Abstract
Background
The risk of drug–drug interactions (DDI) has become a major issue in cancer patients. However, data in sarcoma patients are scarce. We aimed to evaluate the frequency and the factors associated with DDI with antitumor treatments, and to evaluate the impact of a pharmacist evaluation before anticancer treatment.
Patients and methods
We performed a retrospective review of consecutive sarcoma patients starting chemotherapy (CT) or Tyrosine kinase inhibitor (TKI). A pharmacist performed medication reconciliation and established an early toxicity risk assessment. Potential DDI with antitumor drugs were identified using Micromedex electronic software.
Results
One hundred and twenty-two soft-tissue and 80 bone sarcoma patients (103 males, median age 50 years,) were included before CT (86%) or TKI (14%). The median number of medications was 3; 34 patients (22% of patients with medication reconciliation) reported complementary medicine use. 37 potential DDI classified as major, were identified (12% of the 243 pre-therapeutic assessments). In multivariate analysis, TKI (p < 0.0001), proton pump inhibitor (p = 0.026) and antidepressant (p < 0.001) were identified as risk factors of DDI (p < 0.02). Only marital status (p = 0.003) was associated with complementary medicine use. A pharmacist performed 157 medication reconciliations and made 71 interventions among 59 patients (37%). In multivariate analysis, factors associated with pharmacist intervention were: complementary medicines (p = 0.004), drugs number (p = 0.005) and treatment with TKI (p = 0.0002)
Conclusions
Clinical interventions on DDI are more frequently required among sarcoma patients treated with TKI than CT. Multidisciplinary risk assessment including a medication reconciliation by a pharmacist could be crucial to prevent DDI with TKI.
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Availability of data and materials
All data generated or analysed during this study are included in this published article [and its supplementary information files].
Abbreviations
- ALP:
-
Alkaline phosphatase
- ALT:
-
ALanine transaminase
- AST:
-
ASpartate transaminase
- CRP:
-
C-reactive protein
- CT:
-
Chemotherapy
- CM:
-
Complementarymedicine
- DDI:
-
Drug–drug interactions
- IQR:
-
Interquartile range
- MR:
-
Medication reconciliation
- PPI:
-
Proton pump inhibitor
- STS:
-
Soft tissue sarcoma
- TKI:
-
Tyrosine kinase inhibitor
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Conception or design of the work: AB, IG, AJ, PBR, ATS. Data collection: AB, IG, SEM, ACP, CT, DB, AM, SDP, CV, JA, FG, PBR, ATS. Data analysis and interpretation; AB, IG, AJ, ATS, FG, BB, PBR. Drafting the article: AB, IG, AJ, SEM, ACP, CT, DB, AM, FG, BB, ATS, PBR. Critical revision of the article: AB, IG, AJ, SEM, ACP, CT, DB, AM, MV, RB, SDP, CV, JA, FG, BB, PBR, ATS. Final approval of the version to be published: AB, IG, AG, SEM, ACP, CT, DB, AM, MV, RB, SDP, CV, JA, FG, PBR, ATS.
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The studies involving human participants were reviewed and approved by Local ethical committee for oncology of Cochin Hospital (AP-HP), CARPEM, university of Paris, France (number:578AB88). The patients/participants provided their written informed consent to participate in this study. All methods were carried out in accordance with relevant guidelines and regulations.
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Bellesoeur, A., Gataa, I., Jouinot, A. et al. Prevalence of drug–drug interactions in sarcoma patients: key role of the pharmacist integration for toxicity risk management. Cancer Chemother Pharmacol 88, 741–751 (2021). https://doi.org/10.1007/s00280-021-04311-4
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DOI: https://doi.org/10.1007/s00280-021-04311-4