Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-5222
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dc.contributor.authorBeck, Olaf-
dc.contributor.authorParet, Claudia-
dc.contributor.authorRusso, Alexandra-
dc.contributor.authorBurhenne, Jürgen-
dc.contributor.authorFresnais, Margaux-
dc.contributor.authorSteimel, Kevin-
dc.contributor.authorSeidmann, Larissa-
dc.contributor.authorWagner, Daniel-Christoph-
dc.contributor.authorVewinger, Nadine-
dc.contributor.authorLehmann, Nadine-
dc.contributor.authorSprang, Maximilian-
dc.contributor.authorBackes, Nora-
dc.contributor.authorRoth, Lea-
dc.contributor.authorNeu, Marie Astrid-
dc.contributor.authorWingerter, Arthur-
dc.contributor.authorHenninger, Nicole-
dc.contributor.authorEL Malki, Khalifa-
dc.contributor.authorOtto, Henrike-
dc.contributor.authorAlt, Francesca-
dc.contributor.authorDesuki, Alexander-
dc.contributor.authorKindler, Thomas-
dc.contributor.authorFaber, Jörg-
dc.date.accessioned2020-10-20T10:51:21Z-
dc.date.available2020-10-20T10:51:21Z-
dc.date.issued2020-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/5226-
dc.description.abstractAbstract: Osteosarcoma (OS) is the second most common cause of cancer-related death in pediatric patients. The insulin-like growth factor (IGF) pathway plays a relevant role in the biology of OS but no IGF targeted therapies have been successful as monotherapy so far. Here, we tested the e ect of three IGF specific inhibitors and tested ceritinib as an o -target inhibitor, alone or in combination with dasatinib, on the proliferation of seven primary OS cells. Picropodophyllin, particularly in combination with dasatinib and the combination ceritinib/dasatinib were e ective in abrogating the proliferation. The ceritinib/dasatinib combination was applied to the primary cells of a 16-year-old girl with a long history of lung metastases, and was more e ective than cabozantinib and olaparib. Therefore, the combination was used to treat the patient. The treatment was well tolerated, with toxicity limited to skin rush and diarrhea. A histopathological evaluation of the tumor after three months of therapy indicated regions of high necrosis and extensive infiltration of macrophages. The extension of the necrosis was proportional to the concentration of dasatinib and ceritinib in the area, as analysed by an ultra performance liquid chromatography–tandem mass spectrometer (UPLC-MS/MS). After the cessation of the therapy, radiological analysis indicated a massive growth of the patient’s liver metastases. In conclusion, these data indicate that the combination of ceritinib/dasatinib is safe and may be used to develop new therapy protocols.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizin Mainzde
dc.language.isoengde
dc.rightsCC BY-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleSafety and activity of the combination of ceritinib and dasatinib in osteosarcomaen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-5222-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.number2700-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleCancersde
jgu.journal.volume12de
jgu.journal.issue4de
jgu.pages.alternativeArt. 793de
jgu.publisher.year2020-
jgu.publisher.nameMDPIde
jgu.publisher.placeBaselde
jgu.publisher.urihttps://doi.org/10.3390/cancers12040793de
jgu.publisher.issn2072-6694de
jgu.organisation.placeMainz-
jgu.subject.ddccode610de
jgu.publisher.doi10.3390/cancers12040793
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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