Key result
Higher dose intensity of pegylated liposomal doxorubicin significantly increased the risk of hand-foot syndrome (OR 1.831) compared to lower dose intensity in breast cancer patients.
Why the study?
Pegylated liposomal doxorubicin causes adverse reactions including hand-foot syndrome and oral mucositis that can impair function and interrupt chemotherapy, prompting an analysis of risk factors to provide early warning indicators.
What are the risk factors for hand-foot syndrome and oral mucositis in breast cancer patients receiving pegylated liposomal doxorubicin?
Observational (n=395)
No
What are the risk factors for hand-foot syndrome and oral mucositis in breast cancer patients receiving pegylated liposomal doxorubicin?
Increased dose intensity, decreased white blood cell counts, and a history of cholelithiasis are independent risk factors for concurrent hand-foot syndrome and oral mucositis in breast cancer patients treated with pegylated liposomal doxorubicin.
May inform dose intensity selection to limit hand-foot syndrome; leaves open optimal regimens in breast cancer.
Introduction: Doxorubicin (DOX) is a primary treatment for breast cancer (BC), but its widespread use is hindered by cardiotoxicity. Pegylated liposomal doxorubicin (PLD) has been developed to enhance the efficacy of DOX and mitigate its cardiotoxic effects. However, PLD is associated with adverse reactions (ADRs) such as hand-foot syndrome (HFS) and oral mucositis (OM), which have garnered significant attention. Although not life-threatening, HFS and OM can cause severe discomfort and functional impairment. Severe cases may necessitate a reduced PLD dose or even delay or interrupt chemotherapy, ultimately leading to decreased medication compliance. Here, we conduct an analysis of the risk factors associated with HFS and OM during the PLD chemotherapy regimen, thus providing early warning indicators for the potential occurrence of these adverse reactions in BC patients. Methods: In this study, a total of 395 BC patients receiving PLD chemotherapy were enrolled. Follow-up observations towards the baseline and clinical characteristics in these patients were exhibited. The evaluation of HFS and OM in these patients was also performed based on the Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0. Analysis of factors influencing simultaneous incidence of HFS and OM was executed using the univariate analysis and multivariate logistic regression analysis. Results: Dose intensity, history of cholelithiasis, ALT, AST, and Hb were identified as related risk factors for HFS. Dose intensity and reductions in white blood cell (WBC) counts were associated with the risk of OM. Furthermore, increased dose intensity, decreased WBC counts, and a history of cholelithiasis emerged as independent risk factors for the concurrent occurrence of HFS and OM. Discussion: This study investigated the various risk factors related to HFS, OM, and their combination in BC patients undergoing PLD chemotherapy, offering insights for the prevention and treatment of BC and other cancers.
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Quan et al. (2025) conducted an observational in Breast cancer (n=395). Pegylated liposomal doxorubicin dose intensity (35 mg/m2) vs. 30 mg/m2 dose intensity was evaluated on Incidence of Hand-Foot Syndrome (HFS) (OR 1.831, 95% CI 1.100-3.047, p=0.020). Higher dose intensity of pegylated liposomal doxorubicin significantly increased the risk of hand-foot syndrome (OR 1.831) compared to lower dose intensity in breast cancer patients.
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