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Biol Pharm Bull ; 47(3): 692-697, 2024 Mar 25.
Article in English | MEDLINE | ID: mdl-38417893

ABSTRACT

Existing antiemetic therapy against emetic-risk agents across malignancies 24 h post-dose in the acute period in cisplatin (CDDP)-based regimens yields a satisfactory complete response (CR) rate of ≥90%. However, the control rate after 24 h in the delayed period is unsatisfactory. This study compared the efficacy of fosnetupitant (F-NTP), a neurokinin 1 receptor antagonist, with that of fosaprepitant (F-APR) and aprepitant (APR) in the treatment of patients with cancer at high emetic risk due to chemotherapy. In this retrospective case-control study involving patients receiving cisplatin-containing regimens and neurokinin 1 receptor antagonists, patients were divided into three groups based on prophylactic antiemetic therapy: F-NTP, F-APR, and APR. The CR rate was evaluated for each period up to 168 h and further subdivided into acute (0-24 h), delayed (24-120 h), overall (0-120 h), and beyond-delayed (120-168 h) periods. Eighty-eight patients were included in the F-NTP group, 66 in the F-APR group, and 268 in the APR group. The CR rates at 0-168 and 120-168 h after cisplatin administration were significantly higher in the F-NTP group than in the F-APR and APR groups. After adjusting for confounding factors, F-NTP use was an independent factor in the multivariate analysis. Prophylactic antiemetic therapy, including F-NTP, was effective and well-tolerated during the delayed period. The efficacy of F-NTP in managing chemotherapy-induced nausea and vomiting was superior to those of F-APR and APR during the study period.


Subject(s)
Antiemetics , Antineoplastic Agents , Morpholines , Neoplasms , Humans , Aprepitant/therapeutic use , Cisplatin/adverse effects , Emetics/adverse effects , Retrospective Studies , Case-Control Studies , Vomiting/chemically induced , Vomiting/prevention & control , Vomiting/drug therapy , Neurokinin-1 Receptor Antagonists/therapeutic use , Neurokinin-1 Receptor Antagonists/pharmacology , Neoplasms/drug therapy , Gastrointestinal Agents/therapeutic use , Antineoplastic Agents/adverse effects
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