Evidence map›Paper›PMID 41749865›Full record

ArticleCancers2026

Incidence and Survival of Thoracic Angiosarcoma: Epidemiologic Evidence from a Population-Based Cancer Registry.

Niels Michael Dörr-Jerat, Ina Wellmann, Franziska Rees, Marcus Krüger, Hiltraud Kajüter, Andreas Stang

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Niels Michael Dörr-JeratDepartment of Thoracic Surgery, Martha-Maria Hospital Halle-Dölau, 06120 Halle, Germany.ORCID 0000-0002-6544-6607
Ina WellmannCancer Registry of North Rhine-Westphalia, 44801 Bochum, Germany.
Franziska ReesCancer Registry of North Rhine-Westphalia, 44801 Bochum, Germany.
Marcus KrügerDepartment of Thoracic Surgery, Martha-Maria Hospital Halle-Dölau, 06120 Halle, Germany.ORCID 0000-0001-5250-5658
Hiltraud KajüterCancer Registry of North Rhine-Westphalia, 44801 Bochum, Germany.
Andreas StangCancer Registry of North Rhine-Westphalia, 44801 Bochum, Germany.ORCID 0000-0001-6363-9061

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThoracic angiosarcoma is a very rare and malignant disease. This study examined the incidence and survival of thoracic angiosarcomas with special focus on primary and secondary angiosarcomas.

methodsData from the population-based North Rhine-Westphalia (NRW) cancer registry in Germany covering the years 2008-2023 were analyzed, including primary and secondary thoracic angiosarcoma (ICD-O-3: morphology 9120/3, topography C34, C38, C44.51, C49.3, C50), and reported age-standardized incidence rates (using the Old European Standard population) and survival analyses (Kaplan-Meier curves).

resultsA total of 421 cases of thoracic angiosarcoma were analyzed, and 90.0% of the patients were female (

conclusionsThoracic angiosarcoma is a rare condition with a poor prognosis. Irrespective of whether their disease is classified as primary or second primary, women with angiosarcoma have a better prognosis than men. Topography seems to be the most determining prognostic factor in this disease.

Indexed as

angiosarcomaincidencerare malignancysurvivalthorax

Identifiers

PMID41749865
PMCPMC12939740

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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.