Evidence map›Paper›PMID 38580393›Full record

ArticleLife science alliance2024

Sensitive circulating tumor DNA-based residual disease detection in epithelial ovarian cancer.

Heini Ml Kallio, Kalle Savolainen, Tuomo Virtanen, Lauri Ryyppö, Hanna Selin, Päivi Martikainen, Synnöve Staff, Kati Kivinummi, Joonatan Sipola, Juuso Vuorinen and 4 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 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

14 authors at 2 institutions in 1 country.

Heini Ml KallioFaculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere, Finland.ORCID 0000-0003-4345-1787
Kalle SavolainenDepartment of Obstetrics and Gynecology, Tays Cancer Centre, Tampere University Hospital, Tampere, Finland.ORCID 0000-0002-1244-7200
Tuomo VirtanenFaculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere, Finland.
Lauri RyyppöFaculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere, Finland.
Hanna SelinFaculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere, Finland.
Päivi MartikainenFaculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere, Finland.
Synnöve StaffDepartment of Obstetrics and Gynecology, Tays Cancer Centre, Tampere University Hospital, Tampere, Finland.
Kati KivinummiFaculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere, Finland.ORCID 0000-0002-5788-835X
Joonatan SipolaFaculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere, Finland.
Juuso VuorinenFaculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere, Finland.
Jussi NikkolaDepartment of Urology, Tampere University Hospital, Tampere, Finland.ORCID 0000-0002-5077-2012
Matti NykterFaculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere, Finland.
Annika AuranenDepartment of Obstetrics and Gynecology, Tays Cancer Centre, Tampere University Hospital, Tampere, Finland annika.auranen@pirha.fi.ORCID 0000-0002-9678-4684
Matti AnnalaFaculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere, Finland matti.annala@tuni.fi.ORCID 0000-0001-8478-9026
Tampere University · FITampere University Hospital · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelial ovarian cancer (EOC) is one of the leading causes of cancer-related death in women worldwide, and is characterized by a high rate of recurrence after surgery and chemotherapy. We sought to implement a circulating tumor DNA (ctDNA)-based blood test for more accurate post-operative surveillance of this disease. We analyzed 264 plasma samples collected between June 2016 and September 2021 from 63 EOC patients using tumor-guided plasma cell-free DNA analysis to detect residual disease after treatment. Assay specificity was verified using cross-patient analysis of 1,195 control samples. ctDNA was detected in 51 of 55 (93%) samples at diagnosis, and 18 of 18 (100%) samples at progression. Positive ctDNA in the last on-treatment sample was associated with rapid progression (median 1.02 versus 3.38 yr, HR = 5.63,

Indexed as

Circulating Tumor DNAOvarian NeoplasmsCarcinoma, Ovarian EpithelialFemaleHumansNeoplasm Recurrence, LocalCirculating Tumor DNA

Identifiers

PMID38580393
PMCPMC10997860
OpenAlexW4393994558

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.