| Literature DB >> 28353192 |
Yasunobu Sekiguchi1, Haruko Takizawa2, Tadaaki Inano3, Yasutaka Fukuda3, Mutsumi Wakabayashi2, Keiji Sugimoto2, Shigeki Tomita4, Hiroshi Izumi4, Noriko Nakamura5, Tomohiro Sawada5, Yasunori Ohta6, Norio Komatsu3, Masaaki Noguchi2.
Abstract
Three patients under hemodialysis (HD) with relapsed/refractory multiple myeloma (MM) were administered panobinostat/bortezomib/dexamethasone (FVD). Case 1: The patient was a 66-year-old male with BJP-κ. FVD was effective, but HD could not be discontinued. He developed Grade 3 adverse events (AEs), including nausea, dehydration, and fatigue, following the common terminology criteria for adverse events v4.0. FVD was discontinued after the third course, while HD was continued. Case 2: The patient was a 65-year-old female with IgG-λ + BJP-λ. Amyloidosis was complicated. The first course of FVD was effective, but HD could not be discontinued. She developed G2 AEs, including nausea and fatigue. The cardiac amyloidosis worsened, and she died of heart and renal failure. Case 3: The patient was a 79-year-old male with BJP-κ. FVD was effective, and the HD could be discontinued on day 12 of treatment. No AEs were noted. However, he declined continuation of the FVD and died of MM relapse and renal failure. We analyzed the pharmacokinetics of panobinostat. There were no correlations between dose level and blood level of panobinostat or between blood level, efficacy, and incidence of AEs. We additionally measured the rate of elimination of the drug by HD.Entities:
Keywords: Hemodialysis; Panobinostat/bortezomib/dexamethasone (FVD) therapy; Relapsed/refractory multiple myeloma; Renal failure
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Year: 2017 PMID: 28353192 DOI: 10.1007/s12185-017-2222-4
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490