Subgroup analysis of older patients ≥60 years with diffuse large B-cell lymphoma in the phase 3 POLARIX study
In the phase 3 POLARIX study, Pola-R-CHP (polatuzumab vedotin plus rituximab, cyclophosphamide, doxorubicin, and prednisone) improved progression-free survival (PFS) vs R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) in patients with previously untreated diffuse large B-cell lymphoma (DLBCL). This post hoc subgroup analysis of POLARIX evaluated the efficacy and safety of Pola-R-CHP vs R-CHOP in older patients aged ≥60, ≥65, ≥70, and ≥75 years. As of 15 June 2022 (median follow-up, 40 months), 629 patients aged ≥60 years were included (Pola-R-CHP, n = 311; R-CHOP, n = 318). Clinically meaningful improvements in PFS with Pola-R-CHP vs R-CHOP were observed across all age groups, particularly in patients aged ≥70 years whereby the risk of disease progression, relapse, or death was reduced by 37% (unstratified hazard ratio [HR], 0.63; 95% confidence interval [CI], 0.41-0.96). In patients aged ≥60 years, overall survival was similar with Pola-R-CHP vs R-CHOP (unstratified HR, 0. 99; 95% CI, 0.67-1.47). Safety profiles were similar for Pola-R-CHP vs R-CHOP among patients aged ≥60 years, including rates of grade 3 to 4 adverse events (AEs; 62.7% vs 61.5%), grade 3 to 5 infections (15.0% vs 12.9%), and grade 5 AEs (3.6% vs 3.2%); no novel toxicities were reported. Incidence of grade 3 to 4 febrile neutropenia was higher with Pola-R-CHP than R-CHOP (16.3% vs 7.6%), highlighting the importance of granulocyte colony-stimulating factor prophylaxis in older patients receiving Pola-R-CHP. The benefit-risk profile favored Pola-R-CHP vs R-CHOP in older patients with previously untreated DLBCL. This trial was registered at www.ClinicalTrials.gov as #NCT03274492.
Authors
- Austin I. Kim (ORCID: https://orcid.org/0000-0003-1039-0658)
- Matthew Sugidono (ORCID: https://orcid.org/0000-0003-4883-8921)
- Huilai Zhang (ORCID: https://orcid.org/0000-0002-8558-3131)
- H. Tilly
- Jeff Porter Sharman (ORCID: https://orcid.org/0000-0001-5611-6115)
- Laurie H. Sehn (ORCID: https://orcid.org/0000-0003-1860-9765)
- Bei Hu (ORCID: https://orcid.org/0000-0002-4325-0929)
- Dai Maruyama (ORCID: https://orcid.org/0000-0003-0654-6920)
- Charles Herbaux (ORCID: https://orcid.org/0000-0003-4910-476X)
- Connie Lee Batlevi (ORCID: https://orcid.org/0000-0002-9036-9463)
- Rucha Kothari
- Jamie Hirata
- Mark Hertzberg (ORCID: https://orcid.org/0000-0001-8495-4669)
- Patrick M. Reagan (ORCID: https://orcid.org/0000-0002-7155-7063)
- Saibah Chohan
- Deniz Şahin (ORCID: https://orcid.org/0000-0002-3189-6810)
- Frank Stenner (ORCID: https://orcid.org/0000-0003-4541-8817)
- Calvin Lee (ORCID: https://orcid.org/0000-0003-0716-8925)
- Lysiane Molina
Institutions
- Roche (Switzerland) (CH)
- BC Cancer Agency (CA)
- Centre Hospitalier Universitaire de Grenoble (FR)
- Spinal Cord Injury BC (CA)
- University Hospital of Basel (CH)
- Tianjin Medical University Cancer Institute and Hospital (CN)
- University of Rochester Medical Center (US)
- Roche (Canada) (CA)
- Centre Hospitalier Universitaire de Montpellier (FR)
- Levine Cancer Institute (US)
- Prince of Wales Hospital (AU)
- Dana-Farber Cancer Institute (US)
- Laboratoire National Henri Becquerel (FR)
- Willamette Valley Cancer Institute and Research Center (US)
- Japanese Foundation For Cancer Research (JP)
- Centre Henri Becquerel (FR)
- University of Rochester (US)
- Université de Rouen Normandie (FR)
- Université Grenoble Alpes (FR)
Publication Details
- Journal
- Blood Advances
- Published
- 2025-03-14
- DOI
- https://doi.org/10.1182/bloodadvances.2024014707
- Citations
- 7
- Primary Topic
- Lymphoma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 10.30