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All-Trans Retinoic Acid-Induced Ototoxicity during Chemotherapy in Pediatric Acute Promyelocytic Leukemia

Bibliographic Data

ID15719787
AuthorsJong‐Hyeon Lee (0000-0002-9090-2192, Yeungnam University Medical Center, corresponding author), Jong Hyeon Lee (Department of Pediatrics, Yeungnam University Medical Center, Daegu 42415, Korea), Jong Ho Lee (0000-0002-2724-7295, Yeungnam University Medical Center), Jae Min Lee (0000-0002-0479-2282, Yeungnam University Medical Center)
Year2021
Volume8
Issue1
Pages27-27
Publication date2021-01-06
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children8010027
PMID33419229
OpenAlexW3118818548
LanguageEN
References cited11

All-trans retinoic acid (ATRA) is known to induce complete remission of acute promyelocytic leukemia (APL) and its use has significantly improved the cure rate of APL. However, ATRA also causes side effects such as differentiation syndrome or intracranial hypertension. In our case, the patient was diagnosed with APL and developed hearing loss thrice while being treated with ATRA. Therefore, we reduced the dose of ATRA instead of stopping it altogether and administered dexamethasone to the patient. A hearing test performed thereafter revealed recovery of hearing. No recurrence of hearing loss occurred after prednisolone and ATRA were combined in the maintenance phase. In conclusion, ATRA-associated hearing loss is reversible, and it is not necessary to stop ATRA. We recommend completion of a randomized clinical trial using dexamethasone in combination with ATRA to prevent hearing loss caused by ATRA

Acute promyelocytic leukemia · Audiology · Chemotherapy · Dexamethasone · Hearing loss · Ototoxicity · Prednisolone · Retinoic acid · Side effect (computer science · Tretinoin · Acute Myeloid Leukemia Research · Chemistry · Glioma Diagnosis and Treatment · Medicine · Retinoids in leukemia and cellular processes · Biochemistry · Gastroenterology · Internal Medicine · Oncology

Citation velocityhistorical
Highly citedNo

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