In a European Intergroup for Childhood Non-Hodgkin Lymphoma/Children’s Oncology Group phase III trial reported in The New England Journal of Medicine, Minard‑Colin et al found that the addition of rituximab to standard Lymphomes Malin B (also known as Lymphome Malin de Burkitt, or LMB) chemotherapy significantly improved event-free and overall survival in children with high-risk, mature B-cell non-Hodgkin lymphoma. Rituximab/chemotherapy was also associated with numerically higher rates of severe febrile neutropenia and infection and a significantly higher rate of low immunoglobulin G levels.
As stated by the investigators, “Rituximab added to chemotherapy prolongs survival among adults with B-cell cancer. Data on its efficacy and safety in children with high-grade, mature B-cell non-Hodgkin’s lymphoma are limited.”
The open-label trial included 328 patients (main analysis population) from 12 countries aged 6 months to 18 years with newly diagnosed, high-risk, mature B-cell non-Hodgkin lymphoma (stage III with elevated lactate dehydrogenase [LDH] or stage IV) or acute leukemia. Patients were randomly assigned between December 2011 and November 2015 to receive rituximab plus standard LMB chemotherapy (n = 164) or LMB chemotherapy alone (n = 164).
Rituximab was given at 375 mg/m2 on 2 days before and day 1 of the two induction chemotherapy courses and on day 1 of the two consolidation courses (six total doses). All patients received prephase treatment with low-dose cyclophosphamide, vincristine, and prednisone. The primary endpoint was event-free survival.
When comparing the rituximab/chemotherapy vs chemotherapy-alone groups:
Median follow-up was 39.9 months. Events occurred in 10 patients in the rituximab/chemotherapy group vs 28 in the chemotherapy group, with the greatest difference between groups being the occurrence of relapse or disease progression in 3 vs 23 patients. Event-free survival at 3 years was 93.9% (95% confidence interval [CI] = 89.1%–96.7%) in the rituximab/chemotherapy group vs 82.3% (95% CI = 75.7%–87.5%) in the chemotherapy group (hazard ratio [HR] = 0.32, P = .00096).
The event-free survival benefit of rituximab/chemotherapy was observed across subgroups of patients, including among group B patients (HR = 0.33, 95% CI = 0.12–0.91), group C1 patients (HR = 0.37, 95% CI = 0.12–1.18), and group C3 patients (HR = 0.19, 95% CI = 0.02–1.73) and among patients with Burkitt lymphoma (HR = 0.36, 95% CI = 0.16–0.77). By age group, hazard ratios were 0.26 (95% CI = 0.06–1.22) for age younger than 6 years, 0.13 (95% CI = 0.03–0.59) for 6 to less than 12 years, and 0.72 (95% CI = 0.24–2.14) for those aged 12 years or older.
Eight patients in the rituximab/chemotherapy group died, with four of those deaths being disease-related; three, treatment-related; and one, due to a second cancer. Death occurred in 20 patients in the chemotherapy group, with 17 being disease-related and 3, treatment-related. Overall survival at 3 years was 95.1% (95% CI = 90.5%–97.5%) vs 87.3% (95% CI = 81.2%–91.6%), with a hazard ratio of 0.36 (95% CI= 0.16–0.82).
After prephase treatment, grade ≥ 4 adverse events occurred in 33.3% of patients in the rituximab/chemotherapy group vs 24.2% of the chemotherapy group (P = .07). Grade ≥ 4 febrile neutropenia occurred in 11.7% vs 6.5% of patients (P = 0.11; grade 3 in 81% vs 84%) and grade ≥ 4 infection occurred in 18.5% vs 11.1% (P = .07; grade 3 in 40% vs 38%).
A greater proportion of patients in the rituximab/chemotherapy group had immunoglobulin G levels below the limit of normal range at end of therapy (70.3% vs 46.8%, P = .002) and at 1 year (55.9% vs 25.4%, P < .001). A greater proportion also received intravenous immune globulin (15.8% vs 7.0%), with the primary reason being low immunoglobulin level without infection; seven vs three patients continued to receive immune globulin at 1 year after enrollment.
As stated by the investigators, “Complete and longer follow-up with regard to immune status and late infections have not been evaluated.”
They concluded, “Rituximab added to standard LMB chemotherapy markedly prolonged event-free survival and overall survival among children and adolescents with high-grade, high-risk, mature B-cell non-Hodgkin lymphoma and was associated with a higher incidence of hypogammaglobulinemia and, potentially, more episodes of infection.”
Disclosure: The study was funded by the Clinical Research Hospital Program of the French Ministry of Health, Cancer Research UK, National Institute for Health Research Clinical Research Network, Children’s Cancer Foundation Hong Kong, National Cancer Institute, and F. Hoffmann–La Roche–Genentech. For full disclosures of the study authors, visit nejm.org.The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.