Evidence map›Paper›PMID 27884973›Full record

ReviewHaematologica2017

The emerging role of immune checkpoint inhibition in malignant lymphoma.

Ida Hude, Stephanie Sasse, Andreas Engert, Paul J Bröckelmann

Open access · goldAbstract readReview
In one paragraph

Review in Haematologica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
9.5field-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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 111 citations in OpenAlex.

  1. Guideline
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  10. Increasing Role of Targeted Immunotherapies in the Treatment of AML.International journal of molecular sciences · 2022
    Review
  11. Identification ofFrontiers in genetics · 2022
    Article
  12. Article
  13. Review
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  15. PDCD1 and IFNL4 genetic variants and risk of developing hepatitis C virus-related diseases.Liver international : official journal of the International Association for the Study of the Liver · 2021
    Article
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  17. Review
  18. Review
  19. 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

4 authors at 2 institutions in 2 countries.

Ida HudeDepartment of Internal Medicine, Division of Hematology, University Hospital Center Zagreb, Croatia.
Stephanie SasseDepartment I of Internal Medicine and German Hodgkin Study Group (GHSG), University Hospital of Cologne, Germany.
Andreas EngertDepartment I of Internal Medicine and German Hodgkin Study Group (GHSG), University Hospital of Cologne, Germany.
Paul J BröckelmannDepartment I of Internal Medicine and German Hodgkin Study Group (GHSG), University Hospital of Cologne, Germany paul.broeckelmann@uk-koeln.de.
University Hospital Cologne · DEUniversity Hospital Centre Zagreb · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To evade elimination by the host immune system, tumor cells commonly exploit physiological immune checkpoint pathways, restraining efficient anti-tumor immune cell function. Growing understanding of the complex dialog between tumor cells and their microenvironment contributed to the development of immune checkpoint inhibitors. This innovative strategy has demonstrated paradigm-shifting clinical activity in various malignancies. Antibodies targeting programmed death 1 and cytotoxic T-lymphocyte-associated protein-4 are also being investigated in lymphoid malignancies with varying levels of activity and a favorable toxicity profile. To date, evaluated only in the setting of relapsed or refractory disease, anti-programmed death 1 antibodies such as nivolumab and pembrolizumab show encouraging response rates particularly in classical Hodgkin lymphoma but also in follicular lymphoma and diffuse-large B-cell lymphoma. As the first immune checkpoint inhibitor in lymphoma, nivolumab was approved for the treatment of relapsed or refractory classical Hodgkin lymphoma by the Food and Drug Administration in May 2016. In this review, we assess the role of the pathways involved and potential rationale of checkpoint inhibition in various lymphoid malignancies. In addition to data from current clinical trials, immune-related side effects, potential limitations and future perspectives including promising combinatory approaches with immune checkpoint inhibition are discussed.

Indexed as

Molecular Targeted TherapyAntibodies, MonoclonalAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenBiomarkers, TumorCombined Modality TherapyCTLA-4 AntigenHumansImmunomodulationLymphomaProgrammed Cell Death 1 ReceptorSignal TransductionT-Lymphocyte SubsetsTreatment OutcomeAntibodies, MonoclonalAntineoplastic AgentsB7-H1 AntigenBiomarkers, TumorCTLA-4 AntigenProgrammed Cell Death 1 Receptor

Identifiers

PMID27884973
PMCPMC5210230
OpenAlexW2552978108

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.