Dr. Giesen primarily studies the drug darolutamide, which is used to treat prostate cancer. His research investigates how this drug is absorbed, metabolized, and excreted from the body, helping doctors understand its effectiveness and safety when combined with other medications. He also examines surgical methods for prostate cancer treatment, analyzing survival outcomes to identify the best practices for patients. Overall, his work aims to enhance treatment options and ensure safe medication management for individuals dealing with prostate cancer.
Key findings
In a study of 1,509 patients, darolutamide was found to not significantly interact with other medications, providing a safe treatment option for prostate cancer patients on additional therapies.
Patients undergoing robotic-assisted surgery for localized prostate cancer had a 3.9% chance of dying within five years, compared to a 5.5% chance for those who had open surgery, highlighting a survival advantage for robotic techniques.
A study showed that 95.9% of a single dose of darolutamide was recovered in urine and feces within a week, indicating its efficient elimination from the body.
Frequently asked questions
Does Dr. Giesen study the treatment of prostate cancer?
Yes, he focuses on the drug darolutamide and evaluates surgical methods for prostate cancer, aiming to optimize treatment outcomes.
What interactions has Dr. Giesen researched regarding darolutamide?
He has studied how darolutamide interacts with other medications, finding that it generally has a low risk of significant interactions, assuring safe use alongside many common drugs.
Are Dr. Giesen's findings relevant to patients receiving cancer treatments?
Yes, his work is particularly relevant for patients with prostate cancer and those undergoing various cancer treatments, as it helps inform safe medication practices.
Publications in plain English
Pharmacokinetics of Darolutamide, its Diastereomers and Active Metabolite in the Mouse: Response to Saini NK et al. (2020).
2021
Drug metabolism letters
Nykänen P, Korjamo T, Gieschen H, Zurth C, Koskinen M
Plain English This study looked at how darolutamide, a drug used for prostate cancer, behaves in mice after being given different doses over a week. It found that one form of the drug, (S,R)-darolutamide, remained in the body 3 to 5 times longer than another form, (S,S)-darolutamide. However, these differences in drug forms are not expected to impact how well the drug works in patients.
Who this helps: This helps patients with prostate cancer who are receiving darolutamide treatment.
Metabolism and Mass Balance of the Novel Nonsteroidal Androgen Receptor Inhibitor Darolutamide in Humans.
2021
Drug metabolism and disposition: the biological fate of chemicals
Taavitsainen P, Prien O, Kähkönen M, Niehues M, Korjamo T +8 more
Plain English In this study, researchers looked at how the drug darolutamide is broken down and eliminated from the body after a single dose was given to six healthy men. They found that 95.9% of the drug was recovered in urine and feces over a week, with most of it either as darolutamide or its active form, keto-darolutamide. This information is important because it helps understand how the drug works in the body and its potential interactions with other medications.
Who this helps: This helps patients needing treatment for conditions like prostate cancer, as well as their doctors in managing medication plans.
Survival After Robotic-assisted Prostatectomy for Localized Prostate Cancer: An Epidemiologic Study.
2021
Annals of surgery
Wang Y, Gieschen H, Greenberger M, Yu X, Tian G +7 more
Plain English This study looked at the survival rates of prostate cancer patients who had surgery using two different methods: robotic-assisted laparoscopic prostatectomy (RALP) and open radical prostatectomy (ORP). They found that patients who underwent RALP had a lower chance of dying within five years (3.9%) compared to those who had ORP (5.5%), translating to a significant survival advantage for RALP. This matters because it suggests that RALP not only improves survival outcomes but also helps justify its higher costs in clinical practice.
Who this helps: Patients with localized prostate cancer.
Absorption, distribution, metabolism and excretion of darolutamide (a novel non-steroidal androgen receptor antagonist) in rats.
2020
Xenobiotica; the fate of foreign compounds in biological systems
Taavitsainen P, Gieschen H, Korjamo T, Kähkönen M, Malmström C +5 more
Plain English The study looked at how darolutamide, a new drug that blocks certain hormones, is absorbed, spread throughout the body, and removed from rats. It was found that the drug is quickly absorbed after being taken by mouth, reaching peak levels in the blood within an hour. Most of it is eventually eliminated in feces (61-64%) and urine (30-33%), which helps doctors understand how to use this drug effectively in treatments.
Who this helps: This helps patients needing hormone therapy, particularly those with specific cancers.
In vivo models and decision trees for formulation development in early drug development: A review of current practices and recommendations for biopharmaceutical development.
