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Assessment of rituximab-abbs, a biosimilar, and rituximab outcomes in patients with CLL or NHL: A real-world UK study.
McBride, Ali; Daniel, Shoshana; Driessen, Maurice T; Szende, Agota; Choudhry, Azhar; Tian, Marc; Ariely, Rinat; Thompson, Stephen.
Afiliação
  • McBride A; Hematology/Oncology, Department of Pharmacy, The University of Arizona Cancer Center, 3838 N Campbell Ave, Tucson, AZ, 85749, USA. Electronic address: mcbride@pharmacy.arizona.edu.
  • Daniel S; Covance, 9801 Washingtonian Blvd, Gaithersburg, MD, 20878, USA. Electronic address: Shoshana.Daniel@Covance.com.
  • Driessen MT; Teva Pharmaceuticals Inc., Piet Heinkade 107, 1019 BRA, Amsterdam, the Netherlands. Electronic address: Maurice.Driessen@Tevaeu.com.
  • Szende A; Covance, Springfield House, Hyde St, Woodhouse, Leeds, LS2 9LH, UK. Electronic address: Agota.Szende@covance.com.
  • Choudhry A; Teva Pharmaceuticals Industries, Inc., 145 Brandywine Pkwy, West Chester, PA, 19380, USA. Electronic address: Azhar.Choudhry@tevapharm.com.
  • Tian M; Teva Pharmaceuticals Industries, Inc., 145 Brandywine Pkwy, West Chester, PA, 19380, USA. Electronic address: Marc.Tian@tevapharm.com.
  • Ariely R; Teva Pharmaceuticals Inc., 400 Interpace Pkwy #3, Parsippany, NJ, 07054, USA. Electronic address: Rinat.Ariely@tevapharm.com.
  • Thompson S; Teva Pharmaceuticals Inc., 400 Interpace Pkwy #3, Parsippany, NJ, 07054, USA. Electronic address: Stephen.Thompson01@tevapharm.com.
Leuk Res ; 111: 106671, 2021 12.
Article em En | MEDLINE | ID: mdl-34530254
BACKGROUND: Rituximab (chimeric anti-CD20 monoclonal antibody) treatment is approved for chronic lymphocytic leukemia (CLL) and non-Hodgkin lymphoma (NHL). Rituximab-abbs (first biosimilar approved in 2017) is expected to significantly reduce healthcare economic burden due to lower acquisition costs. This non-interventional, non-comparative study assessed real-world effectiveness and tolerability of rituximab-abbs and rituximab in treatment-naive patients with CLL or NHL. MATERIALS AND METHODS: Via an online physician survey, 46 UK-registered hematologists and oncologists retrospectively reported on randomly selected patients aged ≥18 years with CLL or NHL with rituximab-abbs or rituximab as first-line immunotherapy. Overall, 201 patient charts were examined across 4 cohorts: rituximab-abbs in CLL, rituximab-abbs in NHL, rituximab in CLL, rituximab in NHL. RESULTS: Demographic profiles across cohorts were similar. Most patients (94 %-100 %) received combination therapy (rituximab-abbs or rituximab mainly with chemotherapy). For both treatments, overall response rate (94 %-98 %) and 1-year overall survival (98 %-100 %) were very high for patients with CLL or NHL. Most common serious adverse events were neutropenia, fatigue, anemia and infusion reactions. The majority of patients (54 %-66 %) did not experience a grade ≥3 adverse event. Healthcare resource utilization was similarly high across cohorts, driven by diagnostic testing, oncologist office visits, and day-case hospital admissions; many patients required supportive medical therapies. Mean annual savings of ∼£1000/patient driven by acquisition costs occurred with rituximab-abbs versus rituximab, administration costs were similar. CONCLUSION: Rituximab-abbs and rituximab demonstrated similar effectiveness and tolerability in treating CLL and NHL in routine UK clinical practice and demonstrate the utility of the biosimilar as a cost-saving alternative treatment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article