Evidence map›Paper›PMID 33081391›Full record

ReviewInternational journal of molecular sciences2020

Facts and Challenges in Immunotherapy for T-Cell Acute Lymphoblastic Leukemia.

Fátima Bayón-Calderón, María L Toribio, Sara González-García

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.8field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 60 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

3 authors at 1 institution in 1 country.

Fátima Bayón-CalderónInteractions with the Environment Program, Immune System Development and Function Unit, Centro de Biología Molecular Severo Ochoa, CSIC-UAM, 28049 Madrid, Spain.ORCID 0000-0001-6662-4594
María L ToribioInteractions with the Environment Program, Immune System Development and Function Unit, Centro de Biología Molecular Severo Ochoa, CSIC-UAM, 28049 Madrid, Spain.ORCID 0000-0002-8637-0373
Sara González-GarcíaInteractions with the Environment Program, Immune System Development and Function Unit, Centro de Biología Molecular Severo Ochoa, CSIC-UAM, 28049 Madrid, Spain.ORCID 0000-0002-0315-2136
Centro de Biología Molecular Severo Ochoa · ES

Funding

Fundación Asociación Española Contra el Cáncer CICPF18030TORIMinisterio de Ciencia e Innovación (Agencia Estatal de Investigación/European Regional Development Fund, European Union) SAF2016-75442-R
6 · The paper itself

Abstract

T-cell acute lymphoblastic leukemia (T-ALL), a T-cell malignant disease that mainly affects children, is still a medical challenge, especially for refractory patients for whom therapeutic options are scarce. Recent advances in immunotherapy for B-cell malignancies based on increasingly efficacious monoclonal antibodies (mAbs) and chimeric antigen receptors (CARs) have been encouraging for non-responding or relapsing patients suffering from other aggressive cancers like T-ALL. However, secondary life-threatening T-cell immunodeficiency due to shared expression of targeted antigens by healthy and malignant T cells is a main drawback of mAb-or CAR-based immunotherapies for T-ALL and other T-cell malignancies. This review provides a comprehensive update on the different immunotherapeutic strategies that are being currently applied to T-ALL. We highlight recent progress on the identification of new potential targets showing promising preclinical results and discuss current challenges and opportunities for developing novel safe and efficacious immunotherapies for T-ALL.

Indexed as

AnimalsCell EngineeringHumansImmunotherapy, AdoptivePrecursor T-Cell Lymphoblastic Leukemia-LymphomaReceptors, Chimeric AntigenT-LymphocytesReceptors, Chimeric Antigenchimeric antigen receptorimmunotherapyleukemia-initiating cellsmonoclonal antibodiesrelapseT-cell acute lymphoblastic leukemia

Identifiers

PMID33081391
PMCPMC7589289
OpenAlexW3093380975

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.