Research Topics
Species | Klaus MrossSummaryAffiliation: University of Freiburg Country: Germany Publications
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Detail Information
Publications
Results from an in vitro and a clinical/pharmacological phase I study with the combination irinotecan and sorafenibK Mross
Tumour Biology Center at the Albert Ludwigs University, Freiburg, Germany
Eur J Cancer 43:55-63. 2007....
Phase I clinical and pharmacokinetic study of BBR 3576, a novel aza-anthrapyrazole, administered i.v. every 4 weeks in patients with advanced solid tumors: a phase I study group trial of the Central European Society of Anticancer-Drug Research (CESAR)Klaus Mross
Tumor Biology Center Albert Ludwigs University, Freiburg, Germany
Anticancer Drugs 15:15-22. 2004..This trial showed that BBR 3576 has a manageable toxicity profile on a 4-week schedule. Phase II studies have started in patients with solid tumors, as suggested by preclinical data in different in vivo model systems...
Pharmacokinetics of liposomal doxorubicin (TLC-D99; Myocet) in patients with solid tumors: an open-label, single-dose studyKlaus Mross
Tumor Biology Center, Albert Ludwigs University Freiburg, 79106, Freiburg im Breisgau, Germany
Cancer Chemother Pharmacol 54:514-24. 2004..We conducted an open-label phase I study to determine the pharmacokinetic profile of a single dose of liposome-encapsulated doxorubicin (Myocet) in patients with various solid tumors. Safety and tolerability were monitored...
Drug-drug interaction pharmacokinetic study with the Raf kinase inhibitor (RKI) BAY 43-9006 administered in combination with irinotecan (CPT-11) in patients with solid tumorsK Mross
Tumor Biology Center, Albert-Ludwigs-University Freiburg, Germany
Int J Clin Pharmacol Ther 41:618-9. 2003
Phase I clinical and pharmacokinetic study of PTK/ZK, a multiple VEGF receptor inhibitor, in patients with liver metastases from solid tumoursKlaus Mross
Tumour Biology Center at the Albert Ludwigs University Freiburg, Breisacher Strasse 117, D 79106 Freiburg i Br, Germany
Eur J Cancer 41:1291-9. 2005..The minimum biologically active dose was established at 750 mg/day whereas the recommended dose for phase III studies is 1200 mg/day...
[Inhibition of the VEGF receptor system with tyrosine kinase inhibitors. Angiogenesis inhibition in oncology]Klaus Mross
, Breisacherstrasse 117, D-79106 Freiburg iBr
Pharm Unserer Zeit 37:404-15. 2008
Phase I dose escalation and pharmacokinetic study of BI 2536, a novel Polo-like kinase 1 inhibitor, in patients with advanced solid tumorsKlaus Mross
Tumor Biology Center at the Albert Ludwigs University Freiburg, Breisacherstrasse 117, D 79106, Freiburg, Germany
J Clin Oncol 26:5511-7. 2008..The aim of this trial was to identify the maximum tolerated dose (MTD) of BI 2536 and to determine the safety, pharmacokinetics, and antitumor activity in patients who had advanced solid tumors...
Comparison of 1-hour and 3-hours paclitaxel infusion pharmacokinetics: results from a randomized trialK Mross
Department of Medical Oncology, Tumor Biology Center, Albert Ludwigs University Freiburg, Germany
Onkologie 25:503-8. 2002..Aim of this study was to characterize the difference in pharmacokinetics (PK) of paclitaxel (PAC) after 1-h and 3-h infusion in humans and to define a pharmacodynamic relationship between PAC PK and myelotoxicity...
Flat dose (175 mg/weekly) paclitaxel: pharmacokinetics and clinical implicationsK Mross
Tumor Biology Center, Albert Ludwigs University Freiburg, Germany
Int J Clin Pharmacol Ther 43:601-2. 2005
PAC fixed dose: pharmacokinetics of a 1-hour paclitaxel infusion and comparison to BSA-normalized drug dosingKlaus Mross
Department of Medical Oncology, Tumor Biology Center at the Albert Ludwigs University, Germany
Onkologie 29:444-50. 2006....
