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Clinical interaction between dexamethasone and aprepitant in chemotherapy for lymphoma.
Hatano, Kaoru; Fujiwara, Shin-Ichiro; Umino, Kento; Ikeda, Takashi; Nakano, Hirofumi; Mashima, Kiyomi; Kawaguchi, Shin-Ichiro; Ito, Shoko; Toda, Yumiko; Nagayama, Takashi; Minakata, Daisuke; Yamasaki, Ryoko; Morita, Kaoru; Yamamoto, Chihiro; Ashizawa, Masahiro; Sato, Kazuya; Ueda, Masuzu; Ohmine, Ken; Kanda, Yoshinobu.
Affiliation
  • Hatano K; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Fujiwara SI; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Umino K; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Ikeda T; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Nakano H; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Mashima K; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Kawaguchi SI; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Ito S; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Toda Y; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Nagayama T; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Minakata D; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Yamasaki R; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Morita K; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Yamamoto C; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Ashizawa M; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Sato K; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Ueda M; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Ohmine K; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan.
  • Kanda Y; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotuke City, Tochigi, 329-0498, Japan. ycanda-tky@umin.ac.jp.
Ann Hematol ; 101(6): 1211-1216, 2022 Jun.
Article in En | MEDLINE | ID: mdl-35403851
ABSTRACT
Aprepitant (Apr) is an effective antiemetic agent for chemotherapy-induced nausea and vomiting (CINV). Current CINV guidelines recommend the antiemetic combination of a 5-HT3 receptor antagonist, Apr, and dexamethasone (Dex) for highly emetogenic chemotherapies. Apr inhibits CYP3A4 dose-dependently. Since Dex is metabolized by CYP3A4, the combined use of Apr and Dex inhibits Dex metabolism. CINV guidelines therefore recommend dose-reduction of Dex when Apr and Dex are used together. However, there is some controversy over whether or not Dex should be reduced when administered as an antitumor agent for lymphoid malignancies. We retrospectively compared the antitumor effect of Dex-containing chemotherapy in which Dex is administered at the usual dose without Apr (group A) or administered at a half-dose in combination with Apr (group B). We analyzed 62 consecutive patients with refractory or relapsed CD20 + B cell lymphoma who received R-DHAP therapy in our hospital, including 29 and 33 cases in groups A and B, respectively. The response rate at the end of the first course of R-DHAP was 62.1% and 54.5%, respectively (P = 0.61). As another endpoint to evaluate the effect of Dex, group B tended to show greater suppression of the lymphocyte count (P = 0.05). Therefore, decreasing the dose of Dex by half appeared to be reasonable when combined with Apr.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma / Antiemetics / Antineoplastic Agents Type of study: Guideline / Observational_studies Limits: Humans Language: En Journal: Ann Hematol Journal subject: HEMATOLOGIA Year: 2022 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma / Antiemetics / Antineoplastic Agents Type of study: Guideline / Observational_studies Limits: Humans Language: En Journal: Ann Hematol Journal subject: HEMATOLOGIA Year: 2022 Document type: Article Affiliation country: Japan