Highlights
- •Encephalopathy and leukoencephalopathy are the commonest clinico-radiologic features of capecitabine-related neurotoxicity.
- •Capecitabine-related neurotoxicity preponderated amongst females, but the clinico-radiologic features were similar in both genders.
- •Prognosis is excellent, and early recognition of neurotoxic symptoms and early cessation of capecitabine are important.
Abstract
Aim
To study the clinical and radiologic features of patients with capecitabine neurotoxicity.
Methods
We performed a retrospective analysis and systematic review on the clinical and radiologic
characteristics of all patients with capecitabine neurotoxicity reported in literature
between 2003 and 2020.
Results
24 cases including our patient were retrospectively analysed, with their clinical
and radiologic features summarized. Their median age was 59 years old (ranges from
31 to 82 years old). Encephalopathy was the predominant clinical symptom affecting
more than half (15/24, 63%) of the patients. This was followed by cerebellar ataxia
(10/24, 42%). Amongst the patients who had magnetic resonance imaging(MRI) brain imaging
performed, majority of them (18/23, 78%) had acute radiologic abnormalities. Leukoencephalopathy
was the commonest radiologic abnormality seen in more than half of the patients (15/23,65%).
Despite the preponderance of female patients in our study, there were no significant
statistical differences in the clinical and radiologic features. Short term prognosis
was excellent with complete resolution of neurologic symptoms observed in nearly all
of the patients (22/23, 96%).
Conclusion
Capecitabine-related neurotoxicity is an uncommon cause of toxic encephalopathy, with
a predilection for females. Clinical features are non-specific, with encephalopathy
being the commonest. Prognosis remains good with timely recognition, and cessation
of capecitabine. Future research looking into other pathogenic pharmacogenetic processes
should be conducted for further elucidation of these associations.
Keywords
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Article info
Publication history
Published online: September 30, 2022
Accepted:
September 27,
2022
Received in revised form:
September 27,
2022
Received:
July 11,
2022
Identification
Copyright
© 2022 Elsevier B.V. All rights reserved.