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Clinical pharmacokinetics of oxaliplatin in a hemodialysis patient with advanced gastric cancer.
Maruta, Motofumi; Miyoshi, Takanori; Matsuo, Naomi; Yamashina, Takuya; Irie, Kenji; Tsuruta, Minako; Tsukada, Hiroko; Tsuruyama, Moeko; Nagano, Masahisa; Hiraki, Yoichi.
Affiliation
  • Maruta M; Department of Pharmacy, National Hospital Organization Beppu Medical Center, Oita, Japan.
  • Miyoshi T; Department of Pharmacy, National Hospital Organization Beppu Medical Center, Oita, Japan.
  • Matsuo N; Department of Pharmacy, National Hospital Organization Beppu Medical Center, Oita, Japan.
  • Yamashina T; Department of Pharmacy, National Hospital Organization Beppu Medical Center, Oita, Japan.
  • Irie K; Department of Pharmacy, National Hospital Organization Beppu Medical Center, Oita, Japan.
  • Tsuruta M; Department of Pharmacy, National Hospital Organization Beppu Medical Center, Oita, Japan.
  • Tsukada H; Department of Pharmacy, National Hospital Organization Beppu Medical Center, Oita, Japan.
  • Tsuruyama M; Department of Pharmacy, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.
  • Nagano M; Department of Pharmacy, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.
  • Hiraki Y; Department of Pharmacy, National Hospital Organization Beppu Medical Center, Oita, Japan.
J Chemother ; 33(1): 51-55, 2021 Feb.
Article in En | MEDLINE | ID: mdl-32066346
We administered FOLFOX (oxaliplatin (L-OHP) plus infusional 5-fluorouracil (5-FU) and leucovorin) to an hemodialysis (HD) patient with advanced gastric cancer (AGC), and investigated pharmacokinetics (PKs) and dialyzability of L-OHP. The patient was a 54-year-old Japanese man with a diagnosis of inoperable AGC. FOLFOX was instituted 3 h prior to the start of a 4 h HD period with the L-OHP and 5-FU doses reduced by 50% for the first cycle, and 30% reduced dose was administered for the second cycle. We performed an analysis of the PKs of L-OHP during these two cycles. Volume of distribution and area under the curve of the 30% reduced L-OHP dose were 56.7 L and 30.0 µg·h/mL, respectively. A dose reduction of L-OHP by 30%-50% may be advisable for the initial administration, given the need for careful administration of chemotherapy in HD patients, with particular attention to the development of hematological toxicities and neuropathy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stomach Neoplasms / Renal Dialysis / Oxaliplatin / Kidney Failure, Chronic Type of study: Prognostic_studies Limits: Humans / Male / Middle aged Language: En Journal: J Chemother Journal subject: ANTINEOPLASICOS / TERAPIA POR MEDICAMENTOS Year: 2021 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stomach Neoplasms / Renal Dialysis / Oxaliplatin / Kidney Failure, Chronic Type of study: Prognostic_studies Limits: Humans / Male / Middle aged Language: En Journal: J Chemother Journal subject: ANTINEOPLASICOS / TERAPIA POR MEDICAMENTOS Year: 2021 Document type: Article Affiliation country: Country of publication: