TY - JOUR
T1 - Chemotherapy-induced peripheral neuropathy in children and adolescent cancer patients
AU - Tay, Nicolette
AU - Laakso, E. Liisa
AU - Schweitzer, Daniel
AU - Endersby, Raelene
AU - Vetter, Irina
AU - Starobova, Hana
N1 - Funding Information:
NT is supported by the Childhood Cancer Research Scholarship and the E.M.A and M.C Henker Postgraduate Medical Research Scholarship. RE is supported by a Cancer Council WA Research Fellowship (1129) and a BrainChild Fellowship from The Pirate Ship Foundation. IV is supported by a NHMRC Career Development fellowship (1162503). HS is supported by the Children’s Hospital Foundation Fellowship (PCC0012021). This work was supported by an Australian National Health and Medical Research Council Ideas Grant (1186835) and a Kids’ Cancer Project grant (IV and HS).
Publisher Copyright:
Copyright © 2022 Tay, Laakso, Schweitzer, Endersby, Vetter and Starobova.
PY - 2022/10/14
Y1 - 2022/10/14
N2 - Brain cancer and leukemia are the most common cancers diagnosed in the pediatric population and are often treated with lifesaving chemotherapy. However, chemotherapy causes severe adverse effects and chemotherapy-induced peripheral neuropathy (CIPN) is a major dose-limiting and debilitating side effect. CIPN can greatly impair quality of life and increases morbidity of pediatric patients with cancer, with the accompanying symptoms frequently remaining underdiagnosed. Little is known about the incidence of CIPN, its impact on the pediatric population, and the underlying pathophysiological mechanisms, as most existing information stems from studies in animal models or adult cancer patients. Herein, we aim to provide an understanding of CIPN in the pediatric population and focus on the 6 main substance groups that frequently cause CIPN, namely the vinca alkaloids (vincristine), platinum-based antineoplastics (cisplatin, carboplatin and oxaliplatin), taxanes (paclitaxel and docetaxel), epothilones (ixabepilone), proteasome inhibitors (bortezomib) and immunomodulatory drugs (thalidomide). We discuss the clinical manifestations, assessments and diagnostic tools, as well as risk factors, pathophysiological processes and current pharmacological and non-pharmacological approaches for the prevention and treatment of CIPN.
AB - Brain cancer and leukemia are the most common cancers diagnosed in the pediatric population and are often treated with lifesaving chemotherapy. However, chemotherapy causes severe adverse effects and chemotherapy-induced peripheral neuropathy (CIPN) is a major dose-limiting and debilitating side effect. CIPN can greatly impair quality of life and increases morbidity of pediatric patients with cancer, with the accompanying symptoms frequently remaining underdiagnosed. Little is known about the incidence of CIPN, its impact on the pediatric population, and the underlying pathophysiological mechanisms, as most existing information stems from studies in animal models or adult cancer patients. Herein, we aim to provide an understanding of CIPN in the pediatric population and focus on the 6 main substance groups that frequently cause CIPN, namely the vinca alkaloids (vincristine), platinum-based antineoplastics (cisplatin, carboplatin and oxaliplatin), taxanes (paclitaxel and docetaxel), epothilones (ixabepilone), proteasome inhibitors (bortezomib) and immunomodulatory drugs (thalidomide). We discuss the clinical manifestations, assessments and diagnostic tools, as well as risk factors, pathophysiological processes and current pharmacological and non-pharmacological approaches for the prevention and treatment of CIPN.
KW - chemotherapy-induced peripheral neuropathy
KW - CIPN mechanisms
KW - neuroinflammation
KW - pediatric cancer patients and survivors
KW - pharmacological and non-pharmacological treatment strategies
UR - http://www.scopus.com/inward/record.url?scp=85140844717&partnerID=8YFLogxK
U2 - 10.3389/fmolb.2022.1015746
DO - 10.3389/fmolb.2022.1015746
M3 - Review article
C2 - 36310587
AN - SCOPUS:85140844717
VL - 9
JO - Frontiers in molecular biosciences
JF - Frontiers in molecular biosciences
SN - 2296-889X
M1 - 1015746
ER -