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Published in: International Journal of Clinical Pharmacy 5/2010

01-10-2010 | Research Article

Potential drug–drug interactions between anti-cancer agents and community pharmacy dispensed drugs

Authors: Marsha L. Voll, Kim D. Yap, Wim E. Terpstra, Mirjam Crul

Published in: International Journal of Clinical Pharmacy | Issue 5/2010

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Abstract

Objective of the study To identify the prevalence of potential drug–drug interactions between hospital pharmacy dispensed anti-cancer agents and community pharmacy dispensed drugs. Setting A retrospective cohort study was conducted on the haematology/oncology department of the internal medicine ward in a large teaching hospital in Amsterdam, the Netherlands. Method Prescription data from the last 100 patients treated with anti-cancer agents were obtained from Paracelsus, the chemotherapy prescribing system in the hospital. The community pharmacy dispensed drugs of these patients were obtained by using OZIS, a system that allows regionally linked pharmacies to call up active medication on any patient. Both medication lists were manually screened for potential drug–drug interactions by using several information sources on interactions, e.g. Pubmed, the Flockhart P450 table, Micromedex and Dutch reference books. Main outcome measure Prevalence of potential drug–drug interactions between anti-cancer agents provided by the hospital pharmacy and drugs dispensed by the community pharmacy. Results Ninety-one patients were included in the study. A total of 31 potential drug–drug interactions were found in 16 patients, of which 15 interactions were clinically relevant and would have required an intervention. Of these interactions 1 had a level of severity ≥D, meaning the potential drug–drug interaction could lead to long lasting or permanent damage, or even death. The majority of the interactions requiring an intervention (67%) had a considerable level of evidence (≥2) and were based on well-documented case reports or controlled interaction studies. Most of the potential drug–drug interactions involved the antiretroviral drugs (40%), proton pump inhibitors (20%) and antibiotics (20%). The anti-cancer drug most involved in the drug–drug interactions is methotrexate (33%). Conclusion This study reveals a high prevalence of potential drug–drug interactions between anti-cancer agents provided by the hospital pharmacy and drugs dispensed by the community pharmacy. It shows us there is need for an optimal medication surveillance mechanism to detect potential drug–drug interactions between these two groups of medication, especially because of the high toxicity of anticancer drugs and thus the severe consequences these interactions can have for the patient.
Literature
1.
go back to reference Riechelmann RP, Tannock IF, Wang L, Saad ED, Taback NA, Krzyzanowska MK. Potential drug interactions and duplicate prescriptions among cancer patients. J Natl Cancer Inst. 2007;99(8):592–600.CrossRefPubMed Riechelmann RP, Tannock IF, Wang L, Saad ED, Taback NA, Krzyzanowska MK. Potential drug interactions and duplicate prescriptions among cancer patients. J Natl Cancer Inst. 2007;99(8):592–600.CrossRefPubMed
2.
go back to reference Jaehde U, Liekweg A, Simons S, Westfeld M. Minimising treatment-associated risks in systemic cancer therapy. Pharm World Sci. 2008;30:161–8.CrossRefPubMed Jaehde U, Liekweg A, Simons S, Westfeld M. Minimising treatment-associated risks in systemic cancer therapy. Pharm World Sci. 2008;30:161–8.CrossRefPubMed
3.
go back to reference Paracelsus© Version 1.9. 2008. Farmaco-Logica, Onnen, The Netherlands. Paracelsus© Version 1.9. 2008. Farmaco-Logica, Onnen, The Netherlands.
4.
go back to reference Stoop AP, Bal R, Berg M. OZIS and the politics of safety: Using ICT to create a regionally accessible patient medication record. Int J Med Inf. 2007;76:229–35.CrossRef Stoop AP, Bal R, Berg M. OZIS and the politics of safety: Using ICT to create a regionally accessible patient medication record. Int J Med Inf. 2007;76:229–35.CrossRef
9.
