Evidence map›Paper›PMID 34794794›Full record

ArticleHematology, transfusion and cell therapy2021

Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Consensus on genetically modified cells. IV: CAR-T cell therapy for multiple myeloma patients.

Angelo Maiolino, Luciano J Costa, Marcelo Pasquini, Edvan de Queiroz Crusoe, Afonso Celso Vigorito, Marco Aurélio Salvino, Fernanda Salles Seguro, Jayr Schmidt Filho, Vania Tietsche de Moraes Hungria

Open access · diamondAbstract read
In one paragraph

Article in Hematology, transfusion and cell therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. CAR T-cell therapy and the onco-nephrologist.Frontiers in nephrology · 2024
    Review
  2. Article
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

9 authors at 7 institutions in 2 countries.

Angelo MaiolinoFaculdade de Medicina, Universidade Federal do Rio de Janeiro (FM UFRJ), Rio de Janeiro, RJ, Brazil; Americas Oncologia Rio de Janeiro, Rio de Janeiro, RJ, Brazil. Electronic address: maiolino@hucff.ufrj.br.
Luciano J CostaO'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.
Marcelo PasquiniCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI, USA.
Edvan de Queiroz CrusoeComplexo Hospitalar Universitário Professor Edgard, Universidade Federal da Bahia (HUPES UFBA), Salvador, BA, Brazil; Rede D'or Oncologia, Salvador, BA, Brazil.
Afonso Celso VigoritoCentro de Hematologia e Hemoterapia da Unicamp Universidade de Campinas, Unicamp (Hemocentro Unicamp), Campinas, SP, Brazil.
Marco Aurélio SalvinoComplexo Hospitalar Universitário Professor Edgard, Universidade Federal da Bahia (HUPES UFBA), Salvador, BA, Brazil; Hospital San Rafael Rede D'or Oncologia, Salvador, BA, Brazil.
Fernanda Salles SeguroHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP), São Paulo, SP, Brazil; Instituto do Câncer do Estado de São Paulo (Icesp), São Paulo, SP, Brazil.
Jayr Schmidt FilhoAC Camargo Cancer Center, São Paulo, SP, Brazil.
Vania Tietsche de Moraes HungriaSanta Casa de Misericórdia de São Paulo, São Paulo, SP, Brazil; Clínica São Germano, São Paulo, SP, Brazil.
Universidade Federal da Bahia · BRAC Camargo Hospital · BRInstituto do Câncer do Estado de São Paulo · BRIrmandade da Santa Casa de Misericórdia de São Paulo · BRMedical College of Wisconsin · USUniversidade Federal do Rio de Janeiro · BRUniversity of Alabama at Birmingham · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extraordinary progress has been made over the last decade in the treatment of multiple myeloma with the incorporation of new drugs, particularly proteasome inhibitors, immunomodulators, and monoclonal antibodies. The combined use of innovative drugs, already in the first lines of treatment, has led to an expressive increase in the survival of these patients. However, the approach to relapse remains a great challenge, and the disease continues to be incurable. In this scenario, modern immunotherapy has gained the limelight, especially with its recent use of CAR-T cells in clinical trials, as in the case of multiple myeloma, having the BCMA as the primary target. The results are impactful in the treatment of multiple myeloma patients who have had multiple relapses and are triple- and penta-refractory. In this Consensus, we have brought together a group of experts in multiple myeloma to discuss and forward their recommendations for the future, which we hope is very near, incorporating the CAR-T in our country.

Indexed as

CAR-T cellsImmunotherapyMultiple myelomaTreatment

Identifiers

PMID34794794
PMCPMC8606706
OpenAlexW3214309981

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.