tetano
Editor, Senior Moderator
Antiviral Res
. 2024 Feb 29:224:105853.
doi: 10.1016/j.antiviral.2024.105853. Online ahead of print. Virological and clinical outcomes in outpatients treated with baloxavir or neuraminidase inhibitors for A(H3N2) influenza: A multicenter study of the 2022-2023 season
Takeyuki Goto[SUP] 1 [/SUP], Naoki Kawai[SUP] 2 [/SUP], Takuma Bando[SUP] 3 [/SUP], Yoshio Takasaki[SUP] 4 [/SUP], Shizuo Shindo[SUP] 5 [/SUP], Naoki Tani[SUP] 6 [/SUP], Yong Chong[SUP] 7 [/SUP], Hideyuki Ikematsu[SUP] 8 [/SUP]
Affiliations
While clinical trials have illuminated both the virological and clinical efficacy of baloxavir for influenza and post-treatment viral resistance, these aspects warrant further study in real-world settings. In response, we executed a prospective, observational study of the Japanese 2022-2023 influenza season. A cohort of 73 A(H3N2)-diagnosed outpatients-36 treated with baloxavir, 20 with oseltamivir, and 17 with other neuraminidase inhibitors (NAIs)-were analyzed. Viral samples were collected before and after administering an antiviral on days 1, 5, and 10, respectively. Cultured viruses were amplified using RT-PCR and sequenced to detect mutations. Fever and other symptoms were tracked via self-reporting diaries. In the baloxavir cohort, viral detection was 11.1% (4/36) and 0% (0/36) on day 5 and day 10, respectively. Two isolates from day 5 (5.6%, 2/36) manifested I38T/M-substitutions in the polymerase acidic protein (PA). For oseltamivir and other NAIs, viral detection rates were 60.0% (12/20) and 52.9% (9/17) on day 5, and 16.7% (3/18) and 6.3% (1/16) on day 10, respectively. No oseltamivir-resistant neuraminidase mutations were identified after treatment. Median fever durations for the baloxavir, oseltamivir, and other NAI cohorts were 27.0, 38.0, and 36.0 h, respectively, with no significant difference. Two patients harboring PA I38T/M-substitutions did not exhibit prolonged fever or other symptoms. These findings affirm baloxavir's virological and clinical effectiveness against A(H3N2) in the 2022-2023 season and suggest limited clinical influence of post-treatment resistance emergence.
Keywords: Baloxavir; Clinical setting; Influenza; Oseltamivir; Variant.
. 2024 Feb 29:224:105853.
doi: 10.1016/j.antiviral.2024.105853. Online ahead of print. Virological and clinical outcomes in outpatients treated with baloxavir or neuraminidase inhibitors for A(H3N2) influenza: A multicenter study of the 2022-2023 season
Takeyuki Goto[SUP] 1 [/SUP], Naoki Kawai[SUP] 2 [/SUP], Takuma Bando[SUP] 3 [/SUP], Yoshio Takasaki[SUP] 4 [/SUP], Shizuo Shindo[SUP] 5 [/SUP], Naoki Tani[SUP] 6 [/SUP], Yong Chong[SUP] 7 [/SUP], Hideyuki Ikematsu[SUP] 8 [/SUP]
Affiliations
- PMID: 38430970
- DOI: 10.1016/j.antiviral.2024.105853
While clinical trials have illuminated both the virological and clinical efficacy of baloxavir for influenza and post-treatment viral resistance, these aspects warrant further study in real-world settings. In response, we executed a prospective, observational study of the Japanese 2022-2023 influenza season. A cohort of 73 A(H3N2)-diagnosed outpatients-36 treated with baloxavir, 20 with oseltamivir, and 17 with other neuraminidase inhibitors (NAIs)-were analyzed. Viral samples were collected before and after administering an antiviral on days 1, 5, and 10, respectively. Cultured viruses were amplified using RT-PCR and sequenced to detect mutations. Fever and other symptoms were tracked via self-reporting diaries. In the baloxavir cohort, viral detection was 11.1% (4/36) and 0% (0/36) on day 5 and day 10, respectively. Two isolates from day 5 (5.6%, 2/36) manifested I38T/M-substitutions in the polymerase acidic protein (PA). For oseltamivir and other NAIs, viral detection rates were 60.0% (12/20) and 52.9% (9/17) on day 5, and 16.7% (3/18) and 6.3% (1/16) on day 10, respectively. No oseltamivir-resistant neuraminidase mutations were identified after treatment. Median fever durations for the baloxavir, oseltamivir, and other NAI cohorts were 27.0, 38.0, and 36.0 h, respectively, with no significant difference. Two patients harboring PA I38T/M-substitutions did not exhibit prolonged fever or other symptoms. These findings affirm baloxavir's virological and clinical effectiveness against A(H3N2) in the 2022-2023 season and suggest limited clinical influence of post-treatment resistance emergence.
Keywords: Baloxavir; Clinical setting; Influenza; Oseltamivir; Variant.