TY - JOUR
T1 - Ifosfamide-induced nephrotoxicity in oncological patients
AU - Quiroz-Aldave, Juan Eduardo
AU - Durand-Vásquez, María Del Carmen
AU - Chávez-Vásquez, Freddy Shanner
AU - Rodríguez-Angulo, Alexandra Noelia
AU - Gonzáles-Saldaña, Sonia Elizabeth
AU - Alcalde-Loyola, Carlos César
AU - Coronado-Arroyo, Julia Cristina
AU - Zavaleta-Gutiérrez, Francisca Elena
AU - Concepción-Urteaga, Luis Alberto
AU - Haro-Varas, Juan Carlos
AU - Concepción-Zavaleta, Marcio José
N1 - Publisher Copyright:
© 2023 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2024
Y1 - 2024
N2 - Introduction: Ifosfamide is an alkylating chemotherapeutic agent used in the treatment of various neoplasms. Its main adverse effects include renal damage. Areas covered: A comprehensive review was conducted, including 100 articles from the Scielo, Scopus, and EMBASE databases. Ifosfamide-induced nephrotoxicity is attributed to its toxic metabolites, such as acrolein and chloroacetaldehyde, which cause mitochondrial damage and oxidative stress in renal tubular cells. Literature review found a 29-year average age with no gender predominance and a mortality of 13%. Currently, no fully effective strategy exists for preventing ifosfamide-induced nephrotoxicity; however, hydration, forced diuresis, and other interventions are employed to limit renal damage. Long-term renal function monitoring is essential for patients treated with ifosfamide. Expert opinion: Ifosfamide remains essential in neoplasm treatment, but nephrotoxicity, often compounded by coadministered drugs, poses diagnostic challenges. Preventive strategies are lacking, necessitating further research. Identifying timely risk factors can mitigate renal damage, and a multidisciplinary approach manages established nephrotoxicity. Emerging therapies may reduce ifosfamide induced nephrotoxicity.
AB - Introduction: Ifosfamide is an alkylating chemotherapeutic agent used in the treatment of various neoplasms. Its main adverse effects include renal damage. Areas covered: A comprehensive review was conducted, including 100 articles from the Scielo, Scopus, and EMBASE databases. Ifosfamide-induced nephrotoxicity is attributed to its toxic metabolites, such as acrolein and chloroacetaldehyde, which cause mitochondrial damage and oxidative stress in renal tubular cells. Literature review found a 29-year average age with no gender predominance and a mortality of 13%. Currently, no fully effective strategy exists for preventing ifosfamide-induced nephrotoxicity; however, hydration, forced diuresis, and other interventions are employed to limit renal damage. Long-term renal function monitoring is essential for patients treated with ifosfamide. Expert opinion: Ifosfamide remains essential in neoplasm treatment, but nephrotoxicity, often compounded by coadministered drugs, poses diagnostic challenges. Preventive strategies are lacking, necessitating further research. Identifying timely risk factors can mitigate renal damage, and a multidisciplinary approach manages established nephrotoxicity. Emerging therapies may reduce ifosfamide induced nephrotoxicity.
KW - Fanconi syndrome
KW - Ifosfamide
KW - drug-related side effects and adverse reactions
KW - neoplasms
KW - nephrogenic diabetes insipidus
UR - http://www.scopus.com/inward/record.url?scp=85178397918&partnerID=8YFLogxK
U2 - 10.1080/14737140.2023.2290196
DO - 10.1080/14737140.2023.2290196
M3 - Artículo
C2 - 38031874
AN - SCOPUS:85178397918
SN - 1473-7140
VL - 24
SP - 5
EP - 14
JO - Expert Review of Anticancer Therapy
JF - Expert Review of Anticancer Therapy
IS - 1-2
ER -