Phase I study of the angiogenesis inhibitor BIBF 1120 in patients with advanced solid tumorsKlaus Mross
Tumour Biology Center and Department of Radiology, Section MR Development, Albert Ludwigs Universitat Freiburg, Freiburg, Germany
Clin Cancer Res 16:311-9. 2010..Dynamic contrast-enhanced magnetic resonance imaging assessed antiangiogenic effect in 42 patients...
[Clinical trials: prerequisite of evidence-based oncology: reality, perspectives and a new tool recruited--the Internet]K Mross
Klinik für Tumorbiologie an der Albert Ludwigs Universität, Freiburg i Br
Onkologie 24:24-34. 2001..This will be more than an incremental step forward to deliver the best possible clinical care towards the ultimate goal: to deliver evidence-based medicine en route to a cure for more cancer patients than ever...
[Chemotherapy of colonic carcinoma in the year 2001]K Mross
Klinik fur Tumorbiologie, Albert Ludwig Universität Freiburg
Praxis (Bern 1994) 90:497-510. 2001..The median survival of patients with metastatic colon cancer is between 12 and 18 month. It will be discussed in which way this range depends on the chemotherapeutical strategy...
Clinical trials with anti-angiogenic agents in hematological malignanciesMichael Medinger
Department of Medical Oncology, Tumor Biology Center at the Albert Ludwigs University, Breisacherstrasse 117, D 79106 Freiburg, Germany
J Angiogenes Res 2:10. 2010..This review summarizes recent advances in the basic understanding of the role of angiogenesis in hematological malignancies and clinical trials with novel therapeutic approaches targeting angiogenesis...
The pharmacokinetics of a 1-h paclitaxel infusionK Mross
Department of Medical Oncology and Clinical Pharmacology, Tumor Biology Center at the Albert Ludwigs University Freiburg, Germany
Cancer Chemother Pharmacol 45:463-70. 2000..To characterize the disposition of paclitaxel (PAC) after a 1-h infusion in humans and define if possible a pharmacodynamic relationship between PAC disposition and the observed toxicity...
Phase I study of telatinib (BAY 57-9352): analysis of safety, pharmacokinetics, tumor efficacy, and biomarkers in patients with colorectal cancerKlaus Mross
Tumor Biology Center at the Albert Ludwigs University Freiburg, Germany
Vasc Cell 3:16. 2011..abstract:..
Metronomic antiangiogenic therapy with capecitabine and celecoxib in advanced tumor patients--results of a phase II studySimone Steinbild
Tumor Biology Center at the Albert Ludwigs University Freiburg and MR Development and Application Center of the University Hospital, Freiburg, Germany
Onkologie 30:629-35. 2007..Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) was used to monitor antiangiogenic effects...
A phase IA, open-label, dose-escalating study of PTK787/ZK 222584 administered orally on a continuous dosing schedule in patients with advanced cancerJoachim Drevs
Tumor Biology Center, Albert Ludwigs University Freiburg, Breisacherstrasse 117, 79106 Freiburg, Germany
Anticancer Res 30:2335-9. 2010..PTK787/ZK 222584 (PTK/ZK) offers a novel approach to inhibit tumour angiogenesis...
Paclitaxel pharmacokinetics and response to chemotherapy in patients with advanced cancer treated with a weekly regimenStephan Mielke
Department of Hematology and Oncology, University of Freiburg Medical Center, Freiburg i Br, Germany
Anticancer Res 25:4423-7. 2005..Paclitaxel pharmacokinetics were shown to be related to toxicity and survival. Patients and..
Phase I and pharmacokinetic study of the (6-maleimidocaproyl)hydrazone derivative of doxorubicinClemens Unger
Department Medical Oncology, Tumor Biology Center, Freiburg, Germany
Clin Cancer Res 13:4858-66. 2007..The purpose of the phase I study was to characterize the toxicity profile of DOXO-EMCH, establish a recommended dose for phase II studies, and assess potential anticancer activity...
Phase I clinical study of AZD2171, an oral vascular endothelial growth factor signaling inhibitor, in patients with advanced solid tumorsJoachim Drevs
Tumor Biology Center, MR Development and Application Center, Albert Ludwigs University, Freiburg, Germany
J Clin Oncol 25:3045-54. 2007..This phase I study was designed to evaluate the safety and tolerability of increasing doses of AZD2171, with additional assessments of pharmacokinetics, pharmacodynamics, and efficacy...
