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Real-world progression-free survival in first-line advanced non-small cell lung cancer treated with immunotherapy-based regimens using a US dataset.
Waterhouse, David; Lam, Jenny; Betts, Keith A; Yin, Lei; Gao, Sophie; Yuan, Yong; Hartman, John; Rao, Sumati; Lubinga, Solomon; Stenehjem, David.
  • Waterhouse D; OHC Cincinnati, Cincinnati, OH, USA.
  • Lam J; Bristol Myers Squibb, Lawrenceville, NJ, USA.
  • Betts KA; Analysis Group, Los Angeles, CA, USA.
  • Yin L; Analysis Group, Los Angeles, CA, USA.
  • Gao S; Analysis Group, Los Angeles, CA, USA.
  • Yuan Y; Bristol Myers Squibb, Lawrenceville, NJ, USA.
  • Hartman J; Bristol Myers Squibb, Lawrenceville, NJ, USA.
  • Rao S; Bristol Myers Squibb, Lawrenceville, NJ, USA.
  • Lubinga S; Bristol Myers Squibb, Lawrenceville, NJ, USA.
  • Stenehjem D; University of Minnesota, Minneapolis, MN, USA.
Data Brief ; 37: 107195, 2021 Aug.
Article en En | MEDLINE | ID: mdl-34169127
While results from clinical trials are important in determining the efficacy of treatment, restrictive eligibility criteria may limit generalizability to patient populations in the real-world setting. Real-world analyses can therefore identify subgroups of patients who may respond differently to specific therapeutic regimens. This supplementary data is supportive to the research article entitled "Real-world outcomes of immunotherapy-based regimens in first-line advanced non-small cell lung cancer" [1]. Using electronic health records data from a large demographically and geographically diverse oncology database, we present real-world progression-free survival (rwPFS) outcomes for patients with advanced non-small cell lung cancer in the United States treated with either first-line immunotherapy as monotherapy or single-agent immunotherapy combined with chemotherapy. rwPFS was estimated for patients in each treatment group using Kaplan-Meier methods; analyses were conducted separately for patients with squamous and non-squamous histology and stratified by Eastern Cooperative Oncology Group performance status, tumor programmed death ligand-1 expression, and presence of brain metastases.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Article