ArticleNPJ precision oncology2026
The clinical application value of dynamic monitoring of HPV ctDNA in concurrent chemoradiotherapy for locally advanced cervical cancer.
Article in NPJ precision oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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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.
The trial behind it
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Who cites it
4 citing papers in PubMed.
- Liquid Biopsy for Minimal Residual Disease Assessment in Endometrial and Cervical Cancers: Molecular Rationale, Clinical Evidence, and Translational Barriers.International journal of molecular sciences · 2026Review
- Survival outcomes of low-dose and high-dose bevacizumab front-line maintenance in advanced high-grade serous ovarian cancer: a propensity score-matched real-world study.Frontiers in oncology · 2026Article
- DDOST mediates cervical cancer cell malignant progression by interacting with SMARCA4.American journal of cancer research · 2026Article
- Immune remodeling during cervical cancer chemoradiotherapy: temporal biomarkers and the timing of checkpoint blockade.Frontiers in immunology · 2026Review
Corrections and comments
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The treatment principle for locally advanced cervical cancer is concurrent chemoradiotherapy (CCRT). However, local recurrence or distant metastasis may still occur after the completion of CCRT. Currently, there is no effective method to monitor the efficacy of CCRT and predict prognosis. This study aims to predict the therapeutic efficacy and prognosis by dynamically monitoring human papillomavirus (HPV) circulating tumor DNA (HPV ctDNA) levels. We enrolled 31 patients with locally advanced cervical cancer and used the HPV-Seq (14 subtypes) to quantify HPV genotype-specific DNA in plasma and tissues before and during CCRT, and in the post-treatment plasma. Regular imaging was performed to evaluate tumor regression. HPV reads in plasma and tissues decreased significantly during treatment (p < 0.05). Higher HPV ctDNA levels were associated with poorer treatment outcomes (p < 0.05). In univariate and multivariate analyzes, dynamic changes in plasma HPV ctDNA were an independent factor for predicting early treatment outcome. These findings indicate that longitudinal HPV ctDNA monitoring reflects the efficacy of CCRT in locally advanced cervical cancer and provides a basis for earlier identification of candidates for post-CCRT treatment intensive and prognostic stratification.
Identifiers
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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.