First-time-in-man and pharmacokinetic study of weekly oral perifosine in patients with solid tumoursClemens Unger
Klinik für Tumorbiologie an der Albert Ludwigs Universität, Freiburg, Germany
Eur J Cancer 46:920-5. 2010..To identify the maximum-tolerated dose (MTD) and pharmacokinetics of oral perifosine...
Regression of cutaneous tumor lesions in patients intratumorally injected with a recombinant single-chain antibody-toxin targeted to ErbB2/HER2Marc Azemar
Tumor Biology Center, Freiburg, Germany
Breast Cancer Res Treat 82:155-64. 2003..No hematologic, renal, and/or cardiovascular toxicities were noted. Our results demonstrate that local therapy with scFv(FRP5)-ETA can be effective against ErbB2 expressing tumors justifying further clinical development of this reagent...
Association of Paclitaxel pharmacokinetics with the development of peripheral neuropathy in patients with advanced cancerStephan Mielke
Department of Hematology and Oncology, University of Freiburg Medical Center, Freiburg, Germany
Clin Cancer Res 11:4843-50. 2005..05 micromol/L (T >0.05) remains almost constant. As both Cremophor EL and paclitaxel are neurotoxic, we evaluated their pharmacodynamic effects on the development of peripheral neuropathy as the most important nonhematologic toxicity...
Phase II STUdy with 3rd- or 4th-line bendamustine (flat dose) therapy in patients with metastatic breast cancerSimone Steinbild
Tumor Biology Center at the Albert Ludwigs University Freiburg, Freiburg, Germany
Onkologie 32:488-92. 2009..Bendamustine is a drug with a favorable side effect spectrum and it offers a chance to overcome tumor resistance in pretreated patients with metastatic breast cancer (MBC)...
Treatment of anthracycline extravasation with dexrazoxane -- clinical experienceAnnette Frost
Tumor Biology Center at the Albert Ludwigs University, Freiburg i.Br, Germany
Onkologie 29:314-8. 2006..RESULTS: The 2 patients treated with dexrazoxane recovered completely without any sequelae. CONCLUSIONS: Treatment of antracycline extravasation with dexrazoxane is potentially useful and safe...
Peripheral neuropathy: a persisting challenge in paclitaxel-based regimesStephan Mielke
Department of Hematology and Oncology, University of Freiburg Medical Center, Freiburg i Br, Germany
Eur J Cancer 42:24-30. 2006..In this report we review and discuss the pathogenesis, incidence, risk factors, diagnosis, pharmacodynamics and treatment options for PAC-induced PNP...
Gemcitabine and interferon-alpha 2b in solid tumors: a phase I study in patients with advanced or metastatic non-small cell lung, ovarian, pancreatic or renal cancerStefan Fuxius
Tumor Biology Center, Albert Ludwigs University Freiburg, 79106 Freiburg i Br, Germany
Anticancer Drugs 13:899-905. 2002..The results, particularly those in metastatic renal carcinoma, are encouraging and worthy of further evaluation in phase II trials...
Phase II study of combined 5-fluorouracil/ Ginkgo biloba extract (GBE 761 ONC) therapy in 5-fluorouracil pretreated patients with advanced colorectal cancerB Hauns
Department of Medical Oncology, Tumor Biology Center at the Albert-Ludwigs-University Freiburg, Breisacher Str. 117, D-79106 Freiburg i. Br, Germany
Phytother Res 15:34-8. 2001..Since an improvement was observed in some patients despite the failure of the conventional 5-FU pretreatment, it would be interesting to evaluate whether the application of 5-FU plus GBE 761 ONC as a first line treatment is of benefit...
c-kit (CD117) expression in human tumors and its prognostic value: an immunohistochemical analysisMichael Medinger
Tumor Biology Center, Albert Ludwigs University Freiburg, Freiburg im Breisgau, Germany
Pathol Oncol Res 16:295-301. 2010..Expression of c-kit was found in tumor samples with varying intensities and infrequently...
Clinical phase I study with one-hour paclitaxel infusionK Mross
Department of Medical Oncology and Clinical Pharmacology, Tumor Biology Center at the Albert Ludwigs University Freiburg, Germany
Ann Oncol 9:569-72. 1998..We evaluated a one-hour infusion schedule within a phase I study to determine the dose limiting toxicity (DLT), the maximum tolerated dose (MTD), and the anti-cancer efficacy...
