Subcutaneous Rituximab-MiniCHOP Compared With Subcutaneous Rituximab-MiniCHOP Plus Lenalidomide in Diffuse Large B-Cell Lymphoma for Patients Age 80 Years or Older

医学 美罗华 来那度胺 长春新碱 弥漫性大B细胞淋巴瘤 内科学 强的松 环磷酰胺 切碎 胃肠病学 临床终点 淋巴瘤 外科 化疗 肿瘤科 随机对照试验 多发性骨髓瘤
作者
Lucie Obéric,Frédéric Peyrade,Mathieu Puyade,Christophe Bonnet,Peggy Dartigues-Cuillères,Bettina Fabiani,Philippe Ruminy,Hervé Maisonneuve,Julie Abraham,Catherine Thiéblemont,Pierre Soubeyran,Gilles Salles,Fontanet Bijou,Gianmatteo Pica,Gandhi Damaj,Corinne Haïoun,Olivier Casasnovas,H. Farhat,Ronan Le Calloch,Agathe Waultier‐Rascalou,Sandra Malak,Jérôme Paget,Elodie Gat,Hervè Tilly,Fabrice Jardin
出处
期刊:Journal of Clinical Oncology [Lippincott Williams & Wilkins]
卷期号:39 (11): 1203-1213 被引量:48
标识
DOI:10.1200/jco.20.02666
摘要

PURPOSE: The prognosis of elderly patients with diffuse large B-cell lymphoma (DLBCL) is worse than that of young patients. An attenuated dose of chemotherapy—cyclophosphamide, doxorubicin, vincristine, and prednisone plus rituximab (R-miniCHOP)—is a good compromise between efficacy and safety in very elderly patients. In combination with R-CHOP (R2-CHOP), lenalidomide has an acceptable level of toxicity and may mitigate the negative prognosis of the non–germinal center B-cell–like phenotype. The Lymphoma Study association conducted a multicentric, phase III, open-label, randomized trial to compare R-miniCHOP and R2-miniCHOP. PATIENTS AND METHODS: Patients of age 80 years or older with untreated DLBCL were randomly assigned into the R-miniCHOP21 group or the R2-miniCHOP21 group for six cycles and stratified according to CD10 expression and age. The first cycle of rituximab was delivered by IV on D1 after a prephase and then delivered subcutaneously on D1 of cycles 2-6. Lenalidomide was delivered at a dose of 10 mg once daily on D1-D14 of each cycle. The primary end point was overall survival (OS). RESULTS: A total of 249 patients with new DLBCL were randomly assigned (127 R-miniCHOP and 122 R2-miniCHOP). The median age was 83 years (range, 80-96), and 55% of the patients were classified as non-GCB. The delivered dose for each R-miniCHOP compound was similar in both arms. Over a median follow-up of 25.1 months, the intention-to-treat analysis revealed that R2-miniCHOP did not improve OS (2-year OS 66% in R-miniCHOP and 65.7% in R2-miniCHOP arm, P = .98) in the overall population or in the non-GCB population. Grade 3-4 adverse events occurred in 53% of patients with R-miniCHOP and in 81% of patients with R2-miniCHOP. CONCLUSION: The addition of lenalidomide to R-miniCHOP does not improve OS. Rituximab delivered subcutaneously was safe in this population.
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