Home > Haematology > ASH 2021 > Lymphoma > POLARIX: Novel regimen superior to R-CHOP in DLBCL

POLARIX: Novel regimen superior to R-CHOP in DLBCL

Presented by
Prof. Hervé Tilly, University of Rouen, France
Conference
ASH 2021
Trial
Phase 3, POLARIX
Polatuzumab vedotin added to rituximab, cyclophosphamide, doxorubicin, and prednisone (Pola-R-CHP) outperformed the standard-of-care regimen of rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) as initial treatment in patients with diffuse large B-cell lymphoma (DLBCL). The safety profiles of the 2 regimens were comparable [1].

Prof. Hervé Tilly (University of Rouen, France) explained that R-CHOP, the standard-of-care regimen for patients with DLBCL, is effective in 60–70% of patients with this condition. In the last 20 years, adaptations to the R-CHOP treatment regimen have not succeeded in meeting the unmet need in this population.

The current, randomised, double-blind, phase 3 POLARIX trial (NCT03274492) added polatuzumab vedotin, an antibody drug conjugate targeting CD79b, to rituximab, cyclophosphamide, doxorubicin, and prednisone. Patients with previously untreated DLBCL (n=879) were randomised 1:1 to 6 cycles of Pola-R-CHP (with 1.8 mg/kg IV polatuzumab vedotin on day 1 of a 21-day cycle) or R-CHOP. The primary endpoint was progression-free survival.

After a median follow-up of 28 months, the Pola-R-CHP regimen showed superiority over the R-CHOP regimen regarding progression-free survival (HR 0.73; P<0.02). Similarly, patients in the Pola-R-CHP arm displayed higher event-free survival rates than patients in the R-CHOP arm (HR 0.75; P=0.02). Although overall response rates did not significantly differ between treatment groups, disease-free survival rates (HR 0.70) indicated that patients who achieved a complete response in the Pola-R-CHP arm were more likely to maintain remission than patients in the R-CHOP arm who reached a complete response. The overall survival rates were 88.6% in both groups. Notably, patients treated with Pola-R-CHP received fewer subsequent therapies (22.5%) than patients treated with R-CHOP (30.3%). Exploratory subgroup analyses are ongoing to further specify the results of the POLARIX trial.

The safety profiles of the 2 regimens were comparable, with approximately 57% of the patients in both treatment groups experiencing grade 3 or 4 adverse events (AEs). Although febrile neutropenia and diarrhoea were more common in the Pola-R-CHP condition, treatment with Pola-R-CHP led to fewer dose reductions (9.2%) than treatment with R-CHOP (13.2%). The prevalence of peripheral neuropathy was similar in both research arms.

  1. Tilly H, et al. The POLARIX Study: Polatuzumab Vedotin with Rituximab, Cyclophosphamide, Doxorubicin, and Prednisone (pola-R-CHP) Versus Rituximab, Cyclophosphamide, Doxorubicin, Vincristine and Prednisone (R-CHOP) Therapy in Patients with Previously Untreated Diffuse Large B-Cell Lymphoma. LBA-1, ASH 2021 Annual Meeting, 11–14 December.

 

Copyright ©2022 Medicom Medical Publishers



Posted on