go back to reference Koninklijke Nederlandse Maatschappij ter bevordering der Pharmacie, Geneesmiddel Informatie Centrum. Informatorium Medicamentorum. The Hague: KNMP;2009 [Dutch]. Koninklijke Nederlandse Maatschappij ter bevordering der Pharmacie, Geneesmiddel Informatie Centrum. Informatorium Medicamentorum. The Hague: KNMP;2009 [Dutch].
10.
go back to reference de Gier JJ. Commentaren medicatiebewaking 2008/2009. Houten: Health Base; 2008. [Dutch]. de Gier JJ. Commentaren medicatiebewaking 2008/2009. Houten: Health Base; 2008. [Dutch].
11.
go back to reference College voor zorgverzekeringen. Farmacotherapeutisch Kompas 2009. Houten: Bohn Stafleu Van Loghum; 2009. [Dutch]. College voor zorgverzekeringen. Farmacotherapeutisch Kompas 2009. Houten: Bohn Stafleu Van Loghum; 2009. [Dutch].
12.
go back to reference Uttamsingh V, Lu C, Miwa G, Gan L. Relative contributions of the five major human cytochromes P450, 1A2, 2C9, 2C19, 2D6, and 3A4, to the hepatic metabolism of the proteasome inhibitor bortezomib. Drug Metab Dispos. 2005;33(11):1723–8.CrossRefPubMed Uttamsingh V, Lu C, Miwa G, Gan L. Relative contributions of the five major human cytochromes P450, 1A2, 2C9, 2C19, 2D6, and 3A4, to the hepatic metabolism of the proteasome inhibitor bortezomib. Drug Metab Dispos. 2005;33(11):1723–8.CrossRefPubMed
13.
go back to reference Zhou S. Drugs behave as substrates, inhibitors and inducers of human cytochrome P450 3A4. Curr Drug Metab. 2008;9:310–22.CrossRefPubMed Zhou S. Drugs behave as substrates, inhibitors and inducers of human cytochrome P450 3A4. Curr Drug Metab. 2008;9:310–22.CrossRefPubMed
15.
go back to reference Vaccher E, Spina M, di Gennaro G, Talamini R, Nasti G, Schioppa O, et al. Concomitant cyclophosphamide, doxorubicin, vincristine, and prednisone chemotherapy plus highly active antiretroviral therapy in patients with human immunodeficiency virus-related, non-hodgkin lymphoma. Cancer. 2001;91(1):155–63.CrossRefPubMed Vaccher E, Spina M, di Gennaro G, Talamini R, Nasti G, Schioppa O, et al. Concomitant cyclophosphamide, doxorubicin, vincristine, and prednisone chemotherapy plus highly active antiretroviral therapy in patients with human immunodeficiency virus-related, non-hodgkin lymphoma. Cancer. 2001;91(1):155–63.CrossRefPubMed
16.
go back to reference Toffoli G, Corona G, Cattarossi G, Boiocchi M, di Gennaro G, Tirelli U, et al. Effect of highly active antiretroviral therapy (HAART) on pharmacokinetics and pharmacodynamics of doxorubicin in patients with HIV-associated non-Hodgkin’s lymphoma. Ann Oncol. 2004;15:1805–9.CrossRefPubMed Toffoli G, Corona G, Cattarossi G, Boiocchi M, di Gennaro G, Tirelli U, et al. Effect of highly active antiretroviral therapy (HAART) on pharmacokinetics and pharmacodynamics of doxorubicin in patients with HIV-associated non-Hodgkin’s lymphoma. Ann Oncol. 2004;15:1805–9.CrossRefPubMed
17.
go back to reference Candussio L, Decorti G, Crivellato E, Granzotto M, Rosati A, Giraldi T, et al. Toxicologic and pharmacokinetic study of low doses of verapamil combined with doxorubicin. Life Sci. 2002;71:3109–19.CrossRefPubMed Candussio L, Decorti G, Crivellato E, Granzotto M, Rosati A, Giraldi T, et al. Toxicologic and pharmacokinetic study of low doses of verapamil combined with doxorubicin. Life Sci. 2002;71:3109–19.CrossRefPubMed
18.
go back to reference Antoniou T, Tseng AL. Interactions between antiretrovirals and antineoplastic drug therapy. Clin Pharmacokinet. 2005;44(2):111–45.CrossRefPubMed Antoniou T, Tseng AL. Interactions between antiretrovirals and antineoplastic drug therapy. Clin Pharmacokinet. 2005;44(2):111–45.CrossRefPubMed
19.
go back to reference Windle R, MacPherson S, Bell PRF. Neutropenia associated with metronidazole. Br Med J. 1979;2:1219.CrossRefPubMed Windle R, MacPherson S, Bell PRF. Neutropenia associated with metronidazole. Br Med J. 1979;2:1219.CrossRefPubMed
20.
go back to reference Bardakji Z, Jolivet J, Langelier Y, Besner J, Ayoub J. 5-Fluorouracil-metronidazole combination therapy in metastatic colorectal cancer. Cancer Chemother Pharmacol. 1986;18:140–4.CrossRefPubMed Bardakji Z, Jolivet J, Langelier Y, Besner J, Ayoub J. 5-Fluorouracil-metronidazole combination therapy in metastatic colorectal cancer. Cancer Chemother Pharmacol. 1986;18:140–4.CrossRefPubMed
