Skip to main content
Log in

Arzneimitteltherapiesicherheit in der klinischen Onkologie

Safe drug treatment in clinical oncology

  • Fokus
  • Published:
Forum Aims and scope

Zusammenfassung

In der Onkologie spielt beim Einsatz von Zytostatika, zielgerichtet wirksamen Arzneimitteln, immunmodulierend wirksamen Pharmaka (z. B. Checkpoint-Inhibitoren) und Supportivmaßnahmen die Gewährleistung einer bestmöglichen Arzneimitteltherapiesicherheit (AMTS) eine sehr wichtige Rolle. Beim Thema Arzneimittelwechselwirkungen wurden im Rahmen einer oralen Therapie substanzabhängig Interaktionen mit Magen-pH-verändernden Komedikationen oder fetthaltiger Nahrung beschrieben. Ferner können Zytochrom-P450-Inhibitoren und -induktoren die metabolische Clearance einer Reihe von Tumortherapeutika nachhaltig beeinflussen. In diesem Zusammenhang gehen auch von Produkten der komplementären und alternativen Medizin (z. B. Johanniskraut, grüner Tee) relevante Interaktionen aus. Neben Leber- und Nierenfunktionsstörungen können auch genetische Polymorphismen eine relevante Veränderung des Nebenwirkungsprofils nach sich ziehen, während geschlechtsspezifische Unterschiede in der metabolischen Clearance von Tumortherapeutika bisher von vergleichsweise untergeordneter Bedeutung sind.

Abstract

Optimization of safe drug treatment with the administration of cytostatic agents, targeted therapy drugs, immunomodulatory drugs (e.g. checkpoint inhibitors) and supportive measures, plays a pivotal role in clinical oncology. Regarding potential drug interactions with oral anticancer drugs, even changes in gastric pH or concomitant intake of fat-containing food can have a significant impact on substance-specific drug levels in plasma. In addition, coadministration of cytochrome P450 inducers and inhibitors including products for complementary and alternative medicine (CAM), e.g. green tea and St John’s wort, can significantly alter the metabolic clearance of anticancer drugs. Further aspects of safe drug treatment include appropriate dose modifications in cases of liver and kidney dysfunction as well as genetic polymorphisms, whereas gender-related effects appear to be of minor quantitative importance

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Literatur

  1. An G, Mukker JK, Derendorf H et al (2015) Enzyme- and transporter-mediated beverage-drug interactions: an update on fruit juices and green tea. J Clin Pharmacol (Epub ahead of print)

  2. Andreyev J, Ross P, Donnellan C et al (2004) Guidance on the management of diarrhoea during cancer chemotherapy. Lancet Oncol 15:447–460

    Article  Google Scholar 

  3. Blankenship P, Waddell JA (2013) Survey of carboplatin dosing strategies in oncology practise. J Am Pharm Assoc 53:420–422

    Article  Google Scholar 

  4. Chi KN, Spratlin J, Kollmannsberger C et al (2015) Food effects on abiraterone pharmacokinetics in healthy subjects and patients with metastatic castration-resistant prostate cancer. J Clin Pharmacol. doi:10.1002/jcph.5646

  5. Devriese LA, Koch KM, Mergui-Roelvink M et al (2014) Effects of low-fat and high-fat meals on steady-state pharmacokinetics of lapatinib in patients with advanced solid tumours. Invest New Drugs 32:481–488

    Article  CAS  PubMed  Google Scholar 

  6. Fagnani D, Isa L, Verga MF et al (2014) Granulocyte colony-stimulating factors used in clinical practice: PoloNord Registry-Based Cohort Italian Study. Tumori 100:491–498

    PubMed  Google Scholar 

  7. Funck-Brentano E, Alvarez JC, Longvert C et al (2015) Plasma vemurafenib concentrations in advanced BRAFV600mut melanoma patients: impact on tumour response and tolerance. Ann Oncol 26(7):1470–1405

