Evidence map›Paper›PMID 36900167›Full record

ArticleCancers2023

Methylated Cell-Free DNA Sequencing (MeD-seq) of LpnPI Digested Fragments to Identify Early Progression in Metastatic Renal Cell Carcinoma Patients on Watchful Waiting.

Manouk K Bos, Sarah R Verhoeff, Sjoukje F Oosting, Willemien C Menke-van der Houven van Oordt, Ruben G Boers, Joachim B Boers, Joost Gribnau, John W M Martens, Stefan Sleijfer, Carla M L van Herpen and 1 more

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In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

11 authors.

Manouk K BosDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0002-2984-7542
Sarah R VerhoeffDepartment of Medical Oncology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Sjoukje F OostingDepartment of Medical Oncology, University Medical Centre Groningen, 9713 GZ Groningen, The Netherlands.
Willemien C Menke-van der Houven van OordtDepartment of Medical Oncology, Cancer Center Amsterdam, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HZ Amsterdam, The Netherlands.
Ruben G BoersDepartment of Developmental Biology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0002-3377-2897
Joachim B BoersDepartment of Developmental Biology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
Joost GribnauDepartment of Developmental Biology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
John W M MartensDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0002-3428-3366
Stefan SleijferDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, 3015 GD Rotterdam, The Netherlands.
Carla M L van HerpenDepartment of Medical Oncology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Saskia M WiltingDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0002-2838-841X

Funding

Dutch Cancer Society Alpe d'HuZes Grant RUG 2012-290 5400Dutch Cancer Society no. NKB-EMCR-2016-108154
6 · The paper itself

Abstract

According to the current guidelines, watchful waiting (WW) is a feasible option for patients with good or intermediate prognosis renal-cell carcinoma (RCC). However, some patients rapidly progress during WW, requiring the initiation of treatment. Here, we explore whether we can identify those patients using circulating cell-free DNA (cfDNA) methylation. We first defined a panel of RCC-specific circulating methylation markers by intersecting differentially methylated regions from a publicly available dataset with known RCC methylation markers from the literature. The resulting RCC-specific methylation marker panel of 22 markers was subsequently evaluated for an association with rapid progression by methylated DNA sequencing (MeD-seq) in serum from 10 HBDs and 34 RCC patients with a good or intermediate prognosis starting WW in the IMPACT-RCC study. Patients with an elevated RCC-specific methylation score compared to HBDs had a shorter progression-free survival (PFS,

Indexed as

cfDNADNA methylationmetastatic renal cell carcinomawatchful waiting

Identifiers

PMID36900167
PMCPMC10000042

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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.