Loading…

How Asian Breast Cancer Patients Experience Unequal Incidence of Chemotherapy Side Effects: A Look at Ethnic Disparities in Febrile Neutropenia Rates

The majority of published findings on chemotherapy-induced febrile neutropenia (FN) are restricted to three ethnic groups: Asians, Caucasians, and African Americans. In this two-part study, we examined FN incidence and risk factors in Chinese, Malay, and Indian chemotherapy-treated breast cancer (BC...

Full description

Saved in:
Bibliographic Details
Published in:Cancers 2023-07, Vol.15 (14), p.3590
Main Authors: Lim, Zi Lin, Ho, Peh Joo, Hartman, Mikael, Tan, Ern Yu, Riza, Nur Khaliesah Binte Mohamed, Lim, Elaine Hsuen, Nitar, Phyu, Joint Breast Cancer Registry Jbcr, Wong, Fuh Yong, Li, Jingmei
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The majority of published findings on chemotherapy-induced febrile neutropenia (FN) are restricted to three ethnic groups: Asians, Caucasians, and African Americans. In this two-part study, we examined FN incidence and risk factors in Chinese, Malay, and Indian chemotherapy-treated breast cancer (BC) patients. Hospital records or ICD codes were used to identify patients with FN. In both the Singapore Breast Cancer Cohort (SGBCC) and the Joint Breast Cancer Registry (JBCR), the time of the first FN from the start of chemotherapy was estimated using Cox regression. Multinomial regression was used to evaluate differences in various characteristics across ethnicities. FN was observed in 170 of 1014 patients in SGBCC. The Cox model showed that non-Chinese were at higher risk of developing FN (HR [95% CI]:2.04 [1.44-2.88], < 0.001; HR :1.88 [1.11-3.18], = 0.018). In JBCR, FN was observed in 965 of 7449 patients. Univariable Cox models identified ethnicity, a lower baseline absolute neutrophil count, non-luminal A proxy subtypes, and anthracycline-containing regimens as risk factors. Disparities across ethnicities' risk (HR :1.29 [1.07-1.54], = 0.006; HR :1.50 [1.19-1.88], < 0.001) remained significant even after further adjustments. Finally, an age-adjusted multinomial model showed that Malays ( 0.006) and Indians ( = 0.009) were significantly more likely to develop multiple episodes of FN during treatment. Ethnic differences in chemotherapy-induced FN among BC patients exist. Further studies can focus on investigating pharmacogenetic differences across ethnicities.
ISSN:2072-6694
2072-6694
DOI:10.3390/cancers15143590