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Revista da Associação Médica Brasileira

Print version ISSN 0104-4230On-line version ISSN 1806-9282

Rev. Assoc. Med. Bras. vol.65 no.5 São Paulo May 2019  Epub June 03, 2019

http://dx.doi.org/10.1590/1806-9282.65.5.611 

Original Article

Evaluation of the systemic and therapeutic repercussions caused by drug interactions in oncology patients

Camila Ribeiro de Arruda Monteiro1 
http://orcid.org/0000-0002-9042-1508

Jean Henri Maselli Schoueri1 
http://orcid.org/0000-0003-2509-3592

Debora Terra Cardial1 
http://orcid.org/0000-0003-2482-4234

Lívia de Castro Linhares1 
http://orcid.org/0000-0001-8155-0634

Karine Corcione Turke1 
http://orcid.org/0000-0002-9368-1399

Lia Vineyard Steuer1 
http://orcid.org/0000-0002-0828-1949

Levy Werneck de Almeida Menezes1 
http://orcid.org/0000-0003-4248-1319

Igor Luiz Argani1 
http://orcid.org/0000-0003-3490-2961

Claudia Sette1 
http://orcid.org/0000-0001-6789-9039

Daniel de Iracema Gomes Cubero1 
http://orcid.org/0000-0002-1936-2605

Auro del Giglio1 
http://orcid.org/0000-0002-2009-824X

1Faculty of Medicine of ABC, Santo André - SP, Brasil

SUMMARY

INTRODUCTION:

Drug interaction is an important cause of global morbidity. It is of particular importance in cancer patients since they are often in use of polypharmacy, related to interactions between the drugs and the chemotherapeutics used.

OBJECTIVE:

To evaluate the drug interaction between chemotherapy and other drugs in cancer patients.

METHODS:

a cross-sectional study carried out in the outpatient oncology department of a public tertiary hospital. Two hundred thirty-five patients were included, and the drugs they were using were identified. Using the MedScape and Epocrates database, we evaluated the interactions between medications and chemotherapy by defining their frequency and dividing their severity from interaction into mild, close monitoring necessity and severe.

RESULTS:

161 patients had some drug interaction. We identified 9 types of mild interactions, 23 types of interactions with close monitoring necessity, and 2 types of serious interactions. The most frequent interactions were between fluorouracil and leucovorin (32 cases) and cyclophosphamide and doxorubicin (19 cases). Serious interactions were between aspirin and pemetrexed; and leucovorin and Bactrim.

CONCLUSION:

In the present study, drug interactions were frequent, including serious interactions with a potential increase in morbidity and mortality. Thus, it is necessary for oncologists to draw up a therapeutic plan considering potential interactions between prescribed chemotherapy and current medications in use by patients.

KEYWORDS: Drug interactions; Antineoplastic agents/adverse effects; Medical oncology

RESUMO

INTRODUÇÃO:

Interação medicamentosa é uma importante causa de morbidade mundial. Apresenta especial importância em pacientes oncológicos, pois esses frequentemente estão em uso de polifarmácia, podendo haver interações entre os medicamentos e os quimioterápicos utilizados.

OBJETIVO:

Avaliar a interação medicamentosa entre a quimioterapia e outros medicamentos em pacientes oncológicos.

MÉTODOS:

Estudo transversal realizado em serviço ambulatorial de oncologia de um hospital público terciário. Foram incluídos 235 pacientes, identificando-se quais medicamentos eram utilizados por eles. Por meio do auxílio do banco de dados do MedScape e Epocrates, avaliaram-se as interações entre as medicações e os quimioterápicos, definindo sua frequência e dividindo sua gravidade da interação em leve, monitorização próxima e grave.

RESULTADOS:

Do total estudado, 161 pacientes apresentavam alguma interação medicamentosa, sendo nove tipos de interações leves, 23 tipos de interações com necessidade de monitorização próxima e dois tipos de interações graves. As interações mais frequentes foram entre fluoracil e leucovorin (32 casos) e ciclofosfamida e doxorrubicina (19 casos). As interações sérias foram entre aspirina e pemetrexed; e leucovorim e bactrim.

CONCLUSÃO:

No presente trabalho, interações medicamentosas foram frequentes, incluindo interações graves com potencial aumento de morbimortalidade. Assim, faz-se necessário que oncologistas tracem um plano terapêutico levando em consideração as possíveis interações medicamentosas entre a quimioterapia prescrita e demais medicações em uso pelos pacientes.

