Evidence map›Paper›PMID 36749424›Full record

ReviewJournal of cancer research and clinical oncology2023

NOTCH3 missense mutations as predictor of long-term response to gemcitabine in a patient with epithelioid hemangioendothelioma.

Moritz Schmidt, Sven Mattern, Stephan Singer, Martin Schulze, Saskia Biskup, Patrick Krumm, Ulrich M Lauer, Lars Zender, Clemens Hinterleitner, Martina Hinterleitner

Open access · hybridAbstract readCase ReportsReview
In one paragraph

Review in Journal of cancer research and clinical oncology, 2023. 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, top 99% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

10 authors at 4 institutions in 2 countries.

Moritz SchmidtDepartment of Medical Oncology and Pneumology (Internal Medicine VIII), University Hospital Tuebingen, 72076, Tuebingen, Germany.
Sven MatternDepartment of Pathology, University Hospital Tuebingen, Tuebingen, Germany.
Stephan SingerDepartment of Pathology, University Hospital Tuebingen, Tuebingen, Germany.
Martin SchulzePraxis Für Humangenetik Tübingen, Tuebingen, Germany.
Saskia BiskupPraxis Für Humangenetik Tübingen, Tuebingen, Germany.
Patrick KrummDepartment of Radiology, University Hospital Tuebingen, Tuebingen, Germany.
Ulrich M LauerDepartment of Medical Oncology and Pneumology (Internal Medicine VIII), University Hospital Tuebingen, 72076, Tuebingen, Germany.
Lars ZenderDepartment of Medical Oncology and Pneumology (Internal Medicine VIII), University Hospital Tuebingen, 72076, Tuebingen, Germany.
Clemens HinterleitnerDepartment of Medical Oncology and Pneumology (Internal Medicine VIII), University Hospital Tuebingen, 72076, Tuebingen, Germany.
Martina HinterleitnerDepartment of Medical Oncology and Pneumology (Internal Medicine VIII), University Hospital Tuebingen, 72076, Tuebingen, Germany. martina.hinterleitner@med.uni-tuebingen.de.
University of Tübingen · DECeGaT (Germany) · DEMemorial Sloan Kettering Cancer Center · USPraxis für Humangenetik Tübingen · DE

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeEpithelioid hemangioendothelioma (EHE) as a very rare malignant vascular tumor belongs to the heterogenous group of soft-tissue sarcomas. Depending on the clinical course of the disease, interdisciplinary treatment concepts are required, including surgery, radiotherapy and systemic cancer therapy. However, due to its uncommonness, standard treatment options are lacking so far, especially in advanced disease with distant metastases. METHODS AND

resultsHere we report on an unusual case of a patient with metastasized EHE showing long-term response to second line treatment with gemcitabine over almost 2 decades. Cancer genome sequencing of the patient's tumor tissue detected a NOTCH3 missense mutation which could provide an explanation for these clinical findings. NOTCH3 is known to be a mediator of resistance towards gemcitabine-based cancer treatment, at least in pancreatic cancer and non-small cell lung cancer.

conclusionThe observation that this missense mutation of NOTCH3 is associated with an increased response to treatment with gemcitabine in EHE can be used prospectively to assess NOTCH3 as potential biomarker for predicting therapy response to gemcitabine.

Indexed as

Carcinoma, Non-Small-Cell LungHemangioendothelioma, EpithelioidLung NeoplasmsGemcitabineHumansMutation, MissenseReceptor, Notch3GemcitabineNOTCH3 protein, humanReceptor, Notch3Epithelioid hemangioendotheliomaGemcitabineNOTCH3Soft-tissue sarcoma

Identifiers

PMID36749424
PMCPMC10356887
OpenAlexW4319334329

What OpenQuestion holds

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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.