Evidence map›Paper›PMID 36949946›Full record

ReviewFrontiers in immunology2023

Combining chemotherapy with CAR-T cell therapy in treating solid tumors.

Arthur Xuan Wang, Xiao Jing Ong, Criselle D'Souza, Paul J Neeson, Joe Jiang Zhu

Open access · goldFull text readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
17.3field-weighted citation impact, top 1% 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

60 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
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  5. Adoptive T-cell therapies in the clinic.Bioengineering & translational medicine · 2026
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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

5 authors at 2 institutions in 1 country.

Arthur Xuan WangCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Xiao Jing OngCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Criselle D'SouzaCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Paul J NeesonCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Joe Jiang ZhuCancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
The University of Melbourne · AUPeter MacCallum Cancer Centre · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapy has long been a standard treatment for a wide range of malignancies, where patients typically undergo multiple rounds of chemotherapy regimens to control tumor growth. In the clinic, the chemotherapy drugs cyclophosphamide and fludarabine are commonly used prior to Chimeric Antigen Receptor T (CAR-T) cell therapy to lymphodeplete and improve CAR-T cell engraftment. In this review, we discuss the use of chemotherapy in combination with CAR-T cell therapy. We also show that chemotherapy can deplete immunosuppressive cells, promote a pro-inflammatory tumor microenvironment, disrupt tumor stroma, and improve CAR-T cell recruitment to the tumor. Although the combination of chemotherapy plus CAR-T cell therapy is promising, certain aspects of chemotherapy also pose a challenge. In addition, the combined therapeutic effect may be heavily dependent on the dose and the treatment schedule. Thus, we also discussed the obstacles to effective clinical outcomes of the combination therapy.

Indexed as

NeoplasmsReceptors, Chimeric AntigenCell- and Tissue-Based TherapyHumansImmunotherapy, AdoptiveT-LymphocytesTumor MicroenvironmentReceptors, Chimeric AntigenchemotherapyChimeric Antigen Receptor T cell (CAR-T)personalized combinationsolid tumortumor microenvironment (TME)

Identifiers

PMID36949946
PMCPMC10026332
OpenAlexW4323318696

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read14
identifiers read11
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.