PALAVRAS-CHAVE: Interações medicamentosas; Antineoplásicos/efeitos adversos; Oncologia

INTRODUCTION

According to the World Health Organization (WHO), drug interaction is the main cause of morbidity and mortality in the world.1 Data indicate that, in the United States, annually, over 2 million of patients who are hospitalized suffer from adverse reactions to drugs, and approximately 100,000 die from it. Drug interaction, defined as an increase or reduction of the clinical effect of a given drug due to the interference of another, it is responsible for about 3% to 5% of these cases.2 This is because drug interactions can interfere in both pharmacokinetics and pharmacodynamics by inducing or inhibiting cytochrome P450, which can lead to a synergistic, additive or antagonistic effect of some drugs, thus compromising their effectiveness.3

In general, the patients who are mostly exposed to this scenario are those who make use of polypharmacy, such as oncology patients, who need to make use of drugs not only to treat the cancer itself, but also due to the toxicity induced by the treatment and syndromes related to neoplasia, in addition to the drugs used for possible comorbidities.4

In addition, several studies have investigated drugs with the potential to interfere with chemotherapy, showing remarkable rates of drug interaction.59 As an example, it is known that drugs used to treat psychiatric disorders such as carbamazepine, phenytoin, phenobarbital, primidone, and valproic acid interact with chemotherapy treatments in general.6 Other drugs such as fentanyl, midazolam, captopril, and potassium chloride have also shown a high prevalence of drug interaction.10

However, the main problem lies in the use of drugs whose effects on treatment are unknown and which are often bought without restrictions by the patients, who self-medicate, usually without informing the oncologist.11.12

Similarly, van Leeuwen et al.7 predicted that over half of the patients in the use of chemotherapeutic agents present some kind of drug interaction, and a third of them suffer serious consequences.13

Due to this scenario, it is necessary to know the drugs that have the potential to interfere with the efficacy of chemotherapeutic agents, so that oncologists can draw a plan of action more accurate and individualized in order to improve the treatment offered to the patients.

OBJECTIVES

General objective

Assess drug interaction between chemotherapy and other drugs that are taken by cancer patients, with or without medical guidance.

Specific objectives

Assess the adverse effects resulting from drug interactions that might interfere with the prognosis and quality of life of patients under antineoplastic treatment.

List the drugs whose interaction is identified by this study.

Assess the effects of the drug interactions found.

METHODS

Study design

This is a cross-sectional study that analyzed patients treated by the Oncology Service linked to the FMABC (State Hospital Mário Covas, in Santo André and School Hospital Padre Anchieta, in São Bernardo do Campo). The patients were invited to participate in the study, with a previous explanation that their participation was voluntary and that their personal information would remain confidential.

We considered eligible for the study patients with age greater than or equal to 18 years, able to read and understand Portuguese and who were or were to be submitted to chemotherapy. We excluded from the study all patients younger than 18 years old, illiterate and who had not undergone chemotherapy or had no indication of a chemotherapy regimen.

After approval by the ethics committee, 235 patients were included in this study, which was based on data collection by means of an interview in which the patient answered open questions and in the evaluation of possible interactions between the drugs reported with the aid of Epocrates And MedScape applications. These free electronic applications for smartphones use, exclusively, the names of medications taken by each patient, indicating, when present, the possibility of interaction between them. The use of the applications was done by the researchers of this study, who reported the information to the participants. The information relating to the current chemotherapeutic treatment were obtained from the records of each individual patient.

After signing the Informed Consent Form - ICF, patients filled out an identification form with their clinical and demographic data, as well as a questionnaire in which they should indicate the drugs used by them: those who used without medical guidance as well as those prescribed, besides their chemotherapeutic agents.

The questionnaire contains general data of the patient, as staging of neoplasia, previous surgery, beginning of chemotherapy; clinical data, in which the drugs taken were disclosed, as well as the doses administered and an assessment of signs and symptoms based on the information referring to the treatment during chemotherapy; and complementary data, obtained by means of a simpler questions, aiming to evaluate all drugs used, their dosage and symptoms.

The researcher, at the time of inclusion, was responsible for clarifying the purpose of the study and assisting the subjects in answering the questionnaires.

In relation to the risks and benefits, the present study had a minimal risk in relation to the emotional context of the patient, since it caused them to reflect on questions that involve the disease, but there were no risks related to the physical health of patients. In addition, there is an indirect benefit from the implementation of future projects which, based on the collected data, can contribute to the improvement of the quality of life of these patients.

RESULTS

The present study included 235 patients. Of these, 161 had some drug interaction in accordance with the criterion of Epocrates. Their sociodemographic characteristics are presented in Table 1.

