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Christian Dittrich
Researcher at University of Vienna
Publications - 98
Citations - 3645
Christian Dittrich is an academic researcher from University of Vienna. The author has contributed to research in topics: Breast cancer & Chemotherapy. The author has an hindex of 28, co-authored 95 publications receiving 3281 citations.
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Phase II Study of Temsirolimus (CCI-779), a Novel Inhibitor of mTOR, in Heavily Pretreated Patients With Locally Advanced or Metastatic Breast Cancer
Stephen Chan,Max E. Scheulen,Stephen S. Johnston,Klaus Mross,Fatima Cardoso,Christian Dittrich,Wolfgang Eiermann,Dagmar Hess,Rudolph Morant,Vladimir Semiglazov,Markus Borner,Marc Salzberg,Valerijus Ostapenko,Hans-Joachim Illiger,Dirk Behringer,Nathalie Bardy-Bouxin,Joseph Boni,S. Kong,Maria Cincotta,Laurence Moore +19 more
TL;DR: In heavily pretreated patients with locally advanced or metastatic breast cancer, 75 and 250 mg temsirolimus showed antitumor activity and 75 mg Temsiro Limus showed a generally tolerable safety profile.
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Phase II Study of Imatinib in Patients With Recurrent Gliomas of Various Histologies: A European Organisation for Research and Treatment of Cancer Brain Tumor Group Study
Eric Raymond,Alba A. Brandes,Christian Dittrich,Pierre Fumoleau,Bruno Coudert,Paul Clement,Marc Frenay,Roy Rampling,Roger Stupp,Johan M. Kros,Michael Heinrich,Thierry Gorlia,Denis Lacombe,Martin J. van den Bent +13 more
TL;DR: In the dose range of 600 to 1,000 mg/d, single-agent imatinib is well tolerated but has limited antitumor activity in patients with recurrent gliomas.
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Detection of EpCAM positive and negative circulating tumor cells in metastatic breast cancer patients.
Robert Königsberg,Eva Obermayr,Giovanna Bises,Georg Pfeiler,Margit Gneist,Fritz Wrba,Maria De Santis,Robert Zeillinger,Marcus Hudec,Christian Dittrich +9 more
TL;DR: EpCAM independent enrichment technologies seem to be superior to detect the entire CTC population, and evaluation of CTCs as prognostic marker should compromise EpCAM (+) and (−) subpopulations.
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Pharmacokinetics of a novel anticancer ruthenium complex (KP1019, FFC14A) in a phase I dose-escalation study.
Frederike Lentz,A. Drescher,Andreas Lindauer,Magdalena Henke,Ralf A. Hilger,Christian G. Hartinger,Max E. Scheulen,Christian Dittrich,Bernhard K. Keppler,Ulrich Jaehde +9 more
TL;DR: Seven patients with various types of solid tumours refractory to standard therapy were treated with escalating doses of KP1019 twice weekly for 3 weeks, and the pharmacokinetic disposition was characterised by a small volume of distribution, low clearance and long half-life.
Journal ArticleDOI
Efficacy of BGJ398, a Fibroblast Growth Factor Receptor 1-3 Inhibitor, in Patients with Previously Treated Advanced Urothelial Carcinoma with FGFR3 Alterations.
Sumanta K. Pal,Jonathan E. Rosenberg,Jean H. Hoffman-Censits,Raanan Berger,David I. Quinn,Matthew D. Galsky,Juergen Wolf,Christian Dittrich,Bhumsuk Keam,Jean Pierre Delord,Jan H.M. Schellens,Gwenaelle Gravis,J. Medioni,Pablo Maroto,Virote Sriuranpong,Chaiyut Charoentum,Howard A. Burris,Viktor Grünwald,Daniel P. Petrylak,Ulka N. Vaishampayan,Eliahu Gez,Ugo De Giorgi,Jae-Lyun Lee,Jens Voortman,Sumati Gupta,Sunil Sharma,Amir Mortazavi,David J. Vaughn,Randi Isaacs,Katie Parker,Xueying Chen,Kun Yu,Dale Porter,Diana Graus Porta,Dean F. Bajorin +34 more
TL;DR: BJJ398 is active in patients with alterations in FGFR3, resulting in both reductions in tumor volume and stabilization of disease, highlighting putative mechanisms of resistance to the agent, which may be useful in following disease status.