Evidence map›Paper›PMID 37522200›Full record

ArticleCancer biomarkers : section A of Disease markers2023

Prognostic value of ALK overexpression and molecular abnormalities in high-grade serous ovarian carcinoma.

Adam Gorczyński, Kevin Miszewski, Yann Gager, Sonja Koch, Jane Pötschke, Dimitar Ugrinovski, Jörg Gabert, Agata Pospieszyńska, Dariusz Wydra, Renata Duchnowska and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

17 authors at 4 institutions in 2 countries.

Adam GorczyńskiDepartment of Pathomorphology, Medical University of Gdansk, Gdansk, Poland.
Kevin MiszewskiDepartment of Urology, Medical University of Gdansk, Gdansk, Poland.
Yann GagerParoX GmbH, Leipzig, Germany.
Sonja KochPathoNext GmbH, Leipzig, Germany.
Jane PötschkePathoNext GmbH, Leipzig, Germany.
Dimitar UgrinovskiPathoNext GmbH, Leipzig, Germany.
Jörg GabertPathoNext GmbH, Leipzig, Germany.
Agata PospieszyńskaDepartment of Gynecology, Obstetrics and Neonatology, Medical University of Gdansk, Gdansk, Poland.
Dariusz WydraDepartment of Gynecology, Obstetrics and Neonatology, Medical University of Gdansk, Gdansk, Poland.
Renata DuchnowskaDepartment of Oncology, Military Institute of Medicine, National Research Institute, Warsaw, Poland.
Bartosz SzymanowskiDepartment of Oncology, Military Institute of Medicine, National Research Institute, Warsaw, Poland.
Szczepan CierniakDepartment of Pathology, Military Institute of Medicine, National Research Institute, Warsaw, Warsaw, Poland.
Irene KrueckenPathoNext GmbH, Leipzig, Germany.
Karsten NeumannInstitute of Pathology, Staedtisches Klinikum Dessau, Brandenburg Medical School Theodor Fontane, Dessau, Germany.
Katarina MirkovInstitute of Pathology, Staedtisches Klinikum Dessau, Brandenburg Medical School Theodor Fontane, Dessau, Germany.
Wojciech BiernatDepartment of Pathomorphology, Medical University of Gdansk, Gdansk, Poland.
Piotr CzapiewskiInstitute of Pathology, Staedtisches Klinikum Dessau, Brandenburg Medical School Theodor Fontane, Dessau, Germany.
Gdańsk Medical University · PLStädtisches Klinikum Dessau · DEWojskowy Instytut Medycyny Lotniczej · PLLeipzig University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundALK receptor tyrosine kinase (ALK) aberrations have an established role in pathogenesis of many neoplasms, but their clinical significance in high grade serous ovarian carcinoma (HGSOC) is unclear.

objectiveTo analyse the frequency of ALK overexpression, molecular abnormalities of ALK, and their impact on the progression-free survival (PFS) and overall survival (OS) in HGSOC.

methodsProtein expression was examined by immunohistochemistry (IHC) using three different clones of anti-ALK antibody. The presence of translocations was analysed using fluorescent in situ hybridization. Next-generation sequencing was used for studying the copy number variation, as well as point mutation and translocations involving other commonly rearranged genes.

resultsALK overexpression was demonstrated in up to 52% of tumours, whereas ALK copy gains in 8.2%, with no clear impact on survival. ALK point mutations were identified in 13 tumours (8.9%), with 3 belonging to the class IV showing significantly better OS. A trend suggesting better PFS was also noticed in these cases. Additionally, three gene fusions were found: ERBB2-GRB7, PRKCA-BRCA1 and SND1-BRAF, none of which has been previously described in HGSOC.

conclusionsHGSOC harbouring activating ALK mutations might be associated with a better survival, while ALK overexpression and ALK amplification does not impact the prognosis.

Indexed as

DNA Copy Number VariationsOvarian NeoplasmsEndonucleasesFemaleHumansIn Situ Hybridization, FluorescencePrognosisTranslocation, GeneticEndonucleasesSND1 protein, humanBRAFBRCA1ERBB2fusionpoint mutations

Identifiers

PMID37522200
PMCPMC12412845
OpenAlexW4385406031

What OpenQuestion holds

Textmetadata
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.