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Risk factors for nausea and vomiting requiring the daily administration of 5-HT3 receptor antagonists in radiotherapy combined with temozolomide for high-grade glioma.
Takagi, Mai; Sagara, Atsunobu; Kumakura, Yasuo; Watanabe, Minako; Inoue, Rikako; Miyazaki, Masayuki; Ohka, Fumiharu; Motomura, Kazuya; Natsume, Atsushi; Wakabayashi, Toshihiko; Saito, Ryuta; Yamada, Kiyofumi.
Afiliação
  • Takagi M; Department of Hospital Pharmacy, Nagoya University Hospital, Nagoya, Japan.
  • Sagara A; Department of Hospital Pharmacy, Nagoya University Hospital, Nagoya, Japan.
  • Kumakura Y; Department of Hospital Pharmacy, Nagoya University Hospital, Nagoya, Japan.
  • Watanabe M; Department of Hospital Pharmacy, Nagoya University Hospital, Nagoya, Japan.
  • Inoue R; Department of Hospital Pharmacy, Nagoya University Hospital, Nagoya, Japan.
  • Miyazaki M; Department of Hospital Pharmacy, Nagoya University Hospital, Nagoya, Japan.
  • Ohka F; Department of Neurosurgery, Nagoya University Hospital, Nagoya, Japan.
  • Motomura K; Department of Neurosurgery, Nagoya University Hospital, Nagoya, Japan.
  • Natsume A; Department of Neurosurgery, Nagoya University Hospital, Nagoya, Japan.
  • Wakabayashi T; Department of Neurosurgery, Nagoya University Hospital, Nagoya, Japan.
  • Saito R; Department of Neurosurgery, Nagoya University Hospital, Nagoya, Japan.
  • Yamada K; Department of Hospital Pharmacy, Nagoya University Hospital, Nagoya, Japan.
Nagoya J Med Sci ; 86(2): 304-313, 2024 May.
Article em En | MEDLINE | ID: mdl-38962412
ABSTRACT
Radiotherapy combined with temozolomide (TMZ+RT) is the primary treatment for high-grade glioma. TMZ is classified as a moderate emetic risk agent and, thus, supportive care for nausea and vomiting is important. In Nagoya University Hospital, all patients are treated with a 5-hydroxy-tryptamine 3 receptor antagonist (5-HT3RA) for the first 3 days. The daily administration of 5-HT3RA is resumed after the 4th day based on the condition of patients during TMZ+RT. Therefore, the present study investigated risk factors for nausea and vomiting in patients requiring the daily administration of 5-HT3RA. Patients with high-grade glioma who received TMZ+RT between January 2014 and December 2019 at our hospital were included. Patients were divided into two groups a control group (patients who did not resume 5-HT3RA) and resuming 5-HT3RA group (patients who resumed 5-HT3RA after the 4th day), and both groups were compared to identify risk factors for nausea and vomiting during TMZ+RT. There were 78 patients in the control group (68%) and 36 in the resuming 5-HT3RA group (32%). A multivariate analysis of patient backgrounds in the two groups identified age <18 years, PS 2 or more, and occipital lobe tumors as risk factors for nausea and vomiting. Nausea and vomiting were attenuated in 30 patients (83%) in the resuming 5-HT3RA group following the resumption of 5-HT3RA. The results obtained highlight the importance of extracting patients with these risk factors before the initiation of therapy and the early resumption or daily administration of 5-HT3RA according to the condition of each patient.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vômito / Antagonistas do Receptor 5-HT3 de Serotonina / Temozolomida / Glioma / Náusea Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vômito / Antagonistas do Receptor 5-HT3 de Serotonina / Temozolomida / Glioma / Náusea Idioma: En Ano de publicação: 2024 Tipo de documento: Article