Skip to main content

Advertisement

Advertisement

ADVERTISEMENT

Research in Review

Does Intensified Therapy Improve Prognosis in DLBCL?

Recent research compared the effects of standard chemotherapy dosage with intensified chemotherapy for patients with high-risk diffuse large B-cell lymphoma (DLBCL), published in The Lancet Oncology (published online June 28, 2017; doi:10.1016/S1470-2045(17)30444-8).

Prognoses of younger patients with high-risk DLBCL (age adjusted International Prognostic Index score, 2-3) treated with rituximab, cyclophosphamide, vincristine, doxorubicin, and prednisone (R-CHOP) are poor. Limited research exists regarding the variation of standard R-CHOP dosing to treat younger patients with such disease.

Annalisa Chiappella, MD, department of hematology, Azienda Ospedaliero Universitaria Città della Salute e della Scienza di Torino (Italy), and colleagues conducted a study to investigate a potential benefit of intensification with high-dose chemotherapy and autologous stem-cell transplantation (ASCT) as a substitute for first-line treatment of younger patients with DLBCL. A total of 399 patients were randomly assigned to receive either of two different R-CHOP dose levels – a full course of rituximab-dose-dense chemotherapy (no transplantation group) or an abbreviated course of rituximab-dose-dense chemotherapy followed by consolidation with rituximab plus high-dose cytarabine plus mitoxantrone (R-MAD) plus dexamethasone and high-dose BEAM chemotherapy (carmustine, etoposide, cytarabine, and melphalan) plus ASCT (transplantation group).

After a median follow-up of 72 months, 2-year failure-free survival was 71% in the transplantation group compared with 62% in the no transplantation group. No significant difference in 5-year overall survival was recorded between these groups (78% vs 77%, respectively).

Grade 3 or worse hematological adverse events were reported in 92% of patients in the transplantation group and 68% of patients in the no transplantation group. Grade 3 or worse non-hematological adverse events were reported in 45% versus 16%, respectively.

While researchers concluded that abbreviated rituximab-dose-dense chemotherapy plus R-MAD plus BEAM and ASCT reduced the risk of treatment failure compared with full course rituximab-dose-dense chemotherapy in younger patients with high-risk DLBCL, the results were not clinically meaningful due to the lack of improvement in overall survival. “These results do not support further consideration of the use of intensification of R-CHOP as an upfront strategy in patients with DLBCL with poor prognosis,” they wrote.—Zachary Bessette

Advertisement

Advertisement

Advertisement