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Clinical interaction between dexamethasone and aprepitant in chemotherapy for lymphoma.

Kaoru HatanoShin-Ichiro FujiwaraKento UminoTakashi IkedaHirofumi NakanoKiyomi MashimaShin-Ichiro KawaguchiShoko ItoYumiko TodaTakashi NagayamaDaisuke MinakataRyoko YamasakiKaoru MoritaChihiro YamamotoMasahiro AshizawaKazuya SatoMasuzu UedaKen OhmineYoshinobu Kanda
Published in: Annals of hematology (2022)
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.
Keyphrases
  • chemotherapy induced
  • diffuse large b cell lymphoma
  • high dose
  • stem cells
  • acute lymphoblastic leukemia
  • clinical practice
  • peripheral blood
  • squamous cell carcinoma
  • bone marrow
  • smoking cessation