Abstract 3117
Background
Cancer patients undergoing chemotherapy experienced many adverse effects. The purpose of this study was to assess the symptoms were experienced by cancer patients using the Edmonton Symptom Assessment scale.
Methods
The study was cross-sectional and was conducted in one-day clinic in large oncology hospital in capital of Greece. The sample consisted of 199 cancer patients undergoing chemotherapy in cycle 3. Date was collected using Edmonton Symptom Assessment Scale (ESAS) additionally with a questionnaire for demographic and clinical characteristics, Descriptive and conductive statistical methods were used.
Results
The vast majority of patients were women (n = 153, 76.9%) and had breast cancer (n = 153, 76,9%). Patients experienced mild severity symptoms as could be seen from the mean values of symptoms (physical symptoms: 14.85±10.25, emotional symptoms: 6.84±5.24, well-being 3.73±2.61). There is a statistically significant difference between type of cancer and shortness of breath (p = 0.015) between gender and nausea (p = 0.013) gender and shortness of breath (p = 0.013). In addition, there is statistically difference between drowsiness and how is chemotherapy given (p = 0.0017). The rest of the comparisons revealed that there is a statistical significant difference between pain and type of chemotherapy regimen (p = 0.014), nausea and type of chemotherapy regimen (p = 0.012), well-being and type of chemotherapy regimen (p = 0.003) as well as between total symptoms and type of chemotherapy regimen (p = 0.025).
Conclusions
Edmonton Symptom Assessment Scale was an important clinical instrument for assessing symptoms in clinical practice. There is a need for further research in order to use this tool in a daily clinical practice in one day chemotherapy clinic.
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
2108 - Biomarker analyses of ramucirumab in patients with platinum refractory urothelial cancer from RANGE, a global, randomized, double-blind, phase 3 study.
Presenter: Michiel Van der Heijden
Session: Poster Display session 3
Resources:
Abstract
3090 - Comparison of Immuno-Oncology (IO) Biomarkers in Adenocarcinoma (ACB), Urothelial Carcinoma (UCB) and Squamous Cell Carcinoma (SCCB) of the Bladder, with interim results from PURE01
Presenter: Daniele Raggi
Session: Poster Display session 3
Resources:
Abstract
5211 - Potential role of a clinical, taxonomical classification and RNA expression integrated signature to predict response to neoadjuvant platinum-based chemotherapy in muscle-invasive bladder cancer (MIBC) patients
Presenter: Albert Font
Session: Poster Display session 3
Resources:
Abstract
3206 - Hyperphosphatemia due to Erdafitinib (a Pan-FGFR Inhibitor) and Anti-tumor Activity Among Patients (Pts) with Advanced Urothelial Carcinoma (UC)
Presenter: Scott Tagawa
Session: Poster Display session 3
Resources:
Abstract
3110 - Prognostic role of FGFR Mutations and FGFR mRNA expression in metastatic urothelial cancer treated with anti-PD(L1) inhibitors in first and second line setting
Presenter: Florian Roghmann
Session: Poster Display session 3
Resources:
Abstract
3564 - Circulating tumour DNA (ctDNA) utility as a biomarker for metastatic urothelial carcinoma (mUC)
Presenter: Jean-Michel Lavoie
Session: Poster Display session 3
Resources:
Abstract
2760 - Comparative analysis of tumor mutational burden (TMB) prediction methods and its association with determinants of the tumor immune microenvironment of urothelial bladder cancer (UBC)
Presenter: Markus Eckstein
Session: Poster Display session 3
Resources:
Abstract
2513 - The Immunoscore in patients with urothelial carcinoma treated with neoadjuvant chemotherapy: clinical significance for pathological response and survival
Presenter: Elise Nassif
Session: Poster Display session 3
Resources:
Abstract
2835 - Genomic analysis of urothelial cancer and associations with treatment choice and outcome
Presenter: David Sarid
Session: Poster Display session 3
Resources:
Abstract
5763 - cfDNA is an acceptable but insufficient means of characterizing FGFR3 mutation in patients with metastatic urothelial cancer (mUC)
Presenter: Sumanta Pal
Session: Poster Display session 3
Resources:
Abstract