Soluble markers for the assessment of biological activity with PTK787/ZK 222584 (PTK/ZK), a vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitor in patients with advanced colorectal cancer from two phase I trialsJ Drevs
Tumor Biology Center, Freiburg, Germany
Ann Oncol 16:558-65. 2005....
A phase I clinical and pharmacokinetic study of the camptothecin glycoconjugate, BAY 38-3441, as a daily infusion in patients with advanced solid tumorsK Mross
Department of Medical Oncology, Tumor Biology Center at the University of Freiburg, Berlin, Germany
Ann Oncol 15:1284-94. 2004..However, because of the superior safety profile, we recommend the 3-day schedule for BAY 38-3441 at a dose of 320 mg/m2/day as 30-min infusions for further phase II studies...
A clinical phase II study with sorafenib in patients with progressive hormone-refractory prostate cancer: a study of the CESAR Central European Society for Anticancer Drug Research-EWIVS Steinbild
Tumor Biology Center, Albert Ludwigs University Freiburg Freiburg, Germany
Br J Cancer 97:1480-5. 2007..Sorafenib has antitumour activity in HRPCP when evaluated for RECIST- and PSA-based response. Further investigation as a component of combination regimens is necessary to evaluate its definite or overall clinical benefit for HRPCP...
DCE-MRI in clinical trials: data acquisition techniques and analysis methodsR Strecker
University Hospital, Albert Ludwigs University, Freiburg, Germany
Int J Clin Pharmacol Ther 41:603-5. 2003
Serial measurements of pharmacokinetics, DCE-MRI, blood flow, PET and biomarkers in serum/plasma--what is a useful tool in clinical studies of anti-angiogenic drugs?K Mross
Tumor Biology Center at the Albert Ludwigs University Freiburg, Germany
Int J Clin Pharmacol Ther 40:573-4. 2002
Comparative pharmacokinetics of unbound paclitaxel during 1- and 3-hour infusionsHans Gelderblom
Department of Medical Oncology, Rotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital Rotterdam, Rotterdam, The Netherlands
J Clin Oncol 20:574-81. 2002....
Dynamic contrast-enhanced magnetic resonance imaging as a biomarker for the pharmacological response of PTK787/ZK 222584, an inhibitor of the vascular endothelial growth factor receptor tyrosine kinases, in patients with advanced colorectal cancer and livBruno Morgan
University of Leicester, United Kingdom
J Clin Oncol 21:3955-64. 2003....
Comparative neurotoxicity of weekly non-break paclitaxel infusions over 1 versus 3 hStephan Mielke
Department of Hematology and Oncology, University of Freiburg Medical Center, Germany
Anticancer Drugs 14:785-92. 2003..A majority of patients experiencing neurotoxic effects require the investigation of potential nerve protectors in future clinical trials accompanying PAC therapy...
Phase II study of temsirolimus (CCI-779), a novel inhibitor of mTOR, in heavily pretreated patients with locally advanced or metastatic breast cancerStephen Chan
Department of Clinical Oncology, Nottingham City Hospital, Hucknall Rd, Nottingham N65 1PB, United Kingdom
J Clin Oncol 23:5314-22. 2005....
Association of CYP2C8, CYP3A4, CYP3A5, and ABCB1 polymorphisms with the pharmacokinetics of paclitaxelAnja Henningsson
Department of Pharmaceutical Biosciences, Faculty of Pharmacy, Uppsala University, Uppsala, Sweden
Clin Cancer Res 11:8097-104. 2005..To retrospectively evaluate the effects of six known allelic variants in the CYP2C8, CYP3A4, CYP3A5, and ABCB1 genes on the pharmacokinetics of the anticancer agent paclitaxel (Taxol)...
Association of ABCB1 genotypes with paclitaxel-mediated peripheral neuropathy and neutropeniaTristan M Sissung
Clinical Pharmacology Research Core, National Cancer Institute, 9000 Rockville Pike, Building 10, Room 5A01, Bethesda, MD 20892, USA
Eur J Cancer 42:2893-6. 2006..This pilot study suggests that paclitaxel-induced neuropathy and neutropenia might be linked to inherited variants of ABCB1 through a mechanism that is unrelated to altered plasma pharmacokinetics...
