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FDA Approves Rituximab Plus Chemotherapy for Paediatric Cancer Indications

Efficacy was evaluated in Inter-B-NHL Ritux 2010 global randomised study
10 Dec 2021
Anticancer agents & Biologic therapy;  Cancer in Special Situations / Population;  Haematologic malignancies

On 2 December 2021, the US Food and Drug Administration (FDA) approved rituximab (Rituxan, Genentech, Inc.) in combination with chemotherapy for paediatric patients (≥6 months to <18 years) with previously untreated, advanced stage, CD20-positive diffuse large B-cell lymphoma (DLBCL), Burkitt lymphoma (BL), Burkitt-like lymphoma (BLL), or mature B-cell acute leukaemia (B-AL).

Efficacy was evaluated in Inter-B-NHL Ritux 2010 (NCT01516580), a global multicentre, open-label, randomised (1:1) study of patients ≥6 months in age with previously untreated, advanced stage, CD20-positive DLBCL/BL/BLL/B-AL. Advanced stage was defined as Stage III with elevated lactose dehydrogenase (LDH) level (LDH greater than twice the institutional upper limit of normal values) or stage IV B-cell NHL or B-AL. Patients were randomised to Lymphome Malin B (LMB) chemotherapy (corticosteroids, vincristine, cyclophosphamide, high-dose methotrexate, cytarabine, doxorubicin, etoposide, and triple drug [methotrexate/cytarabine/corticosteroid] intrathecal therapy) alone or in combination with rituximab or non-US licensed rituximab, administered as 6 infusions of rituximab i.v. at a dose of 375 mg/m2 (2 doses during each of the 2 induction courses and 1 during each of the 2 consolidation courses) as per the LMB scheme. 

The main efficacy outcome measure was event-free survival (EFS), defined as progressive disease, relapse, second malignancy, death from any cause, or non-response as evidenced by detection of viable cells in residue after the second CYVE (Cytarabine [Aracytine, Ara-C], Veposide [VP16]) course, whichever occurs first. A prespecified interim efficacy analysis at 53% information fraction was performed in 328 randomised patients with a median follow-up of 3.1 years. There were 28 EFS events in the LMB group and 10 in the rituximab-LMB group (hazard ratio [HR] 0.32; 90% confidence interval [CI] 0.17, 0.58; p = 0.0012). At the time of the interim analysis, there were 20 deaths in the LMB chemotherapy arm compared to 8 deaths in the rituximab plus LMB chemotherapy arm, with an estimated overall survival (OS) HR of 0.36 (95% CI 0.16, 0.81). No formal statistical test was conducted for OS and the OS result is considered descriptive. Randomisation was discontinued after the interim analysis and an additional 122 patients received rituximab plus LMB chemotherapy and contributed to the safety analysis.

Adverse reactions (grade 3 or higher, >15%) occurring in paediatric patients treated with rituximab and chemotherapy were febrile neutropenia, stomatitis, enteritis, sepsis, increased alanine aminotransferase, and hypokalaemia. Grade 3 or higher adverse reactions that occurred more often in the rituximab plus LMB chemotherapy arm compared to LMB chemotherapy included sepsis, stomatitis, and enteritis. Fatal adverse reactions occurred in <2% of patients in both the rituximab plus LMB chemotherapy and LMB chemotherapy arms.

The recommended rituximab dose is 375 mg/m2 as an intravenous infusion given in combination with systemic LMB chemotherapy. In total, 6 infusions of rituximab are given, 2 doses during each of the induction courses, COPDAM1 [cyclophosphamide, Oncovin (vincristine), prednisolone, Adriamycin (doxorubicin), methotrexate] and COPDAM2, and 1 dose during each of the 2 consolidation courses of CYM (Cytarabine [Aracytine, Ara-C], methotrexate) and CYVE.

Full prescribing information for Rituxan is available here.

This review used the Assessment Aid, a voluntary submission from the applicant to facilitate the FDA’s assessment, and Streamlined Review.

This application was granted priority review.

Healthcare professionals should report all serious adverse events suspected to be associated with the use of any medicine and device to FDA’s MedWatch Reporting System.

For assistance with single-patient INDs for investigational oncology products, healthcare professionals may contact FDA’s Oncology Center of Excellence Project Facilitate.

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