C609T Polymorphism of NADPH Quinone Oxidoreductase 1 Correlates Clinical Hematological Toxicities in Lung Cancer Patients Treated with Amrubicin

نویسندگان

  • Misato Nagata
  • Tatsuo Kimura
  • Tomohiro Suzumura
  • Yukimi Kira
  • Toshiyuki Nakai
  • Kanako Umekawa
  • Hidenori Tanaka
  • Kuniomi Matsuura
  • Shigeki Mitsuoka
  • Naruo Yoshimura
  • Takako Oka
  • Shinzoh Kudoh
  • Kazuto Hirata
چکیده

BACKGROUND Amrubicin hydrochloride (AMR) is a key agent for lung cancer. NADPH quinone oxidoreductase 1 (NQO1) metabolizes the quinone structures contained in both amrubicin (AMR) and amrubicinol (AMR-OH). We hypothesized that NQO1 C609T polymorphism may affect AMR-related pharmacokinetics and clinical outcomes. METHODS Patients received AMR doses of 30 or 40 mg/m(2)/day on days 1-3. Plasma sampling was performed 24 hours after the first and third AMR injections. Concentrations of AMR and AMR-OH were determined by HPLC and the NQO1 C609T polymorphism was assayed by RT-PCR. RESULTS A total of 35 patients were enrolled. At a dose of 40 mg/m(2), the T/T genotype exhibited a tendency toward a relationship with decrease concentrations of AMR-OH on days 2 and 4. The genotype also showed a significant decrease of hematological toxicities (P < 0.05). CONCLUSIONS NQO1 C609T polymorphism had a tendency of correlation with the plasma concentrations of AMR-OH, and thereby had significant correlations with hematologic toxicities.

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عنوان ژورنال:

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2013