21.
go back to reference Ferrazzini G, Klein J, Sulh H, Chung D, Griesbrecht E, Koren G. Interaction between trimethoprim-sulfamethoxazole and methotrexate in children with leukaemia. J Pediatr. 1990;117(5):823–6.CrossRefPubMed Ferrazzini G, Klein J, Sulh H, Chung D, Griesbrecht E, Koren G. Interaction between trimethoprim-sulfamethoxazole and methotrexate in children with leukaemia. J Pediatr. 1990;117(5):823–6.CrossRefPubMed
22.
go back to reference Steuer A, Gumpel JM. Methotrexate and trimethoprim: a fatal interaction. Br J Rheumatol. 1998;37:105–6.CrossRefPubMed Steuer A, Gumpel JM. Methotrexate and trimethoprim: a fatal interaction. Br J Rheumatol. 1998;37:105–6.CrossRefPubMed
23.
go back to reference Ng HWK, MacFarlane AW, Graham RM, Verbov JL. Near fatal drug interactions with methotrexate given for psoriasis. Br Med J (Clin Res Ed). 1987;295(6601):752–3.CrossRef Ng HWK, MacFarlane AW, Graham RM, Verbov JL. Near fatal drug interactions with methotrexate given for psoriasis. Br Med J (Clin Res Ed). 1987;295(6601):752–3.CrossRef
24.
go back to reference Suzuki K, Doki K, Homma M, Tamaki H, Hori S, Ohtani H, et al. Co-administration of proton pump inhibitors delays elimination of plasma methotrexate in high-dose methotrexate therapy. Br J Clin Pharmacol. 2008;67(1):44–9.CrossRefPubMed Suzuki K, Doki K, Homma M, Tamaki H, Hori S, Ohtani H, et al. Co-administration of proton pump inhibitors delays elimination of plasma methotrexate in high-dose methotrexate therapy. Br J Clin Pharmacol. 2008;67(1):44–9.CrossRefPubMed
25.
go back to reference Joerger M, Huitema ADR, van den Bongerd HJGD, Baas P, Schornagel JH, Schellens JHM, Beijnen JH. Determinants of the elimination of methotrexate and 7-hydroxy-methotrexate following high-dose infusional therapy to cancer patients. Br J Clin Pharmacol. 2005;62(1):71–80.CrossRef Joerger M, Huitema ADR, van den Bongerd HJGD, Baas P, Schornagel JH, Schellens JHM, Beijnen JH. Determinants of the elimination of methotrexate and 7-hydroxy-methotrexate following high-dose infusional therapy to cancer patients. Br J Clin Pharmacol. 2005;62(1):71–80.CrossRef
26.
go back to reference Tröger U, Stötzel B, Martens-Lobenhoffer J, Gollnick H, Meyer FP. Severe myalgia from an interaction between treatments with pantoprazole and methotrexate. Br Med J. 2002;324:1497.CrossRef Tröger U, Stötzel B, Martens-Lobenhoffer J, Gollnick H, Meyer FP. Severe myalgia from an interaction between treatments with pantoprazole and methotrexate. Br Med J. 2002;324:1497.CrossRef
27.
go back to reference Bauters TGM, Verlooy J, Robays H, Laureys G. Interactions between methotrexate and omeprazole in an adolescent with leukemia: a case report. Pharm World Sci. 2008;30:316–8.CrossRefPubMed Bauters TGM, Verlooy J, Robays H, Laureys G. Interactions between methotrexate and omeprazole in an adolescent with leukemia: a case report. Pharm World Sci. 2008;30:316–8.CrossRefPubMed
28.
go back to reference Reid T, Yuen A, Catolico M, Carlson RW. Impact of omeprazole on the plasma clearance of methotrexate. Cancer Chemother Pharmacol. 1993;33:82–4.CrossRefPubMed Reid T, Yuen A, Catolico M, Carlson RW. Impact of omeprazole on the plasma clearance of methotrexate. Cancer Chemother Pharmacol. 1993;33:82–4.CrossRefPubMed
29.
go back to reference Appelo DA, Berger-De Jong IEJ, Janssen MJA. Effect van preoperatieve farmacotherapeutische opnamegesprekken op de kwaliteit van het medicatieoverzicht op een orthopedische afdeling. Pharm Weekbl. 2008;3:8–13. [Dutch]. Appelo DA, Berger-De Jong IEJ, Janssen MJA. Effect van preoperatieve farmacotherapeutische opnamegesprekken op de kwaliteit van het medicatieoverzicht op een orthopedische afdeling. Pharm Weekbl. 2008;3:8–13. [Dutch].
Metadata
Title
Potential drug–drug interactions between anti-cancer agents and community pharmacy dispensed drugs
Authors
Marsha L. Voll
Kim D. Yap
Wim E. Terpstra
Mirjam Crul
Publication date
01-10-2010
Publisher
Springer Netherlands
Published in
International Journal of Clinical Pharmacy / Issue 5/2010
Print ISSN: 2210-7703
Electronic ISSN: 2210-7711
DOI
https://doi.org/10.1007/s11096-010-9410-0

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