    CAS  PubMed  Google Scholar 

  8. Gabardi S, Tullius SG, Krenzien F (2015) Understanding alterations in drug handling with aging: a focus on the pharmacokinetics of maintenance immunosuppressants in the elderly. Curr Opin Organ Tansplant 20:424–430

    Article  CAS  Google Scholar 

  9. Joshi M, Rizvi, Belani CP (2015) Afatinib for the treatment of metastatic non-small cell lung cancer. Cancer Manag Res 7:75–82

    Article  PubMed Central  PubMed  Google Scholar 

  10. Kadakia KC, Leal AD, Seisler DK et al (2014) Antiemetic prescribing practices using a computerized physician order entry system. Support Care Cancer 22:217–223

    Article  PubMed Central  PubMed  Google Scholar 

  11. Kuypers DR (2009) Immunotherapy in elderly transplant recipients: a guide to clinically significant drug interaction. Drugs Aging 26:715–737

    Article  CAS  PubMed  Google Scholar 

  12. Lam MS (2011) Extemporaneous compounding of oral liquid dosage formulations and alternative drug delivery methods for anticancer drugs. Pharmacotherapy 31:164–192

    Article  CAS  PubMed  Google Scholar 

  13. Lichtman ST, Wildiers H, Launay-Vacher V et al (2007) International Society of Geriatric Oncology (SIOG) recommendations for the adjustment of dosing in elderly cancer patients with renal insufficiency. Eur J Cancer 43:14–34

    Article  PubMed  Google Scholar 

  14. Lipp HP (2013) Klinische relevante Wechselwirkungen mit peroral applizierbaren, zielgerichtet wirksamen Tumortherapeutika. Onkologie 19:870–877

    Article  Google Scholar 

  15. Lipp HP (2007) Arzneimittelinteraktionen mit Zytostatika. Onkologe 13:801–812

    Article  Google Scholar 

  16. Lipp HP (2011) Laborwerte in der klinischen Onkologie. PZ Prisma 18:203–214

    CAS  Google Scholar 

  17. Lipp HP (2013) Tumorassoziiertes Fatigue-Syndrom (CRF). PZ Prisma 20:197–204

    CAS  Google Scholar 

  18. Lipp HP (2009) Besonderheiten der Pharmakotherapie und der Arzneimittelverordnung im Alter. In: Leischker K (Hrsg) Medizin des alternden Menschen, 1. Aufl. WVG, Stuttgart, S 77–83

  19. Ma BBY, Hui EP, Mok T (2010) Population-based differences in treatment outcome following anticancer drug therapies. Lancet Oncol 11:75–84

    Article  PubMed  Google Scholar 

  20. Pursche S, Schleyer E, Bonin M von et al (2008) Influence of enzyme-inducing antiepileptic drugs on trough level of imatinib in glioblastoma patients. Curr Clin Pharmacol 3:198–203

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  21. Leeuwen RWF van, Gelder T van, Mathijssen RH et al (2014) Drug-drug interactions with tyrosine-kinase inhibitors: a clinical perspective Lancet Oncol 15:e315–e326

  22. Werz O (2013) Mann ist nicht gleich Frau. DAZ 153:3668–3678

    Google Scholar 

  23. Widmer N, Bardin C, Chatelut E et al (2014) Review of therapeutic drug monitoring of anticancer drugs-part two targeted therapies. Eur J Cancer 8:2020–2036

    Article  Google Scholar 

  24. Yap TA, Vidal L, Adam J et al (2010) Phase I trial of the irreversible EGFR and HER2 advanced solid tumors. J Clin Oncol 28:3965–3972

    Article  CAS  PubMed  Google Scholar 

Download references

Einhaltung ethischer Richtlinien

Interessenkonflikt. H.-P. Lipp gibt an, dass kein Interessenkonflikt besteht.

Dieser Beitrag beinhaltet keine Studien an Menschen oder Tieren.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to H.-P. Lipp.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Lipp, HP. Arzneimitteltherapiesicherheit in der klinischen Onkologie. Forum 30, 517–522 (2015). https://doi.org/10.1007/s12312-015-1401-6

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12312-015-1401-6

Schlüsselwörter

Keywords

Navigation