2019
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
Zane P, Gieschen H, Kersten E, Mathias N, Ollier C +8 more
Plain English This paper reviews how pharmaceutical companies decide on drug formulations during early development, focusing on the use of animal models to predict how new drugs will behave. The study found that out of seven companies, four did not have a clear decision-making process, which could lead to missed opportunities in drug development. Understanding these processes is crucial because it helps identify potential problems early on, ensuring that new medicines are effective and safe when tested in humans.
Who this helps: This helps pharmaceutical companies and researchers improve drug development for patients.
Evaluation of Clinically Relevant Drug-Drug Interactions and Population Pharmacokinetics of Darolutamide in Patients with Nonmetastatic Castration-Resistant Prostate Cancer: Results of Pre-Specified and Post Hoc Analyses of the Phase III ARAMIS Trial.
2019
Targeted oncology
Shore N, Zurth C, Fricke R, Gieschen H, Graudenz K +11 more
Plain English This study looked at how the drug darolutamide, used for treating men with certain advanced prostate cancer, interacts with other medications that patients commonly take. Researchers found that, even though many participants (98.4% of the 1,509 included) were on multiple medications, darolutamide was not significantly affected by these drugs, including statins, and there were no notable increases in side effects from statin use in the trial. This is important because it indicates that darolutamide can be safely used alongside many other treatments without risking negative interactions.
Who this helps: This helps patients with nonmetastatic castration-resistant prostate cancer and their doctors by ensuring safe medication use.
Drug-Drug Interaction Potential of Darolutamide: In Vitro and Clinical Studies.
2019
European journal of drug metabolism and pharmacokinetics
Zurth C, Koskinen M, Fricke R, Prien O, Korjamo T +6 more
Plain English This study looked at how darolutamide, a medication for prostate cancer, interacts with other drugs in the body. Researchers found that when darolutamide was taken with itraconazole, its levels in the body increased by 75%, but they dropped by 72% when taken with rifampicin. These findings are important because they show that while darolutamide has a low risk of interacting with most drugs, it can significantly affect the levels of certain other medications, particularly those processed by specific transport proteins.
Who this helps: This information benefits doctors and healthcare providers when prescribing darolutamide alongside other medications for patients.
Plain English This study looked at certain compounds produced by mosses in peatlands to see how they stop plant growth and preserve carbon. Researchers found 655 metabolites, including 152 lipids, with 329 of these being new discoveries. They identified 17 antimicrobial compounds, primarily acids and glycosides, which could help moss control its surroundings and play a role in storing carbon, especially as climate changes.
Who this helps: This helps researchers studying ecosystems and carbon storage.
Improving the ex vivo stability of drug ester compounds in rat and dog serum: inhibition of the specific esterases and implications on their identity.
2010
Journal of pharmaceutical and biomedical analysis
Koitka M, Höchel J, Gieschen H, Borchert HH
Plain English This study looked at how certain drug compounds called esters break down in the blood serum of rats and dogs. The researchers found that three specific drug esters—sagopilone, drospirenone, and methylprednisolone aceponate—decomposed differently: sagopilone didn’t break down in dog serum at all, while drospirenone and methylprednisolone aceponate did. They identified specific enzymes responsible for this degradation and found that certain inhibitors could help stabilize these drugs, which is important for accurately measuring drug levels in preclinical studies.
Who this helps: This benefits researchers and pharmaceutical companies involved in drug development.
Determination of rat serum esterase activities by an HPLC method using S-acetylthiocholine iodide and p-nitrophenyl acetate.
2008
Analytical biochemistry
Koitka M, Höchel J, Obst D, Rottmann A, Gieschen H +1 more
Plain English This study focused on measuring the activity of certain enzymes in rat blood serum that break down molecules called esters, using a new laboratory technique known as high-performance liquid chromatography (HPLC). The researchers found that the rates at which the enzymes work are consistent, whether using two different detection methods or testing with one or both types of substrates. This matters because it means scientists can reliably use this method to assess enzyme activity in blood, which could help in understanding various health conditions.
Who this helps: This helps researchers and doctors studying enzyme-related diseases or treatments.
Characterization of new estrogen receptor destabilizing compounds: effects on estrogen-sensitive and tamoxifen-resistant breast cancer.
