Evidence map›Paper›PMID 34022731›Full record

ArticleESMO open2021

HPV ctDNA detection of high-risk HPV types during chemoradiotherapy for locally advanced cervical cancer.

L Cabel, C Bonneau, A Bernard-Tessier, D Héquet, C Tran-Perennou, G Bataillon, R Rouzier, J-G Féron, V Fourchotte, J-F Le Brun and 10 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in ESMO open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 41 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 3 pooled it
4.5field-weighted citation impact, top 4% 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.

NCT06640283 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

Dynamic Assessment of ctDNA in Patients With Cervical and Anal Canal Tumors to Optimize Follow-up and Clinical Outcomes in the Brazilian Unified Health System (SUS)

TypeinterventionalSponsorInstituto do Cancer do Estado de São PauloRan2025 to 2027Enrolled150ConditionsHPV-Related Carcinoma, Uterine Cervical Cancer, Anal Canal Cancer, HPV-Related Anal Squamous Cell CarcinomaArmsctDNA test, Pembrolizumab
NCT07673211 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

A Prognostic Research on First-Line Recurrent and Metastatic Cervical Cancer Using Circulating Cell-Free DNA and Human Papillomavirus Detection

Typeobservational_patient_registrySponsorZhejiang Cancer HospitalRan2026 to 2029Enrolled60ConditionsCervical Cancer, Recurrent Cervical Cancer, Metastatic Cervical CancerArmsBiospecimen collection (peripheral blood and paraffin tumor tissue)
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 3 syntheses or guidelines pooled it, 73 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

20 authors at 6 institutions in 1 country.

L CabelDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, France.
C BonneauUVSQ, Paris-Saclay University, Gif-sur-Yvette, France; Department of Surgical Oncology, Institut Curie, Saint Cloud, France.
A Bernard-TessierDepartment of Pathology and Genetics, Institut Curie, Paris and Saint Cloud, France.
D HéquetDepartment of Surgical Oncology, Institut Curie, Saint Cloud, France; U900, UVSQ, Paris-Saclay University, Gif-sur-Yvette, France.
C Tran-PerennouDepartment of Pathology and Genetics, Institut Curie, Paris and Saint Cloud, France.
G BataillonDepartment of Pathology and Genetics, Institut Curie, Paris and Saint Cloud, France.
R RouzierDepartment of Surgical Oncology, Institut Curie, Saint Cloud, France; U900, UVSQ, Paris-Saclay University, Gif-sur-Yvette, France.
J-G FéronDepartment of Surgical Oncology, Institut Curie, Saint Cloud, France.
V FourchotteDepartment of Surgical Oncology, Institut Curie, Saint Cloud, France.
J-F Le BrunDepartment of Gynecology and Obstetrics, CCC François Baclesse, Caen, France.
C BenoîtDepartment of Radiation Oncology, Centre Jean Perrin, Clermont-Ferrand, France.
M RodriguesDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, France.
N ScherDepartment of Radiation Oncology, Institut Curie, Paris and Saint Cloud, France.
M MinsatDepartment of Radiation Oncology, Institut Curie, Paris and Saint Cloud, France.
M-E LegrierDepartment of Research, Institut Curie, Paris and Saint Cloud, France.
I BiècheDepartment of Pathology and Genetics, Institut Curie, Paris and Saint Cloud, France; Paris University, Paris, France.
C ProudhonCirculating Tumor Biomarkers Laboratory, Institut Curie, Paris, France.
X Sastre-GarauDepartment of Pathology, Hôpital Intercommunal de Créteil, Créteil, France.
F-C BidardDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, France; UVSQ, Paris-Saclay University, Gif-sur-Yvette, France; Circulating Tumor Biomarkers Laboratory, Institut Curie, Paris, France.
E JeannotDepartment of Pathology and Genetics, Institut Curie, Paris and Saint Cloud, France. Electronic address: emmanuelle.jeannot@curie.fr.
Institut Curie · FRCentre François Baclesse · FRCentre Jean Perrin · FRHôpital Intercommunal de Créteil · FRUniversité de Versailles Saint-Quentin-en-Yvelines · FRUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChemoradiotherapy (CRT) is the standard of care for patients diagnosed with locally advanced cervical cancer (LACC), a human papillomavirus (HPV)-related cancer that relapses in 30%-60% of patients. This study aimed to (i) design HPV droplet digital PCR (ddPCR) assays for blood detection (including rare genotypes) and (ii) monitor blood HPV circulating tumor DNA (HPV ctDNA) levels during CRT in patients with LACC.

methodsWe analyzed blood and tumor samples from 55 patients with HPV-positive LACC treated by CRT in a retrospective cohort (n = 41) and a prospective cohort (n = 14). HPV-ctDNA detection was carried out by genotype-specific ddPCR.

resultsHPV ctDNA was successfully detected in 69% of patients (n = 38/55) before CRT for LACC, including nine patients with a rare genotype. HPV-ctDNA level was correlated with HPV copy number in the tumor (r = 0.41, P < 0.001). HPV-ctDNA positivity for HPV18 (20%, n = 2/10) was significantly lower than for HPV16 (77%, n = 27/35) or other types (90%, n = 9/10, P = 0.002). HPV-ctDNA detection (positive versus negative) before CRT was associated with tumor stage (P = 0.037) and lymph node status (P = 0.02). Taking into account all samples from the end of CRT and during follow-up in the prospective cohort, positive HPV-ctDNA detection was associated with lower disease-free survival (DFS) (P = 0.048) and overall survival (OS) (P = 0.0013).

conclusionThis is one of the largest studies to report HPV-ctDNA detection before CRT and showed clearance of HPV ctDNA at the end of treatment in most patients. Residual HPV ctDNA at the end of CRT or during follow-up could help to identify patients more likely to experience subsequent relapse.

Indexed as

AlphapapillomavirusCirculating Tumor DNAPapillomavirus InfectionsUterine Cervical NeoplasmsChemoradiotherapyFemaleHumansNeoplasm Recurrence, LocalPapillomaviridaeProspective StudiesRetrospective StudiesCirculating Tumor DNAcervical cancerchemoradiotherapycirculating tumor DNAhuman papillomavirusprognostic marker

Identifiers

PMID34022731
PMCPMC8164037
OpenAlexW3160047593

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

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.