Corrigendum to ‘IMscin001 Part 2: a randomised phase III, open-label, multicentre study examining the pharmacokinetics, efficacy, immunogenicity, and safety of atezolizumab subcutaneous versus intravenous administration in previously treated locally advanced or metastatic non-small-cell lung cancer and pharmacokinetics comparison with other approved indications’: [Annals of Oncology 34 (2023) p693-702, (S0923753423006944), (10.1016/j.annonc.2023.05.009)]

M. Burotto*, Z. Zvirbule, A. Mochalova, Y. Runglodvatana, L. Herraez-Baranda, S. N. Liu, P. Chan, E. Shearer-Kang, X. Liu, N. Tosti, J. A. Zanghi, B. Leutgeb, E. Felip

*Autor correspondiente de este trabajo

Producción científica: Contribución a una revistaComentario/Debate

Resumen

The authors regret that there was an error to the Results section, page 697, of the published manuscript. The corrected sentence is shown below: Serious AEs occurred in 15.4% (n ¼ 38) of patients receiving atezolizumab SC and 17.7% (n ¼ 22) of patients receiving atezolizumab IV (Table 2). The authors would like to apologise for any inconvenience caused.

Idioma originalInglés
PublicaciónAnnals of Oncology
DOI
EstadoAceptada/en prensa - 2024
Publicado de forma externa

Nota bibliográfica

Publisher Copyright:
© 2023 European Society for Medical Oncology

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Profundice en los temas de investigación de 'Corrigendum to ‘IMscin001 Part 2: a randomised phase III, open-label, multicentre study examining the pharmacokinetics, efficacy, immunogenicity, and safety of atezolizumab subcutaneous versus intravenous administration in previously treated locally advanced or metastatic non-small-cell lung cancer and pharmacokinetics comparison with other approved indications’: [Annals of Oncology 34 (2023) p693-702, (S0923753423006944), (10.1016/j.annonc.2023.05.009)]'. En conjunto forman una huella única.

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