| Literature DB >> 31695003 |
Riku Nagao1,2, Rika Hosoba2, Yuichi Yahagi1, Tadahiro Gunji2, Hideki Uryu2, Daiki Hattori2, Mamiko Momoki1,2, Hiroyuki Yamazaki1.
Abstract
We report a 55-year-old man who began undergoing hemodialysis for polycystic kidney disease 17 years ago. Because pancytopenia and susceptibility to infection were identified, a bone marrow biopsy was performed, resulting in a diagnosis of acute promyelocytic leukemia (APL). All-trans retinoic acid (ATRA) treatment was initiated, but promyelocytic leukemia/retinoic acid receptor alpha gene fusion without remission was identified by fluorescence in situ hybridization. We administered ATRA/arsenic trioxide (ATO) combination therapy for therapy-resistant APL and confirmed molecular genetic remission. The ATRA/ATO combination therapy was continued, obtaining complete remission 2 years after commencement of treatment. Cystic infections continued during ATRA/ATO combination therapy, similar to infections before APL morbidity, and there were no adverse events leading to treatment discontinuation. ATRA/ATO combination therapy is considered a safe and effective treatment for therapy-resistant APL patients on hemodialysis.Entities:
Keywords: Acute promyelocytic leukemia; All-trans retinoic acid; Arsenic trioxide; Dialysis
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Year: 2019 PMID: 31695003 DOI: 10.11406/rinketsu.60.1431
Source DB: PubMed Journal: Rinsho Ketsueki ISSN: 0485-1439