Evidence map›Paper›PMID 36805683›Full record

ArticleBMC cancer2023

Total serum N-glycans associate with response to immune checkpoint inhibition therapy and survival in patients with advanced melanoma.

Alessia Visconti, Niccolò Rossi, Helena Deriš, Karla A Lee, Maja Hanić, Irena Trbojević-Akmačić, Andrew M Thomas, Laura A Bolte, Johannes R Björk, Jahlisa S Hooiveld-Noeken and 17 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.1field-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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
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

27 authors at 11 institutions in 5 countries.

Alessia ViscontiDepartment of Twins Research & Genetics Epidemiology, King's College London, London, UK.
Niccolò RossiDepartment of Twins Research & Genetics Epidemiology, King's College London, London, UK.
Helena DerišGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Karla A LeeDepartment of Twins Research & Genetics Epidemiology, King's College London, London, UK.
Maja HanićGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Irena Trbojević-AkmačićGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Andrew M ThomasCIBIO, University of Trento, Trento, Italy.
Laura A BolteDepartment of Gastroenterology and Hepatology, University of Groningen and University Medical Center, Groningen, The Netherlands.
Johannes R BjörkDepartment of Gastroenterology and Hepatology, University of Groningen and University Medical Center, Groningen, The Netherlands.
Jahlisa S Hooiveld-NoekenDepartment of Medical Oncology, University Medical Center Groningen, Groningen, The Netherlands.
Ruth BoardDepartment of Oncology, Lancashire Teaching Hospitals NHS Trust, Chorley, UK.
Mark HarlandDivision of Haematology and Immunology, Institute of Medical Research at St. James', University of Leeds, Leeds, UK.
Julia Newton-BishopDivision of Haematology and Immunology, Institute of Medical Research at St. James', University of Leeds, Leeds, UK.
Mark HarriesDepartment of Medical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Joseph J SaccoLiverpool Clatterbridge Cancer Centre, Liverpool, UK.
Paul LoriganThe Christie NHS Foundation Trust, Manchester, UK.
Heather M ShawDepartment of Medical Oncology, Mount Vernon Cancer Centre, Northwood, UK.
Elisabeth G E de VriesDepartment of Medical Oncology, University Medical Center Groningen, Groningen, The Netherlands.
Rudolf S N FehrmannDepartment of Medical Oncology, University Medical Center Groningen, Groningen, The Netherlands.
Rinse K WeersmaDepartment of Gastroenterology and Hepatology, University of Groningen and University Medical Center, Groningen, The Netherlands.
Tim D SpectorDepartment of Twins Research & Genetics Epidemiology, King's College London, London, UK.
Paul NathanDepartment of Medical Oncology, Mount Vernon Cancer Centre, Northwood, UK.
Geke A P HospersDepartment of Medical Oncology, University Medical Center Groningen, Groningen, The Netherlands.
Peter SasieniSchool of Cancer and Pharmaceutical Sciences, King's College London, London, UK.
Veronique Bataille *Department of Twins Research & Genetics Epidemiology, King's College London, London, UK. bataille@doctors.org.uk.ORCID http://orcid.org/0000-0002-8750-4150
Gordan Lauc *Genos Glycoscience Research Laboratory, Zagreb, Croatia.
Mario Falchi *Department of Twins Research & Genetics Epidemiology, King's College London, London, UK. mario.falchi@kcl.ac.uk.ORCID http://orcid.org/0000-0002-5646-1004
King's College London · GBUniversity Medical Center Groningen · NLGenos (Croatia) · HRMount Vernon Cancer Centre · GBUniversity of Leeds · GBGuy's and St Thomas' NHS Foundation Trust · GBLancashire Teaching Hospitals NHS Foundation Trust · GBThe Christie NHS Foundation Trust · GBUniversity of Liverpool · GBUniversity of Trento · ITUniversity of Zagreb · HR

Funding

Cancer Research UK 25356Cancer Research UK 27047Medical Research Council MR/MO19012/1
6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) have revolutionized the treatment of melanoma and other cancers. However, no reliable biomarker of survival or response has entered the clinic to identify those patients with melanoma who are most likely to benefit from ICIs. Glycosylation affects proteins and lipids' structure and functions. Tumours are characterized by aberrant glycosylation which may contribute to their progression and hinder an effective antitumour immune response.

methodsWe aim at identifying novel glyco-markers of response and survival by leveraging the N-glycome of total serum proteins collected in 88 ICI-naive patients with advanced melanoma from two European countries. Samples were collected before and during ICI treatment.

resultsWe observe that responders to ICIs present with a pre-treatment N-glycome profile significantly shifted towards higher abundancy of low-branched structures containing lower abundances of antennary fucose, and that this profile is positively associated with survival and a better predictor of response than clinical variables alone.

conclusionWhile changes in serum protein glycosylation have been previously implicated in a pro-metastatic melanoma behaviour, we show here that they are also associated with response to ICI, opening new avenues for the stratification of patients and the design of adjunct therapies aiming at improving immune response.

Indexed as

Immune Checkpoint InhibitorsMelanomaAmbulatory Care FacilitiesEuropeHumansPolysaccharidesImmune Checkpoint InhibitorsPolysaccharidesImmune checkpoint inhibitorsMelanomaResponseSurvivalTotal serum N-glycomics

Identifiers

PMID36805683
PMCPMC9938582
OpenAlexW4321329184

What OpenQuestion holds

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Registered trials

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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.