TABLE 1 SOCIODEMOGRAPHIC DATA 

N = 161
Gender Female 62 38.5%
Male 99 61.5%
Age Mean 61 years
Interval 27 to 85 years
Marital status Single 45 27.9%
Married 100 62.1%
Widow(er) 16 9.9%
Formal education Illiterate 6 3.7%
Incomplete elementary school 66 40.9%
Complete elementary school 18 11.1%
Incomplete secondary school 10 6.2%
Complete secondary school 40 24.8%
Incomplete undergraduate program 11 6.8%
Complete undergraduate program 10 6.2%
Ethnicity White 92 57.1%
Brown 37 22.9%
Black 18 11.1%
Indigenous 8 4.9%
Others 6 3.7%
Occupation Works 58 36.0%
Does not work 103 63.9%
Origin The ABC region 144 89.4%
Others 17 10.5%
Site of the primary neoplasia Head and neck 7 4.3%
Lung 13 8.0%
Gastrointestinal tract 58 36.0%
Urinary tract 8 4.9%
Gynecologic 50 31.0%
Others 25 15.5%

We then excluded interactions that did not involve chemotherapy drugs, dividing them remaining between “chemotherapy and chemotherapy” or “chemotherapy and non-chemotherapy. The interactions found and their frequency are shown in Table 2.

TABLE 2 ANALYSIS OF DEGREES OF INTERACTIONS 

Chemotherapy vs. Non-chemotherapy Chemotherapy vs. Chemotherapy
Chemotherapy Non-chemotherapy Frequency Chemotherapy drugs Frequency
Vincristine Prednisone 4 Cisplatin + Paclitaxel 3
Docetaxel Prednisone 2
Dexamethasone 2
Primidone 1
Paclitaxel Budesonide 1
Captopril 1
Glimepiride Prednisone 1
Aspirin 1
Paclitaxel Losartan 6 Fluorouracil + Leucovorin 32
Dexamethasone 4 Cyclophosphamide + Doxorubicin 19
Simvastatin 3 Paclitaxel + Doxorubicin 7
Phenytoin 1 Paclitaxel + Trastuzumab 3
Rosuvastatin 1 Irinotecan + Bevacizumab 2
Cyclosporine 1 Paclitaxel + Lapatinib 1
Cyclophosphamide Enoxaparin 1 Cisplatin + Cyclophosphamide 1
Allopurinol 1 Cisplatin Decarbazine 1
Doxorubicin Dexamethasone 2 Fluorouracil + Bevacizumab 1
Docetaxel Simvastatin 2
Irinotecan Dexamethasone 2
Bortezomib Omeprazole 1
Etoposide Dexamethasone 1
Eloxatin Zidovudine 1
Pemetrexed Acetylsalicylic Acid 1
Leucovorin Bactrim 1

The interactions were divided into “mild”, “close monitoring” and “serious”, as shown in the “drug interaction Checker” of MedScape. In the chemotherapy vs. non-chemotherapy group, we found eight types of mild interactions, 14 that required close monitoring and two considered serious. Whereas in the chemotherapy vs. chemotherapy group, we found a mild interaction, nine interactions with the need for close monitoring and no serious interaction. The results can be found in Table 3.

TABLE 3 SEVERITY OF INTERACTIONS 

Severity of interaction Chemotherapy vs. Non-chemotherapy (Unexpected interactions) Chemotherapy vs. Chemotherapy (Expected interaction)
Mild Vincristine Prednisone Cisplatin + Paclitaxel
Docetaxel Prednisone; Dexamethasone Primidone
Paclitaxel Budesonide; Captopril
Close monitoring Glimepiride Prednisone; Aspirin Fluorouracil + Leucovorin
Paclitaxel Losartan; Dexamethasone Simvastatin; Phenytoin Rosuvastatin; Cyclosporine Cyclophosphamide + Doxorubicin
Cyclophosphamide Enoxaparin; Allopurinol Paclitaxel + Trastuzumab
Doxorubicin Dexamethasone Irinotecan + Bevacizumab
Docetaxel Simvastatin Paclitaxel + Lapatinib
Irinotecan Dexamethasone
Bortezomib Omeprazole
Etoposide Dexamethasone
Eloxatin Zidovudine
Severe Pemetrexed Acetylsalicylic acid
Leucovorin Bactrim

DISCUSSION

In oncological treatment, the concern with possible drug interactions should always be raised by the oncologist. It is worth noting that certain interactions are expected and may even be desired, especially in regard to interactions between chemotherapy drugs, between which there is a synergism of action, for example. In this context, we can cite as examples of known interactions 5-fluorouracil and leucovorin14, or doxorubicin/cyclophosphamide followed by paclitaxel15.

Also in the context of the expected associations, the most prevalent drug interaction was between fluorouracil and leucovorin (32 cases), and it occurs during the antineoplastic treatment, with increased toxicity of the medication due to the effect of pharmacodynamic synergism. The same goes for the second most frequent drug interaction, cyclophosphamide, and doxorubicin.16

The third most frequent interaction, paclitaxel and doxorubicin, even though it was already expected to have increased toxicity related to their combined use bringing an improved oncologic prognosis16, it should be mentioned that the interaction between them includes increased levels of doxorubicin, considering the decrease of renal clearance of creatinine generated by paclitaxel.16 Thus, it is observed that associations of chemotherapeutic agents may present, concomitantly, intentional drug interactions associated to harmful interactions.

