Evidence map›Paper›PMID 40089746›Full record

ReviewJournal of experimental & clinical cancer research : CR2025

Are monocytes a preferable option to develop myeloid cell-based therapies for solid tumors?

Daisy Bhatia, Riccardo Dolcetti, Roberta Mazzieri

Abstract readReview
In one paragraph

Review in Journal of experimental & clinical cancer research : CR, 2025. 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
–field-weighted citation impact
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.

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

3 authors.

Daisy Bhatia *Swiss Federal Institute of Technology, Lausanne, Switzerland.
Riccardo Dolcetti *Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia. Riccardo.Dolcetti@petermac.org.
Roberta Mazzieri *Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia. Roberta.Mazzieri@petermac.org.

Funding

National Breast Cancer Foundation IIRS-20-124National Health and Medical Research Council 2038700
6 · The paper itself

Abstract

In the last two decades, novel and promising cell-based therapies have populated the treatment landscape for haematological tumors. However, commonly exploited T and NK cell-based therapies show limited applicability to solid tumors. This is mainly given by the impaired tumor trafficking capability and limited effector activity of these cells within a highly immunosuppressive tumor microenvironment. Myeloid cells spontaneously home to tumors and can thus be reprogrammed and/or engineered to directly attack tumor cells or locally and selectively deliver therapeutically relevant payloads that may improve the efficacy of immunotherapy against difficult-to-access solid tumors. In the context of myeloid cell-based therapies, adoptive transfer of monocytes has often been overshadowed by infusion of differentiated macrophages or hematopoietic stem cell transplantation despite their promising therapeutic potential. Here, we summarize the recent improvements and benefits of using monocytes for the treatment of solid tumors, their current clinical applications and the challenges of their use as well as some possible strategies to overcome them.

Indexed as

Cell- and Tissue-Based TherapyMonocytesMyeloid CellsNeoplasmsAnimalsHumansImmunotherapyTumor MicroenvironmentAdoptive cell therapyChimeric antigen receptorsImmunotherapyMacrophagesMonocytes

Identifiers

PMID40089746
PMCPMC11909881

What OpenQuestion holds

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Registered trials

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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.