Evidence map›Paper›PMID 33882636›Full record

ReviewHaematologica2021

Targeting the tumor microenvironment in chronic lymphocytic leukemia.

Rebecka Svanberg, Sine Janum, Piers E M Patten, Alan G Ramsay, Carsten U Niemann

Open access · goldAbstract readReview
In one paragraph

Review in Haematologica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

57 citing papers in PubMed, 84 citations in OpenAlex.

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  14. Disruption of constitutive CXCR4 oligomers impairs oncogenic properties in lymphoid neoplasms.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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 2 countries.

Rebecka SvanbergDepartment of Hematology, Rigshospitalet, Copenhagen.
Sine JanumDepartment of Clinical Haemato-oncology, Bartholomew's Hospital, Barts Health Trust, London.
Piers E M PattenSchool of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London.
Alan G RamsaySchool of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London.
Carsten U NiemannDepartment of Hematology, Rigshospitalet, Copenhagen. carsten.utoft.niemann@regionh.dk.
King's College London · GBRigshospitalet · DK

Funding

Medical Research Council MR/T005106/1
6 · The paper itself

Abstract

The tumor microenvironment (TME) plays an essential role in the development, growth, and survival of the malignant B-cell clone in chronic lymphocytic leukemia (CLL). Within the proliferation niches of lymph nodes, bone marrow, and secondary lymphoid organs, a variety of phenotypically and functionally altered cell types, including T cells, natural killer cells, monocytes/macrophages, endothelial and mesenchymal stroma cells, provide crucial survival signals, along with CLL-cellinduced suppression of antitumor immune responses. The B-cell receptor pathway plays a pivotal role in mediating the interaction between CLL cells and the TME. However, an increasing number of additional components of the multifactorial TME are being discovered. Although the majority of therapeutic strategies employed in CLL hitherto have focused on targeting the leukemic cells, emerging evidence implies that modulation of microenvironmental cells and CLL-TME interactions by novel therapeutic agents significantly affect their clinical efficacy. Thus, improving our understanding of CLL-TME interactions and how they are affected by current therapeutic agents may improve and guide treatment strategies. Identification of novel TME interactions may also pave the road for the development of novel therapeutic strategies targeting the TME. In this review, we summarize current evidence on the effects of therapeutic agents on cells and interactions within the TME. With a growing demand for improved and personalized treatment options in CLL, this review aims at inspiring future exploration of smart drug combination strategies, translational studies, and novel therapeutic targets in clinical trials.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellBone MarrowHumansReceptors, Antigen, B-CellT-LymphocytesTumor MicroenvironmentReceptors, Antigen, B-Cell

Identifiers

PMID33882636
PMCPMC8409023
OpenAlexW3154374554

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.