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Outcomes of Rituximab-abbs versus Rituximab in Patients with Diffuse Large B-Cell Lymphoma in a Noninferiority Study.
Wong, Helen W; Nguyen, Vivian H; Mok, Timothy Y; Niu, Fang; Cushing, Merta; Lam, Michael; Ho, Stephanie L; Law, Lisa; Aziz, Ashraf R; Hui, Rita L.
Afiliação
  • Wong HW; Kaiser Permanente Oakland, Oakland, CA, USA.
  • Nguyen VH; Kaiser Permanente San Diego, San Diego, CA, USA.
  • Mok TY; Kaiser Permanente Drug Use Management-Clinic Administered and Specialty Medications, Oakland, CA, USA.
  • Niu F; Kaiser Permanente Pharmacy Outcomes Research Group, Downey, CA, USA.
  • Cushing M; Kaiser Permanente San Diego, San Diego, CA, USA.
  • Lam M; Kaiser Permanente South San Francisco, South San Francisco, CA, USA.
  • Ho SL; Kaiser Permanente Drug Intelligence and Strategy, Oakland, CA, USA.
  • Law L; Kaiser Permanente Roseville, Roseville, CA, USA.
  • Aziz AR; Kaiser Permanente Irvine, Irvine, CA, USA.
  • Hui RL; Kaiser Permanente Pharmacy Outcomes Research Group, 1800 Harrison St, Oakland, CA, 94612, USA. Rita.L.Hui@kp.org.
BioDrugs ; 38(4): 601-610, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38935234
ABSTRACT

BACKGROUND:

Rituximab with cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) is one of the first line treatments for diffuse large B-cell lymphoma (DLBCL). Rituximab comprises most of the treatment cost for this regimen; therefore, biosimilars, such as rituximab-abbs are crucial to provide affordable care. Although rituximab-abbs was studied primarily in follicular lymphoma, the Food and Drug Administration (FDA) approved this drug for all indications of the reference product on the basis of extrapolation. Effectiveness and safety data surrounding the use of rituximab-abbs in DLBCL is lacking.

OBJECTIVE:

To evaluate the effectiveness and safety of rituximab-abbs and reference product rituximab as R-CHOP treatment for patients with DLBCL. PATIENTS AND

METHODS:

This noninferiority (NI) study compared the 2-year overall survival (OS), overall response rate (ORR), and incidence of adverse events (AEs) between rituximab-abbs and its reference product (RP) in R-CHOP among adult patients with newly diagnosed DLBCL. The study inclusion period was from 1 January 2019 to 31 December 2020. Analyses were performed on the basis of a noninferiority lower limit of 10% for OS and ORR, and an upper limit of 10% for serious AEs.

RESULTS:

There were 240 patients who received RP rituximab, while 295 patients received rituximab-abbs. The cohort had a mean age of 63.7±12.2 years and 43% were female. The 2-year OS was 81.0% and 79.6% (NI p < 0.01) while the ORR was 80.0% and 69.6% (NI p < 0.01), among the rituximab-abbs and rituximab groups, respectively. The incidence of infusion reaction AEs (NI p < 0.01) and noninfusion reaction AEs (NI p < 0.01) also met noninferiority.

CONCLUSIONS:

We demonstrated that rituximab-abbs was noninferior to rituximab in both effectiveness and safety among patients receiving R-CHOP for DLBCL in this study. Long-term follow-up would be needed to confirm these results.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vincristina / Prednisona / Protocolos de Quimioterapia Combinada Antineoplásica / Doxorrubicina / Linfoma Difuso de Grandes Células B / Ciclofosfamida / Rituximab Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: BioDrugs Assunto da revista: ALERGIA E IMUNOLOGIA / GENETICA MEDICA / TERAPEUTICA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Nova Zelândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vincristina / Prednisona / Protocolos de Quimioterapia Combinada Antineoplásica / Doxorrubicina / Linfoma Difuso de Grandes Células B / Ciclofosfamida / Rituximab Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: BioDrugs Assunto da revista: ALERGIA E IMUNOLOGIA / GENETICA MEDICA / TERAPEUTICA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Nova Zelândia