Evidence map›Paper›PMID 25724841›Full record

ArticleCancer immunology, immunotherapy : CII2015

Preclinical activity of anti-CCR7 immunotherapy in patients with high-risk chronic lymphocytic leukemia.

Carlos Cuesta-Mateos, Javier Loscertales, Anna Kreutzman, Beatriz Colom-Fernández, Itxaso Portero-Sáinz, Juan José Pérez-Villar, Fernando Terrón, Cecilia Muñoz-Calleja

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. A novel anti-mouse CCR7 monoclonal antibody, CBiochemistry and biophysics reports · 2025
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  5. Article
  6. Review
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  11. C-C motif chemokine receptors in gastric cancer.Molecular and clinical oncology · 2018
    Article
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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

8 authors at 1 institution in 1 country.

Carlos Cuesta-MateosServicio de Inmunología, Departamento de Inmunología, Instituto de Investigación Sanitaria Hospital Universitario de La Princesa, C/Diego de León 62, 28006, Madrid, Spain, carlos.cuesta@salud.madrid.org.
Javier Loscertales
Anna Kreutzman
Beatriz Colom-Fernández
Itxaso Portero-Sáinz
Juan José Pérez-Villar
Fernando Terrón
Cecilia Muñoz-Calleja
Hospital Universitario de La Princesa · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic lymphocytic leukemia (CLL) with deletions of the p53 locus on chromosome 17 and/or refractory to fludarabine chemoimmunotherapy remains a major clinical problem with few therapeutic options. Currently, these types of CLL are treated with approaches that do not target the p53 pathway, such as small molecules and monoclonal antibodies (mAb). We have previously postulated anti-CCR7 mAb therapy as a novel CLL treatment. In the present study, we evaluated the in vitro efficacy of anti-CCR7 mAb as a single agent in CLL patients with high-risk cytogenetics and/or refractory to fludarabine, by measuring CCR7 surface expression and complement-dependent cytotoxicity. Our results demonstrate that CCR7 is highly expressed in challenging and heavily treated CLL patients. In addition, the complement-mediated mechanism of action of this mAb effectively eradicates CLL cells while sparing subsets of T cells in these patients. Moreover, this mAb outperformed the activity of alemtuzumab, the mAb with the highest efficacy in these groups. Finally, in vitro activity was also demonstrated in patients with a disease refractory to both fludarabine and alemtuzumab, and patients harboring 11q22 deletion. Our results propose that anti-CCR7 mAb is an effective and promising future treatment in high-risk CLL.

Indexed as

AlemtuzumabAntibodies, Monoclonal, HumanizedAntibodies, Monoclonal, Murine-DerivedGenes, p53HumansImmunophenotypingImmunotherapyLeukemia, Lymphocytic, Chronic, B-CellReceptors, CCR7Risk FactorsAlemtuzumabAntibodies, Monoclonal, HumanizedAntibodies, Monoclonal, Murine-DerivedCCR7 protein, humanReceptors, CCR7

Identifiers

PMID25724841
PMCPMC11029146
OpenAlexW2117173232

What OpenQuestion holds

Textmetadata
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.