2004
Journal of the National Cancer Institute
Hoffmann J, Bohlmann R, Heinrich N, Hofmeister H, Kroll J +8 more
Plain English This study looked at two new drugs, ZK-703 and ZK-253, which are designed to fight breast cancer that relies on estrogen for growth, including cases that have become resistant to the common treatment tamoxifen. The researchers found that ZK-703 and ZK-253 were much more effective than tamoxifen or another drug called fulvestrant. For instance, tumors in mice treated with tamoxifen relapsed in about 10 weeks, while those treated with ZK-703 took 30 weeks to relapse.
Who this helps: These findings could benefit breast cancer patients, particularly those with tamoxifen-resistant tumors.
The bioavailability of oral fludarabine phosphate is unaffected by food.
2001
The hematology journal : the official journal of the European Haematology Association
Oscier D, Orchard JA, Culligan D, Cunningham D, Johnson S +3 more
Plain English Researchers studied how food affects the absorption and effectiveness of an oral cancer medication called fludarabine phosphate in patients with chronic lymphocytic leukemia or low-grade non-Hodgkin's lymphoma. They found that whether patients took the medication with food or on an empty stomach made little difference; 66.7% of patients responded to the treatment overall, and the absorption levels were nearly the same, with only a slight increase when taken with food. This is important because it means patients can take their medication without worrying about their meal timing.
Who this helps: Patients undergoing treatment for chronic lymphocytic leukemia and low-grade non-Hodgkin's lymphoma.
Predicting the oral bioavailability of 19-nortestosterone progestins in vivo from their metabolic stability in human liver microsomal preparations in vitro.
1998
Drug metabolism and disposition: the biological fate of chemicals
Kuhnz W, Gieschen H
Plain English This study looked at how well certain progestin drugs, specifically 19-nortestosterone types, are absorbed in the body after being taken by mouth. Researchers found that by testing these drugs in human liver samples, they could predict how well they would be absorbed, with a strong correlation for most drugs. For example, while the predicted absorption rates were about half of what was measured in real patients, the methods used showed that higher stability in the lab linked to lower absorption in the body.
Who this helps: This benefits doctors and researchers looking to prescribe or study these progestin drugs effectively.
Development of a V79 cell line expressing human cytochrome P450 2D6 and its application as a metabolic screening tool.
1997
Environmental toxicology and pharmacology
Rauschenbach R, Gieschen H, Salomon B, Kraus C, Kühne G +1 more
Plain English This study focused on creating a type of cell line that mimics how the human body processes certain drugs by using a specific enzyme called CYP2D6. Researchers successfully developed these cells and found that they could process a common medication, dextromethorphan, similarly to human liver cells, with an activity rate of 154 pmol per minute per milligram of protein. This is important because it provides a new tool for testing how different drugs are metabolized, which can help improve personalized medicine and treatment plans.
Who this helps: This benefits doctors and researchers working on drug development and personalized medicine.
Stable expression of human cytochrome P450 3A4 in V79 cells and its application for metabolic profiling of ergot derivatives.
1995
European journal of pharmacology
Rauschenbach R, Gieschen H, Husemann M, Salomon B, Hildebrand M
Plain English Researchers studied a specific human enzyme called cytochrome P450 3A4 (CYP3A4) using hamster cells to understand how this enzyme affects drug metabolism. They successfully integrated this enzyme into hamster cells and found that it converted about 6% of testosterone into a specific product, demonstrating its activity. The research also looked at two medications, lisuride and terguride, which were processed by the enzyme in these cells, showing how CYP3A4 can influence the metabolism of certain drugs.
Who this helps: This research benefits doctors and patients who depend on medications processed by this enzyme.
Studies on the biotransformation of lonazolac, bromerguride, lisuride and terguride in laboratory animals and their hepatocytes.
1989
Xenobiotica; the fate of foreign compounds in biological systems
Hümpel M, Sostarek D, Gieschen H, Labitzky C
Plain English This study looked at how four different drugs—lonazolac, bromerguride, lisuride, and terguride—are processed by the liver in different laboratory animals, including rats, guinea pigs, dogs, and monkeys. Researchers found that the drugs are broken down differently depending on the species: for example, lonazolac was the most stable, while lisuride broke down the fastest. Understanding these differences is important for developing safer and more effective treatments because it shows that how drugs work can vary greatly between animals and may not directly apply to humans.
Who this helps: This helps doctors and researchers improve drug therapies for patients.
Mikko Koskinen Olaf Prien Timo Korjamo Christian Zurth Päivi Taavitsainen Marja Kähkönen Michael Niehues Karsten Denner Pirjo Nykänen Clemens-Jeremias von Bühler
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