospital NHS Foundation Trust, Sheffield, UK.
Young SongOncogenomics Section, National Cancer Institute, Bethesda, Maryland, USA.
Terry J FryUniversity of Colorado Anschutz Medical Campus and Center for Cancer and Blood Disorders, Children's Hospital of Colorado, Aurora, Colorado, USA.
Xiaolin WuCancer Research Technology Program, Leidos Biomedical Research, Inc, Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA.
Brandon M TriplettDepartment of Bone Marrow Transplantation and Cellular Therapy, St Jude Children's Research Hospital, Memphis, Tennessee, USA.
Javed KhanOncogenomics Section, National Cancer Institute, Bethesda, Maryland, USA.
Rebecca A GardnerSeattle Children's Hospital, Seattle, Washington, USA.
Nirali N ShahPediatric Oncology Branch, National Cancer Institute, Bethesda, Maryland, USA nirali.shah@nih.gov.ORCID 0000-0002-8474-9080
National Cancer Institute · USSt. Jude Children's Research Hospital · USCenter for Cancer and Blood Disorders · USLeidos (United States) · USNational Institutes of Health · USSeattle Children's Hospital · USSheffield Children's NHS Foundation Trust · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBUniversity of Virginia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapeutic strategies targeting B-cell acute lymphoblastic leukemia (B-ALL) effectively induce remission; however, disease recurrence remains a challenge. Due to the potential for antigen loss, antigen diminution, lineage switch or development of a secondary or treatment-related malignancy, the phenotype and manifestation of subsequent leukemia may be elusive. We report on two patients with multiply relapsed/refractory B-ALL who, following chimeric antigen receptor T-cell therapy, developed myeloid malignancies. In the first case, a myeloid sarcoma developed in a patient with a history of myelodysplastic syndrome. In the second case, two distinct events occurred. The first event represented a donor-derived myelodysplastic syndrome with monosomy 7 in a patient with a prior hematopoietic stem cell transplantation. This patient went on to present with lineage switch of her original B-ALL to ambiguous lineage T/myeloid acute leukemia. With the rapidly evolving field of novel immunotherapeutic strategies, evaluation of relapse and/or subsequent neoplasms is becoming increasingly more complex. By virtue of these uniquely complex cases, we provide a framework for the evaluation of relapse or evolution of a subsequent malignancy following antigen-targeted immunotherapy.

Indexed as

AdolescentAdultFemaleHumansImmunotherapyMalePrecursor Cell Lymphoblastic Leukemia-LymphomaReceptors, Chimeric AntigenT-LymphocytesYoung AdultReceptors, Chimeric Antigenadoptivechimeric antigenimmunotherapyreceptors

Identifiers

PMID33246985
PMCPMC7703409
OpenAlexW3108772849

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.