Evidence map›Paper›PMID 35740657›Full record

ReviewCancers2022

Vaccination Therapy for Acute Myeloid Leukemia: Where Do We Stand?

Kordelia Barbullushi, Nicolò Rampi, Fabio Serpenti, Mariarita Sciumè, Sonia Fabris, Pasquale De Roberto, Nicola Stefano Fracchiolla

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 25 citations in OpenAlex.

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  18. Identification of tumor antigens and immune subtypes of acute myeloid leukemia for mRNA vaccine development.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
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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

7 authors at 2 institutions in 1 country.

Kordelia BarbullushiHematology & BMT Unit, Fondazione IRCCS Ca' Granda Policlinico Ospedale Maggiore di Milano, 20122 Milan, Italy.
Nicolò RampiHematology & BMT Unit, Fondazione IRCCS Ca' Granda Policlinico Ospedale Maggiore di Milano, 20122 Milan, Italy.
Fabio SerpentiHematology & BMT Unit, Fondazione IRCCS Ca' Granda Policlinico Ospedale Maggiore di Milano, 20122 Milan, Italy.
Mariarita SciumèHematology & BMT Unit, Fondazione IRCCS Ca' Granda Policlinico Ospedale Maggiore di Milano, 20122 Milan, Italy.ORCID 0000-0001-7958-4966
Sonia FabrisHematology & BMT Unit, Fondazione IRCCS Ca' Granda Policlinico Ospedale Maggiore di Milano, 20122 Milan, Italy.
Pasquale De RobertoHematology & BMT Unit, Fondazione IRCCS Ca' Granda Policlinico Ospedale Maggiore di Milano, 20122 Milan, Italy.
Nicola Stefano FracchiollaHematology & BMT Unit, Fondazione IRCCS Ca' Granda Policlinico Ospedale Maggiore di Milano, 20122 Milan, Italy.
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy is changing the therapeutic landscape of many hematologic diseases, with immune checkpoint inhibitors, bispecific antibodies, and CAR-T therapies being its greatest expression. Unfortunately, immunotherapy in acute myeloid leukemia (AML) has given less brilliant results up to now, and the only approved drug is the antiCD33 antibody-drug conjugate gemtuzumab ozogamicin. A promising field of research in AML therapy relies on anti-leukemic vaccination to induce remission or prevent disease relapse. In this review, we analyze recent evidence on AML vaccines and their biological mechanisms. The principal proteins that have been exploited for vaccination strategies and have reached clinical experimental phases are Wilm's tumor 1, proteinase 3, and RHAMM. the majority of data deals with WT1-base vaccines, given also the high expression and mutation rates of WT1 in AML cells. Stimulators of immune responses such as TLR7 agonist and interleukin-2 have also proven anti-leukemic activity both in vivo and in vitro. Lastly, cellular vaccines mainly based on autologous or allogeneic off-the-shelf dendritic cell-based vaccines showed positive results in terms of T-cell response and safety, also in elderly patients. Compared to other immunotherapeutic strategies, anti-AML vaccines have the advantage of being a less toxic and a more manageable approach, applicable also to elderly patients with poorer performance status, and may be used in combination with currently available therapies. As for the best scenario in which to use vaccination, whether in a therapeutic, prophylactic, or preemptive setting, further studies are needed, but available evidence points to poorer results in the presence of active or high-burden disease. Given the poor prognosis of relapsed/refractory or high-risk AML, further research is urgently needed to better understand the biological pathways that sustain its pathogenesis. In this setting, research on novel frontiers of immunotherapy-based agents, among which vaccines represent important actors, is warranted to develop new and efficacious strategies to obtain long-term disease control by immune patrolling.

Indexed as

acute myeloid leukemiadendritic cellsimmunotherapyvaccination

Identifiers

PMID35740657
PMCPMC9221207
OpenAlexW4283027744

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.