Evidence map›Paper›PMID 39195311›Full record

ArticleCurrent oncology (Toronto, Ont.)2024

Detection of HPV DNA in Saliva of Patients with HPV-Associated Oropharyngeal Cancer Treated with Radiotherapy.

Atsushi Motegi, Shun-Ichiro Kageyama, Yukie Kashima, Hidenari Hirata, Hidehiro Hojo, Masaki Nakamura, Takeshi Fujisawa, Tomohiro Enokida, Makoto Tahara, Kazuto Matsuura and 1 more

Abstract read
In one paragraph

Article in Current oncology (Toronto, Ont.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Atsushi MotegiDepartment of Radiation Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Shun-Ichiro KageyamaDepartment of Radiation Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Yukie KashimaDepartment of Translational Informatics, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Kashiwa 277-8577, Japan.
Hidenari HirataDepartment of Radiation Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Hidehiro HojoDepartment of Radiation Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Masaki NakamuraDepartment of Radiation Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.ORCID 0000-0002-4431-8892
Takeshi FujisawaDepartment of Radiation Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Tomohiro EnokidaDepartment of Head and Neck Medical Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Makoto TaharaDepartment of Head and Neck Medical Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.ORCID 0000-0001-9035-3106
Kazuto MatsuuraDepartment of Head and Neck Surgery, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Sadamoto ZendaDepartment of Radiation Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.

Funding

Japan Society for the Promotion of Science 16K10411National Cancer Center Research and Development Fund 2022-A-17
6 · The paper itself

Abstract

backgroundTo investigate the technical feasibility of RT-PCR and direct sequencing to quantify HPV DNA in the saliva of patients with Human-Papilloma-Virus related oropharyngeal cancer (HPV-OPC), the level of which is known to predict prognosis after treatment.

methodsNine patients with locally advanced HPV-OPC treated with definitive radiotherapy with chemotherapy or cetuximab, or radiotherapy alone between April 2016 and September 2017, were enrolled, two of whom also received induction chemotherapy. Saliva was collected before (baseline), during (mid-RT) and after (post-RT) radiotherapy. HPV-16 DNAs (E6 and E7) in saliva were quantified by RT-PCR and sequencing, the latter using a custom cancer panel. Correlations between HPV DNA levels and clinical outcomes were assessed.

resultsCompared to the baseline, the relative cycle threshold (Ct) value of E6 and E7 reduced at the point of mid-RT in the majority of the patients (100% and 75% for E6 and E7, respectively). Similarly, the relative Ct value from the baseline to post-RT reduced in 86% and 100% of the patients for E6 and E7, respectively. During the follow-up period, three patients (33%) experienced disease progression. The relative baseline Ct values of these three patients were in the top 4 of all the patients. The sequences of HPV DNA were detected in five (83%) of six samples of the baseline saliva that underwent DNA sequencing, along with several gene mutations, such as TP53,CDKN2A and PIK3CA.

conclusionsThis study demonstrates that, in addition to detection and quantification of HPV DNA by RT-PCR, detection by sequencing of HPV-DNA using a customized cancer panel is technically possible.

Indexed as

DNA, ViralOropharyngeal NeoplasmsPapillomavirus InfectionsSalivaAgedFemaleHuman papillomavirus 16HumansMaleMiddle AgedDNA, Viralbiomarkercancer panelchemoradiotherapyHuman-Papilloma-Virus (HPV)oropharyngeal cancer (OPC)saliva

Identifiers

PMID39195311
PMCPMC11352770

What Socratic 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 Socratic graph.