Evidence map›Paper›PMID 35467766›Full record

ArticleInternational journal of cancer2022

Genetic variation in ST6GAL1 is a determinant of capecitabine and oxaliplatin induced hand-foot syndrome.

Katie Watts, Christopher Wills, Ayman Madi, Claire Palles, Timothy S Maughan, Richard Kaplan, Nada A Al-Tassan, Rachel Kerr, David J Kerr, Richard S Houlston and 2 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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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

12 authors at 8 institutions in 2 countries.

Katie WattsDivision of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, UK.
Christopher WillsDivision of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, UK.
Ayman MadiThe Clatterbridge Cancer Centre NHS Foundation Trust, Wirral, UK.
Claire PallesInstitute of Cancer and Genomic Sciences, Institute of Biomedical Research, University of Birmingham, Birmingham, UK.
Timothy S MaughanCRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, UK.
Richard KaplanMRC Clinical Trials Unit, University College of London, London, UK.
Nada A Al-TassanDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Rachel KerrDepartment of Oncology, Old Road Campus Research Building, University of Oxford, Oxford, UK.
David J KerrNuffield Department of Clinical Laboratory Sciences, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Richard S HoulstonDivision of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
Valentina Escott-PriceInstitute of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
Jeremy P CheadleDivision of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0001-9453-8458
Cardiff University · GBUniversity of Oxford · GBCancer Research UK Clinical Trials Unit · GBClatterbridge Cancer Centre NHS Foundation Trust · GBInstitute of Cancer Research · GBJohn Radcliffe Hospital · GBKing Faisal Specialist Hospital & Research Centre · SAMRC Clinical Trials Unit at UCL · GB

Funding

Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MR/L010305/1
6 · The paper itself

Abstract

Cancer patients treated with capecitabine and oxaliplatin (XELOX) often develop hand-foot syndrome (HFS) or palmar-plantar erythrodysesthesia. Genetic variation in ST6GAL1 is a risk factor for type-2 diabetes (T2D), a disease also associated with HFS. We analysed genome-wide association data for 10 toxicities in advanced colorectal cancer (CRC) patients from the COIN and COIN-B trials. One thousand and fifty-five patients were treated with XELOX ± cetuximab and 745 with folinic acid, fluorouracil and oxaliplatin ± cetuximab. We also analysed rs6783836 in ST6GAL1 with HFS in CRC patients from QUASAR2. Using UK Biobank data, we sought to confirm an association between ST6GAL1 and T2D (17 384 cases, 317 887 controls) and analysed rs6783836 against markers of diabetes, inflammation and psoriasis. We found that 68% of patients from COIN and COIN-B with grade 2-3 HFS responded to treatment as compared to 58% with grade 0-1 HFS (odds ratio [OR] = 1.1, 95% confidence interval [CI] = 1.02-1.2, P = 2.0 × 10

Indexed as

Antigens, CDCapecitabineHand-Foot SyndromeOxaliplatinSialyltransferasesAntineoplastic Combined Chemotherapy Protocolsbeta-D-Galactoside alpha 2-6-SialyltransferaseCetuximabColorectal NeoplasmsDiabetes Mellitus, Type 2FluorouracilGenetic VariationGenome-Wide Association StudyHumansInflammationPsoriasisAntigens, CDbeta-D-Galactoside alpha 2-6-SialyltransferaseCapecitabineCetuximabFluorouracilOxaliplatinSialyltransferasesST6GAL1 protein, humanchemotherapycolorectal cancergeneticsST6GAL1toxicityXELOX

Identifiers

PMID35467766
PMCPMC9545609
OpenAlexW4224434629

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.