Evidence map›Paper›PMID 36323430›Full record

ArticleJournal for immunotherapy of cancer2022

Immune-based biomarker accurately predicts response to imiquimod immunotherapy in cervical high-grade squamous intraepithelial lesions.

Ziena Abdulrahman, Natasja Hendriks, Arnold J Kruse, Antonios Somarakis, Anna J M van de Sande, Heleen J van Beekhuizen, Jurgen M J Piek, Noel F C C de Miranda, Loes F S Kooreman, Brigitte F M Slangen and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 12 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

13 authors at 4 institutions in 1 country.

Ziena AbdulrahmanLeiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-9079-0293
Natasja HendriksMaastricht University Medical Centre+, Maastricht, The Netherlands.
Arnold J KruseMaastricht University Medical Centre+, Maastricht, The Netherlands.
Antonios SomarakisLeiden University Medical Center, Leiden, The Netherlands.
Anna J M van de SandeErasmus Medical Center, Rotterdam, The Netherlands.
Heleen J van BeekhuizenErasmus Medical Center, Rotterdam, The Netherlands.
Jurgen M J PiekCatharina Hospital, Eindhoven, The Netherlands.
Noel F C C de MirandaLeiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-6122-1024
Loes F S KooremanMaastricht University Medical Centre+, Maastricht, The Netherlands.
Brigitte F M SlangenMaastricht University Medical Centre+, Maastricht, The Netherlands.
Sjoerd H van der Burg *Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-6556-0354
Peggy J de Vos van Steenwijk *Maastricht University Medical Centre+, Maastricht, The Netherlands.
Edith M G van Esch *Catharina Hospital, Eindhoven, The Netherlands edith.v.esch@catharinaziekenhuis.nl.
Maastricht University Medical Centre · NLLeiden University Medical Center · NLErasmus MC · NLRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe complete response rate of cervical high-grade squamous intraepithelial lesion (cHSIL) patients to imiquimod immunotherapy is approximately 60%. Consequently, many patients are exposed to unnecessary adverse effects of imiquimod. On the other hand, conventional surgical large loop excision therapy is associated with increased risk of premature births in subsequent pregnancies. An in-depth analysis of the cHSIL immune microenvironment was performed in order to identify and develop a predictive biomarker for response to imiquimod, to maximize therapy efficacy and to avoid adverse effects in patients unlikely to respond.

methodsBiopsies of 35 cHSIL patients, before and 10 weeks on imiquimod treatment, were analyzed by two multispectral seven-color immunofluorescence panels for T cell and myeloid cell composition in relation to treatment response. Based on these results a simplified immunohistochemical detection protocol was developed. Samples were scanned with the Vectra multispectral imaging system and cells were automatically identified using machine learning.

resultsThe immune microenvironment of complete responders (CR) is characterized by a strong and coordinated infiltration by T helper cells (activated PD1

conclusionThe capacity of cHSIL patients to respond to imiquimod is associated with a pre-existing coordinated local immune process, fostering an imiquimod-mediated increase in local T cell infiltration. The CIBI immunohistochemical biomarker has strong potential to select cHSIL patients with a high likelihood to experience a complete response to imiquimod immunotherapy.

Indexed as

Carcinoma in SituCarcinoma, Squamous CellSquamous Intraepithelial LesionsAminoquinolinesBiomarkersHumansImiquimodImmunologic FactorsImmunotherapyTumor MicroenvironmentAminoquinolinesBiomarkersImiquimodImmunologic Factorsbiomarkers, tumorimmunotherapytumor microenvironment

Identifiers

PMID36323430
PMCPMC9639137
OpenAlexW4307988431

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.