B
Benjamin Weide
Researcher at University of Tübingen
Publications - 132
Citations - 10305
Benjamin Weide is an academic researcher from University of Tübingen. The author has contributed to research in topics: Melanoma & Antigen. The author has an hindex of 39, co-authored 129 publications receiving 7891 citations. Previous affiliations of Benjamin Weide include German Cancer Research Center.
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Journal ArticleDOI
Survival after intratumoral interleukin-2 treatment of 72 melanoma patients and response upon the first chemotherapy during follow-up
Benjamin Weide,Thomas Eigentler,Annette Pflugfelder,Ulrike Leiter,Friedegund Meier,Jürgen Bauer,Diethard Schmidt,Peter Radny,Claudia Pföhler,Claus Garbe +9 more
TL;DR: Patients with cutaneous metastasis without lymph node involvement in stage III and with soft-tissue metastasis in stage IV showed unexpected favorable survival rates after intratumoral treatment with IL-2, associated with increased complete and partial responses in subsequent chemotherapies.
Journal ArticleDOI
Tumor microenvironment-derived S100A8/A9 is a novel prognostic biomarker for advanced melanoma patients and during immunotherapy with anti-PD-1 antibodies
Nikolaus B. Wagner,Benjamin Weide,Mirko Gries,Mirko Gries,Maike Reith,Maike Reith,Kathrin Tarnanidis,Kathrin Tarnanidis,Valerie Schuermans,Valerie Schuermans,Charlotte Kemper,Charlotte Kemper,Coretta Kehrel,Coretta Kehrel,Anne Funder,Anne Funder,Ramtin Lichtenberger,Ramtin Lichtenberger,Antje Sucker,Esther Herpel,Tim Holland-Letz,Dirk Schadendorf,Claus Garbe,Viktor Umansky,Viktor Umansky,Jochen Utikal,Jochen Utikal,Christoffer Gebhardt,Christoffer Gebhardt +28 more
TL;DR: The tumor microenvironment-associated protein S100A8/A9 serves as a novel prognostic marker for metastasis and survival of metastatic melanoma patients and predicts response to immunotherapy with pembrolizumab, underscoring the significance of tumor micro environment-derived factors as suitable biomarkers for melanoma.
Journal ArticleDOI
Differential influence of vemurafenib and dabrafenib on patients’ lymphocytes despite similar clinical efficacy in melanoma
Bastian Schilling,Wiebke Sondermann,Fang Zhao,Klaus G. Griewank,Elisabeth Livingstone,Antje Sucker,Henning Zelba,Benjamin Weide,Uwe Trefzer,Tabea Wilhelm,Carmen Loquai,Carola Berking,Jessica C. Hassel,Katharina C. Kähler,Jochen Utikal,Jochen Utikal,P. Al Ghazal,Ralf Gutzmer,Simone M. Goldinger,Lisa Zimmer,Annette Paschen,Uwe Hillen,Dirk Schadendorf +22 more
TL;DR: In this article, the authors explored the impact of selective BRAF inhibitors on the hosts' immune system using flow cytometry and multiplex assays, and found that vemurafenib but not dabrafenib decreases patients peripheral lymphocyte counts and alters CD4 + T cell phenotype and function.
Journal ArticleDOI
The Generation of CAR-Transfected Natural Killer T Cells for the Immunotherapy of Melanoma.
Bianca Simon,Manuel Wiesinger,Johannes März,Kilian Wistuba-Hamprecht,Benjamin Weide,Beatrice Schuler-Thurner,Gerold Schuler,Jan Dörrie,Ugur Uslu +8 more
TL;DR: It is feasible to generate CAR-NKT cells by using mRNA electroporation, and their CAR-mediated cytotoxicity is at least equal to that of conventional CAR-T cells, while their intrinsic cytotoxic activity is maintained.
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Cancer immunotherapy is accompanied by distinct metabolic patterns in primary and secondary lymphoid organs observed by non-invasive in vivo 18 F-FDG-PET.
Johannes Schwenck,Johannes Schwenck,Barbara F. Schörg,Francesco Fiz,Francesco Fiz,Dominik Sonanini,Dominik Sonanini,Andrea Forschner,Thomas Eigentler,Benjamin Weide,Manuela Martella,Irene Gonzalez-Menendez,Cristina Campi,Gianmario Sambuceti,Ferdinand Seith,Leticia Quintanilla-Martinez,Claus Garbe,Christina Pfannenberg,Martin Röcken,Martin Röcken,Christian la Fougère,Christian la Fougère,Bernd J. Pichler,Bernd J. Pichler,Bernd J. Pichler,Manfred Kneilling,Manfred Kneilling +26 more
TL;DR: It is demonstrated that the widely available 18F-FDG-PET modality is an applicable translational tool that has high potential to stratify patients at an early time point and is capable of detecting immunotherapy-associated metabolic changes in the primary and secondary lymphoid organs induced by the systemic immune response after CIT.