Rituximab biosimilar RTXM83 versus reference rituximab in combination with CHOP as first-line treatment for diffuse large B-cell lymphoma: a randomized, double-blind study


Candelaria M., Gonzalez D. E., Delamain M. T., Bar D. O., Beniwal S. K., Dasappa L., ...Daha Fazla

LEUKEMIA & LYMPHOMA, cilt.60, sa.14, ss.3375-3385, 2019 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 60 Sayı: 14
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1080/10428194.2019.1633632
  • Dergi Adı: LEUKEMIA & LYMPHOMA
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.3375-3385
  • Anahtar Kelimeler: Rituximab, RTXM83, biosimilar drug, diffuse large B-cell lymphoma, clinical trial, CHEMOTHERAPY PLUS RITUXIMAB, FEBRILE NEUTROPENIA, YOUNG-PATIENTS, PHARMACOKINETICS, GUIDELINES, CANCER, TRIAL, RISK
  • Dokuz Eylül Üniversitesi Adresli: Evet

Özet

This multicenter, double-blind, randomized study compared the efficacy, pharmacokinetics (PKs)/pharmacodynamics (PDs), safety and immunogenicity profile of RTXM83 vs. reference rituximab (R-rituximab), both with CHOP, as first-line treatment of diffuse large B-cell lymphoma (DLBCL). A total of 272 patients <65 years of age, with good prognosis (136 per arm) were randomized (1:1) to receive six cycles of either RTXM83 or R-rituximab. The primary efficacy endpoint was achieved (overall response rate of 83.6% for RTXM83 and 82.9% for R-rituximab) with a difference 0.7% between arms (95%CI: [-8.77% to 10.17%]) fulfilling the predefined non-inferiority margin (-13%). Similar number of patients reported at least one adverse event (AE) (131 per arm) or one serious AE (47 with RTXM83 and 45 with R-rituximab). Anti-drug antibody development was comparable between the arms. PK/PD secondary endpoint results support similarity between the compounds. RTXM83 exhibits non-inferior efficacy and similar safety/immunogenicity to R-rituximab, being an accessible alternative for the treatment of patients with previously untreated DLBCL.