Evidence map›Paper›PMID 30622535›Full record

ReviewFrontiers in immunology2018

Potential Role of CXCR4 Targeting in the Context of Radiotherapy and Immunotherapy of Cancer.

Franziska Eckert, Karin Schilbach, Lukas Klumpp, Lilia Bardoscia, Efe Cumhur Sezgin, Matthias Schwab, Daniel Zips, Stephan M Huber

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing 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

76 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Blocking CXCR4Genome medicine · 2025
    Article
  6. From Hypoxia to Bone: Reprogramming the Prostate Cancer Metastatic Cascade.International journal of molecular sciences · 2025
    Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Radiosynthesis and preclinical evaluation of aEJNMMI radiopharmacy and chemistry · 2024
    Article
  14. Targeting cytokine and chemokine signaling pathways for cancer therapy.Signal transduction and targeted therapy · 2024
    Review
  15. Targeting CXCR4/CXCL12 axis via [European journal of nuclear medicine and molecular imaging · 2024
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review

16 more citing papers are in PubMed but not listed here.

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.

Franziska EckertDepartment of Radiation Oncology, University Hospital Tuebingen, Tuebingen, Germany.
Karin SchilbachDepartment of General Pediatrics/Pediatric Oncology, University Hospital Tuebingen, Tuebingen, Germany.
Lukas KlumppDepartment of Radiation Oncology, University Hospital Tuebingen, Tuebingen, Germany.
Lilia BardosciaDepartment of Radiation Oncology, University Hospital Tuebingen, Tuebingen, Germany.
Efe Cumhur SezginDepartment of Radiation Oncology, University Hospital Tuebingen, Tuebingen, Germany.
Matthias SchwabDr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology, Stuttgart, Germany.
Daniel ZipsDepartment of Radiation Oncology, University Hospital Tuebingen, Tuebingen, Germany.
Stephan M HuberDepartment of Radiation Oncology, University Hospital Tuebingen, Tuebingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer immunotherapy has been established as standard of care in different tumor entities. After the first reports on synergistic effects with radiotherapy and the induction of abscopal effects-tumor shrinkage outside the irradiated volume attributed to immunological effects of radiotherapy-several treatment combinations have been evaluated. Different immunotherapy strategies (e.g., immune checkpoint inhibition, vaccination, cytokine based therapies) have been combined with local tumor irradiation in preclinical models. Clinical trials are ongoing in different cancer entities with a broad range of immunotherapeutics and radiation schedules. SDF-1 (CXCL12)/CXCR4 signaling has been described to play a major role in tumor biology, especially in hypoxia adaptation, metastasis and migration. Local tumor irradiation is a known inducer of SDF-1 expression and release. CXCR4 also plays a major role in immunological processes. CXCR4 antagonists have been approved for the use of hematopoietic stem cell mobilization from the bone marrow. In addition, several groups reported an influence of the SDF-1/CXCR4 axis on intratumoral immune cell subsets and anti-tumor immune response. The aim of this review is to merge the knowledge on the role of SDF-1/CXCR4 in tumor biology, radiotherapy and immunotherapy of cancer and in combinatorial approaches.

Indexed as

Antineoplastic Agents, ImmunologicalBone MarrowChemokine CXCL12ChemoradiotherapyClinical Trials as TopicGene Expression Regulation, NeoplasticHematopoietic Stem Cell MobilizationHumansImmunotherapyNeoplasmsReceptors, CXCR4Signal TransductionTreatment OutcomeAntineoplastic Agents, ImmunologicalChemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanReceptors, CXCR4cancer radiotherapyCXCR4dendritic cellsimmunotherapyNK cellsregulatory T cellsSDF-1 (CXCL12)T cells

Identifiers

PMID30622535
PMCPMC6308162

What OpenQuestion holds

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LicenceCC BY
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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.