Among the serious interactions, the one between aspirin (acetylsalicylic acid; ASA) and pemetrexed is noteworthy. Pemetrexed is a chemotherapeutic agent indicated for the treatment of non-small cell lung cancer,17 while acetylsalicylic acid is used as secondary prophylaxis of new cardiovascular events18. Considering the frequency of concomitance of these comorbidities, both in part secondary to smoking19, there is the possibility of a same patient receiving the association of pemetrexed and ASA. Despite this, these medications should not be associated, since aspirin increases the levels of pemetrexed due to decreased renal excretion of the chemotherapeutic agent. It is worth mentioning that this association should be undertaken with caution in patients with normal renal function (creatinine clearance > 80 ml/min) and avoided in patients with preserved renal function, because, due to this factor, aspirin can raise the levels of pemetrexed and cause adverse events.20

To avoid such interaction, one possibility would be to replace acetylsalicylic acid by another antiplatelet agent that also causes reduction of cardiovascular risk during the period of oncological treatment, such as clopidogrel21, which presents no drug interactions with the pemetrexed16.

Another serious interaction was found between leucovorin and Bactrim (trimethoprim and sulfamethoxazole). Leucovorin corresponds to a drug used, among other reasons, in association with fluorouracil, for adjuvant chemotherapeutic treatment of colorectal cancer and for recovery in patients treated with high doses of methotrexate22.23. Bactrim, in turn, corresponds to an antibiotic often used for infectious prophylaxis in oncologic patients who are immunosuppressed during the chemotherapy treatment24. Thus, there is the possibility of the same patient using both drugs simultaneously, and leucovorin decreases the effect of trimethoprim due to a mechanism of pharmacodynamic antagonism.16

To avoid the interaction between leucovorin and Bactrim, the antibiotic can be replaced for another that is effective and does not interact with the leucovorin.24.25

As discussed, it is observed that drugs used for oncologic therapy are not an exception in the context of drug interactions. In addition, these drugs have important cytotoxic effects and feature many pharmacokinetic and pharmacodynamic variations among patients. As noted, the use of combinations and the number of drugs involved in the treatment increases the likelihood of such interactions.26

Thus, the presence of drug interactions among cancer patients is noteworthy. In this scenario, in addition to the associations made intentionally by oncologists with the purpose of increasing the effectiveness of the treatment, there are also those that occur without the supervision of these professionals, arising mainly from drugs taken without informing the medical team.

Furthermore, oncology patients are particularly prone to polypharmacy2729, making use of several drugs simultaneously. Thus, in addition to the greater risk of drug interactions, more than one interaction can be present in the same patient, increasing the possibility of unwanted effects and worsen prognosis2729.

An important example of multiple interactions in oncologic patients corresponds to that of chemotherapeutic agents, such as paclitaxel associated with simvastatin and losartan, drugs widely prescribed in older patients30.31. Although beneficial in isolation, paclitaxel presents drug interaction with both other drugs, with the need for close monitoring16. Simvastatin and losartan lead to unwanted increases in the levels of paclitaxel, increasing its toxicity; paclitaxel brings an increased risk of myopathy related to simvastatin.16 Multiple interactions such as this should be carefully assessed by the oncologist, especially in patients in use of multiple drugs simultaneously.

The serious interactions found were between aspirin and pemetrexed, and leucovorin and Bactrim. Although the present study has found only individual cases of the concomitant use of drugs with serious drug interaction, this can probably be explained by the limitation of the small number of patients included, since the high prevalence of the use of these medications18.24 indicates that the frequency of unwanted interactions is possibly even higher. Thus, it reinforces the idea that physicians should be alert to the possible effects from such interactions and how they vary according to each patient, which can result in a worse prognosis for patients in neoplastic treatment.

CONCLUSION

Drug interactions were frequent in oncologic patients. Although the majority of interactions was related to the synergistic effect already expected between chemotherapy drugs, there were unexpected serious interactions and interactions with the need of close monitoring The main interactions found were the severe increase of chemotherapy toxicity due to the worsening of renal function, which may increase the mortality related to the treatment; and the reduction of the effect of antibiotic medication, related to an increased risk of bacterial infection and, consequently, an increase in mortality.

Thus, it is necessary that oncologists create a therapy plan considering possible drug interactions between the chemotherapy prescribed and other drugs used by the patients in order to ensure a better oncologic prognosis.

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Received: May 14, 2018; Accepted: May 26, 2018

CORRESPONDING AUTHOR: Igor Argani Rua Lauro Gomes, 2000 – Santo Andre – São Paulo – Brasil – 09060-650 E-mail: igorargani@hotmail.com

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