Evidence map›Paper›PMID 34053179›Full record

SynthesisClinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery2021

The immunotherapeutic role of indoleamine 2,3-dioxygenase in head and neck squamous cell carcinoma: A systematic review.

Daniel J Lin, James C K Ng, Lei Huang, Max Robinson, James O'Hara, Janet A Wilson, Andrew L Mellor

Open access · hybridAbstract readSystematic Review
In one paragraph

Synthesis in Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. The immunotherapeutic role of indoleamine 2,3-dioxygenase in head and neck squamous cell carcinoma: A systematic review.Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery · 2021
    Pooled it
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  9. Microenvironment-based immunotherapy in oral cancer: a comprehensive review.Medical oncology (Northwood, London, England) · 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

7 authors at 2 institutions in 1 country.

Daniel J LinTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0002-0890-0148
James C K NgENT Department, Freeman Hospital, High Heaton, Newcastle upon Tyne, UK.
Lei HuangTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Max RobinsonCentre for Oral Health Research, Newcastle University, Newcastle upon Tyne, UK.
James O'HaraENT Department, Freeman Hospital, High Heaton, Newcastle upon Tyne, UK.
Janet A WilsonENT Department, Freeman Hospital, High Heaton, Newcastle upon Tyne, UK.
Andrew L MellorTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Freeman Hospital · GBNewcastle University · GB

Funding

Medical Research Council MR/N005872/1Oracle Cancer Trust BH192138Royal College of Surgeons of Edinburgh BH181442Royal College of Surgeons of England BH180499Wellcome TrustWellcome Trust BH182291
6 · The paper itself

Abstract

backgroundNovel cancer immunotherapy seeks to harness the body's own immune system and tip the balance in favour of antitumour activity. The intracellular enzyme indoleamine 2,3-dioxygenase (IDO) is a critical regulator of the tumour microenvironment (TME) via tryptophan metabolism. The potential immunotherapeutic role of IDO in head and neck squamous cell carcinoma (HNSCC) requires further exploration. We aim to assess the evidence on IDO in HNSCC.

methodsA systematic review of literature and clinical trials databases.

resultsWe included 40 studies: seven involved cell lines: eight assessed tumour immunohistochemistry: ten measured IDO gene transcription: 15 reported on clinical trials. Increased cell line IDO expression was postulated to adversely affect tumour metabolism and apoptosis. Immunohistochemical IDO expression correlated with worse survival. Gene transcription studies associated IDO with positive PD-L1 and human papillomavirus (HPV) status. Phase I/II clinical trials showed (a) overall response (34%-55%) and disease control rates (62%-70%) for IDO1 inhibitor in combination with a PD-1 inhibitor, (b) similar safety profiles when both are used in combination therapy compared to each as monotherapies and (c) IDO gene expression as a predictive biomarker for response to PD-L1 therapy.

conclusionsIDO expression is increased in the TME of HNSCC, which correlates with poor prognosis. However, the exact mechanism of IDO-driven immune modulation in the TME is an enigma. Future translational studies should map IDO activity during HNSCC treatment and elucidate its precise role in the TME, such research will underpin the development of clinical trials establishing the efficacy of IDO inhibitors in HNSCC.

Indexed as

Biomarkers, TumorCell Line, TumorHumansImmunotherapyIndoleamine-Pyrrole 2,3,-DioxygenaseSquamous Cell Carcinoma of Head and NeckTumor MicroenvironmentBiomarkers, TumorIndoleamine-Pyrrole 2,3,-Dioxygenasebiomarkersimmune systemimmunotherapyindoleamine-pyrrole 2,3-dioxygenasesquamous cell carcinoma of head and necktryptophantumour microenvironment

Identifiers

PMID34053179
PMCPMC8600953
OpenAlexW3164178299

What OpenQuestion holds

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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.