Abstract 311P
Background
Chemotherapy is one of the fundamental treatments in cancer patients, which has significantly improved survival rate. Alongside positive effects, many side effects. One of major side effects of these drugs is hepatotoxicity, initially develops as fatty liver and hepatic steatosis, but progresses to liver failure if harmful factor persist. To determine prevalence of fatty liver in breast and gastrointestinal cancers during and after chemotherapy and to investigate some of its effective causes.
Methods
This longitudinal cohort study was performed breast or gastrointestinal cancer patients undergoing chemotherapy at the Oncology Clinic of Birjand University of Medical Sciences, 2016-2017. Before and after chemotherapy, the patients were evaluated by sonography for fatty liver. Data were imported into SPSS software version 19 and analyzed by Chi-Square (or Fisher Test) and McNemar at 5% significance level.
Results
A total of 152 patients were enrolled in the study, of whom 85 had breast cancer and 67 had gastrointestinal cancers. Most patients were in age group of 45-54 years old (48 cases, 31.6%). Mean body mass index (BMI) was 23.17 ± 4.52. Frequency of fatty liver before and after chemotherapy increased from 2% to 46.7% in all patients (p = 0.0001). Frequency of fatty liver after chemotherapy was significantly higher in females than males (34.7 and 52.4%, respectively, p=0.04). There was no significant relationship between chemotherapy induced fatty liver with age (p=0.9), BMI (p=0.17), history of diabetes mellitus (p=0.2), and metabolic syndrome presence (p=0.4). The highest frequency of fatty liver was observed in patients treated with AC-T, FOLFOX and ECF with 53.5%, 42.9% and 29.2%, respectively (p = 0.09).
Conclusions
Results showed that chemotherapy is associated with a significantly increased risk of fatty liver occurrence, which is higher in women than men. However, occurrence of fatty liver following chemotherapy, regardless of diabetes, metabolic syndrome or BMI, as well as age of the patients, can be expected in all scenarios.
Clinical trial identification
Legal entity responsible for the study
Dr. Payam Izadpanahi from Reza Radiotherapy Oncology Center (RROC).
Funding
Birjand University of Medical Sciences.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
434P - Pan-Canadian evidence-based, consensus-driven cancer treatment protocols/information for use at the point of care by medical oncologists? Is there a need?
Presenter: Kiran Virik
Session: e-Poster Display Session
435P - Hypnotics and risk of cancer: A meta-analysis of observational studies
Presenter: Tzu Rong Peng
Session: e-Poster Display Session
436P - Clinicopathological characteristics and outcomes of adolescent and young adult (AYA) melanoma: Results from an Asian perspective
Presenter: Wei Lin Goh
Session: e-Poster Display Session
437P - Long-term efficacy and toxicity outcome of adjuvant external beam radiotherapy for medullary thyroid cancer: A single institution cohort study
Presenter: Ka Man Cheung
Session: e-Poster Display Session
438P - Real-world data of relapse after adjuvant treatment (Tx) in high-risk melanoma
Presenter: Carolina Ortiz Velez
Session: e-Poster Display Session
439P - Immunohistochemical analysis of p53 and Ki-67 in glioblastoma (GBM) and their correlations with patient survival
Presenter: Paulo Luz
Session: e-Poster Display Session
440P - Blinded independent central review of oncology trials: The monitoring of readers' performance
Presenter: Hubert Beaumont
Session: e-Poster Display Session
441P - Influence of radiation therapy of patients with somatotropic pituitary adenomas depending on the age of patients
Presenter: Saodat Issaeva
Session: e-Poster Display Session
442P - Results from the registrational phase I/II ARROW trial of pralsetinib (BLU-667) in patients (pts) with advanced RET mutation-positive medullary thyroid cancer (RET+ MTC)
Presenter: Bhumsuk Keam
Session: e-Poster Display Session