Evidence map›Paper›PMID 37972346›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2024

Clinical Validation of Human Papilloma Virus Circulating Tumor DNA for Early Detection of Residual Disease After Chemoradiation in Cervical Cancer.

Kathy Han, Jinfeng Zou, Zhen Zhao, Zeynep Baskurt, Yangqiao Zheng, Elizabeth Barnes, Jennifer Croke, Sarah E Ferguson, Anthony Fyles, Lilian Gien and 11 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 2 pooled it
12.7field-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

51 citing papers in PubMed, 2 syntheses or guidelines pooled it, 53 citations in OpenAlex.

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  20. Targeting innate immunity to overcome immune evasion in HPV-associated cancers.Frontiers in cellular and infection microbiology · 2026
    Review
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

21 authors at 5 institutions in 1 country.

Kathy HanPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0001-8439-3929
Jinfeng ZouPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Zhen ZhaoPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Zeynep BaskurtDepartment of Biostatistics, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0002-0714-7406
Yangqiao ZhengPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Elizabeth BarnesDepartment of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-4058-0236
Jennifer CrokePrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0002-7090-6313
Sarah E FergusonPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0002-2123-3642
Anthony FylesPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0002-3633-2483
Lilian GienOdette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.ORCID 0000-0002-6558-3337
Adam GladwishDepartment of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.
Magali Lecavalier-BarsoumJewish General Hospital, Montreal, Quebec, Canada.
Stephanie LheureuxDivision of Medical Oncology, Department of Internal Medicine, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0003-4405-5890
Jelena LukovicPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Helen MackayOdette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Eve-Lyne MarchandHopital Maisonneuve-Rosemont, Montreal, Quebec, Canada.
Ur MetserPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0003-3726-8994
Michael MilosevicPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0002-9620-6876
Amandeep S TaggarDepartment of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.
Scott V BratmanPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0001-8610-4908
Eric LeungDepartment of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.
University Health Network · CASunnybrook Health Science Centre · CAUniversity of Toronto · CAHôpital Maisonneuve-Rosemont · CAJewish General Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMost cervical cancers are caused by human papilloma virus (HPV), and HPV circulating tumor DNA (ctDNA) may identify patients at highest risk of relapse. Our pilot study using digital polymerase chain reaction (dPCR) showed that detectable HPV ctDNA at the end of chemoradiation (CRT) is associated with inferior progression-free survival (PFS) and that a next-generation sequencing approach (HPV-seq) may outperform dPCR. We aimed to prospectively validate HPV ctDNA as a tool for early detection of residual disease.

methodsThis prospective, multicenter validation study accrued patients with stage IB-IVA cervical cancer treated with CRT between 2017 and 2022. Participants underwent phlebotomy at baseline, end of CRT, 4-6 weeks post-CRT, and 3 months post-CRT for HPV ctDNA levels. Plasma HPV genotype-specific DNA levels were quantified using both dPCR and HPV-seq. The primary end point was 2-year PFS.

resultsWith a median follow-up of 2.2 (range, 0.5-5.5) years, there were 24 PFS events among the 70 patients with HPV+ cervical cancer. Patients with detectable HPV ctDNA on dPCR at the end of CRT, 4-6 weeks post-CRT, and 3 months post-CRT had significantly worse 2-year PFS compared with those with undetectable HPV ctDNA (77%

conclusionPersistent HPV ctDNA after CRT is independently associated with inferior PFS. HPV ctDNA testing can identify, as early as at the end of CRT, patients at high risk of recurrence for future treatment intensification trials.

Indexed as

Circulating Tumor DNAPapillomavirus InfectionsUterine Cervical NeoplasmsBiomarkers, TumorFemaleHuman Papillomavirus VirusesHumansNeoplasm Recurrence, LocalPilot ProjectsProspective StudiesBiomarkers, TumorCirculating Tumor DNA

Identifiers

PMID37972346
PMCPMC10824379
OpenAlexW4388724082

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.