» Articles » PMID: 36505840

Safety Profile of Tyrosine Kinase Inhibitors Used in Non-small-cell Lung Cancer: An Analysis from the Italian Pharmacovigilance Database

Overview
Journal Front Oncol
Specialty Oncology
Date 2022 Dec 12
PMID 36505840
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: Non-small cell lung cancer (NSCLC) is often caused by molecular alterations that can be detected by predictive biomarkers including mutations or amplifications of several genes. Several tyrosine kinase inhibitors (TKIs) have been approved in Europe by the European Medicines Agency (EMA) for NSCLC. The aim of this study was to analyze the onset of adverse drug reactions (ADRs) related to TKIs in NSCLC through a spontaneous reporting system (SRS) database.

Methods: All ADR reports having as suspected drug afatinib (AFT), alectinib (ALEC), brigatinib (BRG), ceritinib (CER), crizotinib (CRIZ), erlotinib (ERL), gefitinib (GEF), lorlatinib (LORL), nintedanib (NTB), and osimertinib (OSI) recorded into the Report Reazioni Avverse dei Medicinali (RAM) system database for national data and into the Italian SRS database for Sicilian data and collected from 2006 to 2021 have been evaluated. A descriptive analysis of basal demographic and drug-related characteristics was performed. A case-by-case methodology was conducted paying particular attention to all serious ADR reports collected in Sicily, focusing on type of seriousness, age, sex, concomitant drugs, and comorbidities.

Results: Of the 3,048 Italian reports, most of ADRs were related to ERL ( = 1,448), followed by AFT ( = 435) and GEF ( = 366). ADR reports were slightly more frequent in females (52.2%) and in the age group >65 years (53.0%). A higher number of cases were related to skin disorders ( = 1,766; 57.9%), followed by gastrointestinal disorders ( = 1,024; 33.6%), general disorders and administration site conditions (n = 536; 17.6%), and infections ( = 483; 15.8%). The case-by-case assessment of Sicilian ADRs showed that 33 cases were serious (12.5%) and mainly involved ERL ( = 17; 51.5%), occurring in males with a higher onset of respiratory diseases (30.3%) such as respiratory failure, interstitial lung disease and dyspnea.

Discussion: The analysis of spontaneous ADR reports of TKIs confirmed, in general, well-known risks, which often include skin, gastrointestinal, general, liver, and respiratory diseases as well as infections. However, more attention should be paid to the occurrence of serious life-threatening ADRs including respiratory failure, interstitial lung disease, and cardiogenic shock, especially in young patients.

Citing Articles

Neuropsychiatric Adverse Events with Monoclonal Antibodies Approved for Multiple Myeloma: An Analysis from the FDA Adverse Event Reporting System.

Cicala G, Russo G, Santoro V, Franchina T, Silvestris N, Santarpia M Pharmaceuticals (Basel). 2024; 17(10).

PMID: 39458907 PMC: 11510275. DOI: 10.3390/ph17101266.


Clinical characteristics and influencing factors of anti-PD-1/PD-L1-related severe cardiac adverse event: based on FAERS and TCGA databases.

Cheng X, Lin J, Wang B, Huang S, Liu M, Yang J Sci Rep. 2024; 14(1):22199.

PMID: 39333574 PMC: 11436968. DOI: 10.1038/s41598-024-72864-4.


Real-world evidence of brigatinib as second-line treatment after crizotinib for ALK+ non-small cell lung cancer using South Korean claims data (K-AREAL).

Lee J, Nam J, Kwon S, Kim B, Ha S Cancer Med. 2024; 13(14):e70030.

PMID: 39030811 PMC: 11257998. DOI: 10.1002/cam4.70030.


Osimertinib‑induced erythromelalgia: A case report.

Bolzon A, Alessia Guidotti A, Alaibac M Exp Ther Med. 2024; 28(1):273.

PMID: 38800043 PMC: 11117111. DOI: 10.3892/etm.2024.12561.


Thromboembolic Events Associated with Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors: A Pharmacovigilance Analysis of the US FDA Adverse Event Reporting System (FAERS) Database.

Yang X, Yang B, Li D, Pan W, Tong Q, Wang L Clin Drug Investig. 2024; 44(3):199-207.

PMID: 38376794 DOI: 10.1007/s40261-024-01346-2.


References
1.
Harandi A, Zaidi A, Stocker A, Laber D . Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers. J Oncol. 2009; 2009:567486. PMC: 2677718. DOI: 10.1155/2009/567486. View

2.
Rothenstein J, Letarte N . Managing treatment-related adverse events associated with Alk inhibitors. Curr Oncol. 2014; 21(1):19-26. PMC: 3921027. DOI: 10.3747/co.21.1740. View

3.
Seidman J, Eichenfield D, Orme C . Nevoid melanoma and eruptive nevi from erlotinib. Dermatol Online J. 2020; 26(6). View

4.
Soria J, Ohe Y, Vansteenkiste J, Reungwetwattana T, Chewaskulyong B, Lee K . Osimertinib in Untreated EGFR-Mutated Advanced Non-Small-Cell Lung Cancer. N Engl J Med. 2017; 378(2):113-125. DOI: 10.1056/NEJMoa1713137. View

5.
Hong S, An H, Kim K, Lee S, Lee Y, Yuh Y . Impact of Epidermal Growth Factor Receptor Mutation on Clinical Outcomes of Nintedanib Plus Docetaxel in Patients with Previously Treated Non-Small Cell Lung Cancer from the Korean Named Patient Program. Oncology. 2018; 96(1):51-58. DOI: 10.1159/000492472. View