Accès ouvert
2026
article
OpenAlex
Michael Karl Melzer, Angelika Mattigk, Verena I. Gaidzik, Nadine Therese Gaisa et autres
Epididymal and rete testis tumors are exceedingly rare. We report a 69-year-old male who presented with progressive swelling of the right testis/epididymis; histopathology confirmed clear cell carcinoma of the rete testis. Staging with FDG-PET-CT revealed bilateral pulmonary metastases. Subsequent gene panel sequencing …
de
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Accès ouvert
2025
article
OpenAlex
Maria‐Veronica Teleanu, Christoph E. Heilig, Sebastian Pirmann, Rainer Hamacher et autres
BACKGROUND: This study aims to evaluate antitumor response of palbociclib in patients with advanced chordoma, an ultra-rare cancer without approved systemic therapy. Previous data showed that palbociclib reduced cell viability and proliferation in CDKN2A-deficient chordoma cell lines. PATIENTS AND METHODS: We conducted …
de
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Accès ouvert
2025
erratum
OpenAlex
Siyer Roohani, Jolina Handtke, Kamal Hummedah, Markus Albertsmeier et autres
In this article, the author’s name Armin Tuchscherer was incorrectly written as Armin Tuscherer. The original article has been corrected.
de, at
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Accès ouvert
2025
article
OpenAlex
Carolin Seeling, Sonja Dahlum, Ralf Marienfeld, Vera Jan et autres
BACKGROUND: Li-Fraumeni syndrome (LFS) is an autosomal dominant tumor predisposition syndrome characterized by a high familial incidence of various malignancies. It results from pathogenic/likely pathogenic heterozygous constitutional variants of the TP53 gene. Due to impaired DNA damage repair, conventional cytotoxic therapies or …
de
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Accès ouvert
2025
article
OpenAlex
Siyer Roohani, Jolina Handtke, Kamal Hummedah, Markus Albertsmeier et autres
PURPOSE: The management of soft tissue sarcoma (STS) at reference centers with specialized multidisciplinary tumor boards (MTB) improves patient survival. The German Cancer Society (DKG) certifies sarcoma centers in German-speaking countries, promoting high standards of care. This study investigated the variability in …
de, at
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Accès ouvert
2025
article
OpenAlex
Sibylle Cocciardi, Maral Saadati, Nina Weiß, Daniela Späth et autres
ABSTRACT This study aimed to evaluate the impact of the myelodysplasia‐related gene (MRG) as well as additional gene mutations on outcomes in intensively treated patients with NPM1‐mutated (NPM1mut) AML. Targeted DNA sequencing of 263 genes was performed in 568 NPM1mut AML patients …
de, us
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Accès ouvert
2025
preprint
OpenAlex
Christoph E. Heilig, Christoph Heining, E. Gnutzmann, Sandra Roldan et autres
de
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Accès ouvert
2025
article
OpenAlex
Christoph E. Heilig, Christoph Heining, E. Gnutzmann, Sandra Roldan et autres
BACKGROUND: Desmoplastic small round cell tumor (DSRCT) and synovial sarcoma (SySa) are rare cancers primarily affecting adolescents and young adults. Prognosis is generally poor, particularly upon metastasis, due to limited efficacy of chemotherapies and the lack of molecular mechanism-based approaches. Recently, overexpression …
de
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Accès ouvert
2024
article
OpenAlex
Stephan Ursprung, Wolfgang Thaiss, Janina Beha, Yvonne Möller et autres
Background/Objectives: Current guidelines recommend Cisplatin/Gemcitabine/Durvalumab as first-line treatment for inoperable or recurrent cholangiocarcinoma (CCA). Molecular tumor boards (MTB) have the expertise to support organ-specific tumor boards with evidence-based treatment recommendations for subsequent lines of treatment, based on genomic tumor data and scientific …
de
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Accès ouvert
2024
article
OpenAlex
Verena I. Gaidzik
Die randomisierte LMS04 Studie der French Sarcoma Group zeigte, dass die Kombinationstherapie aus Doxorubicin und Trabectedin, gefolgt von einer Trabectedin-Erhaltungstherapie, das Gesamtüberleben (33 versus 24 Monate) und das progressionsfreie Überleben (12 versus 6 Monate) im Vergleich zur alleinigen Doxorubicin-Therapie bei Patient*innen mit …
de
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2024
article
OpenAlex
Johannes Schulze, Andreas Sakkas, Sebastian Pietzka, Frank Wilde et autres
de
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Accès ouvert
2024
article
OpenAlex
Frank G. Rücker, Lars Bullinger, Sibylle Cocciardi, Sabrina Skambraks et autres
ABSTRACT: Measurable residual disease (MRD) monitoring in acute myeloid leukemia (AML) with an FLT3 internal tandem duplication (FLT3-ITDpos) has been hampered by the broad heterogeneity of ITD mutations. Using our recently developed FLT3-ITD paired-end next-generation sequencing (NGS)-based MRD assay (limit of detection …
de
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