Evidence map›Paper›PMID 37762763›Full record

ReviewJournal of clinical medicine2023

Harnessing Immune Response in Acute Myeloid Leukemia.

Carola Riva, Chiara Vernarecci, Paola Minetto, Rayan Goda, Marco Greppi, Silvia Pesce, Maria Chies, Giada Zecchetti, Beatrice Ferro, Elena Maio and 4 more

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
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

14 authors at 2 institutions in 1 country.

Carola RivaClinic of Hematology, Department of Internal Medicine, University of Genova, 16132 Genova, Italy.
Chiara VernarecciClinic of Hematology, Department of Internal Medicine, University of Genova, 16132 Genova, Italy.
Paola MinettoIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Rayan GodaDepartment of Experimental Medicine (DIMES), University of Genova, 16132 Genova, Italy.ORCID 0000-0003-1451-7214
Marco GreppiDepartment of Experimental Medicine (DIMES), University of Genova, 16132 Genova, Italy.
Silvia PesceDepartment of Experimental Medicine (DIMES), University of Genova, 16132 Genova, Italy.ORCID 0000-0002-9798-4944
Maria ChiesClinic of Hematology, Department of Internal Medicine, University of Genova, 16132 Genova, Italy.
Giada ZecchettiClinic of Hematology, Department of Internal Medicine, University of Genova, 16132 Genova, Italy.
Beatrice FerroClinic of Hematology, Department of Internal Medicine, University of Genova, 16132 Genova, Italy.
Elena MaioClinic of Hematology, Department of Internal Medicine, University of Genova, 16132 Genova, Italy.
Michele CeaClinic of Hematology, Department of Internal Medicine, University of Genova, 16132 Genova, Italy.ORCID 0000-0002-1530-6729
Roberto Massimo LemoliClinic of Hematology, Department of Internal Medicine, University of Genova, 16132 Genova, Italy.
Emanuela MarcenaroIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.ORCID 0000-0003-4103-7566
Fabio GuoloClinic of Hematology, Department of Internal Medicine, University of Genova, 16132 Genova, Italy.ORCID 0000-0003-3166-6078
University of Genoa · ITOspedale Policlinico San Martino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the results achieved with the evolution of conventional chemotherapy and the inclusion of targeted therapies in the treatment of acute myeloid leukemia (AML), survival is still not satisfying, in particular in the setting of relapsed/refractory (R/R) disease or elderly/unfit patients. Among the most innovative therapeutic options, cellular therapy has shown great results in different hematological malignancies such as acute lymphoblastic leukemia and lymphomas, with several products already approved for clinical use. However, despite the great interest in also expanding the application of these new treatments to R/R AML, no product has been approved yet for clinical application. Furthermore, cellular therapy could indeed represent a powerful tool and an appealing alternative to allogeneic hematopoietic stem cell transplantation for ineligible patients. In this review, we aim to provide an overview of the most recent clinical research exploring the effectiveness of cellular therapy in AML, moving from consolidated approaches such as post- transplant donor's lymphocytes infusion, to modern adoptive immunotherapies such as alloreactive NK cell infusions, engineered T and NK cells (CAR-T, CAR-NK) and novel platforms of T and NK cells engaging (i.e., BiTEs, DARTs and ANKET

Indexed as

AMLCAR-TimmunotherapyNK cells

Identifiers

PMID37762763
PMCPMC10532363
OpenAlexW4386495997

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.