Abstract 440P
Background
Targeted therapy is emerging as the frontline of cancer treatment due to improved clinical outcomes and enhanced quality of life among cancer patients. However, treatments related to adverse events (AEs) of targeted therapy are associated with the outcome of cancer treatments. This study investigated the frequency and severity of adverse events in cancer patients who receive targeted therapy.
Methods
The study was conducted at a university hospital in northern Thailand, from January to June 2023. We performed a retrospective study concerning patients treated with targeted therapy including multikinase inhibitors, epidermal-growth factors (EGFR) inhibitors, anaplastic lymphoma kinase (ALK) inhibitors, cyclin-dependent kinases 4 and 6 (CDK4/6), immune checkpoint inhibitors (ICIs), mammalian target of rapamycin (mTOR) inhibitors, and phosphoinositide 3-kinases (PI3Ks) inhibitors. All adverse events were reported by pharmacists and confirmed by medical oncologists in electronic medical record (EMR) based on the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. Descriptive statistics were applied for reporting frequency of AEs.
Results
There are 136 cancer patients with targeted therapy. The majority of patients were female (58.1%) with mean age 64.0 ± 11.9 years old. Non-small cell lung cancer is the most common cancer (47.1%) followed by hepatocellular carcinoma (14.7%) and breast cancer (11%). The frequency of targeted therapy treatment was erlotinib (18.4%), ceritinib (18.4%), regorafenib (10.3%) and ribociclib (8.1%). Eighty-two patients (60.3%) reported AEs. The most AEs were grade 1-2 (64%). Skin rash was the most common AE (22.8%), subsequently with dry skin (16.9%) and diarrhea (14.7%). Six patients (4.4%) had grade 3 AEs including skin rash (0.7%), Hand foot skin reaction (0.7%), transaminitis (1.5%), and neutropenia (1.5%).
Conclusions
This study demonstrated the frequency of AEs among cancer patients with targeted therapy, the most common AEs included dermatological problems. Rarely severe AEs were reported. Health care providers will need to educate and monitor cancer patients to prevent and monuments AEs during targeted therapy treatment.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
193P - Impact of coronavirus disease 2019 on patients with unresectable hepatocellular carcinoma treated with atezolizumab/bevacizumab
Presenter: Hongjae Chon
Session: Poster Display
Resources:
Abstract
194P - Real-world outcomes of cadonilimab (PD-1/CTLA-4 bispecific antibody) plus chemotherapy as first-line treatment in advanced gastric (G) or gastroesophageal junction (GEJ) cancer with PD-L1 CPS≤5
Presenter: Qi Xu
Session: Poster Display
Resources:
Abstract
195P - Ferroptosis signatures in pancreatic ductal adenocarcinomas and their role in patient survival: A translational unsupervised clustering analysis
Presenter: Quoc-Huy Trinh
Session: Poster Display
Resources:
Abstract
196P - Clinical significance of circulating CD8+ and CD4+ T cell proliferation in advanced gastric cancer receiving first-line chemotherapy
Presenter: In-Ho Kim
Session: Poster Display
Resources:
Abstract
197P - Treatment patterns and clinical outcomes of patients with unresectable advanced or metastatic (UAM) gastric/gastroesophageal junction adenocarcinoma (GA/GEJA) in China: A multicenter real-world study
Presenter: Yanqiao Zhang
Session: Poster Display
Resources:
Abstract
198P - Effectiveness of lenvatinib in patients with unresectable hepatocellular carcinoma: A multicenter observational study in Japan
Presenter: Namiki Izumi
Session: Poster Display
Resources:
Abstract
199P - Efficacy of endostar in combination with concurrent chemoradiotherapy in patients with locally advanced squamous cell carcinoma of esophagus: A randomized, open-label, phase II trial
Presenter: Yuexiao Qi
Session: Poster Display
Resources:
Abstract
200P - Prognosis of patients with hepatocellular carcinoma treated with transarterial chemoembolization: Development and validation of the ALFP score
Presenter: Baocuo Gong
Session: Poster Display
Resources:
Abstract
201P - A phase II study of serplulimab (a programmed death-1 inhibitor) with or without HLX04 (a bevacizumab biosimilar) for the treatment of advanced hepatocellular carcinoma
Presenter: Zhenggang Ren
Session: Poster Display
Resources:
Abstract
202P - Comparison of liver injury after transcatheter arterial chemoembolization and hepatic arterial infusion chemotherapy for intermediate and advanced hepatocellular carcinoma
Presenter: Yongru Chen
Session: Poster Display
Resources:
Abstract