Obinutuzumab vs rituximab for transplant-eligible patients with mantle cell lymphoma

医学 内科学 美罗华 套细胞淋巴瘤 奥比努图库单抗 肿瘤科 伊布替尼 淋巴瘤 慢性淋巴细胞白血病 白血病
作者
Clémentine Sarkozy,Mary Callanan,Catherine Thiéblemont,Lucie Obéric,Barbara Burroni,Krimo Bouabdallah,Gandhi Damaj,Benoît Tessoulin,Vincent Ribrag,Roch Huout,Franck Morschhauser,Samuel Griolet,Clémentine Joubert,Victoria Cacheux,Vincent Delwail,Violaine Safar,Rémy Gressin,Morgane Cheminant,Marie‐Hélène Delfau‐Larue,Olivier Hermine
出处
期刊:Blood [American Society of Hematology]
卷期号:144 (3): 262-271 被引量:9
标识
DOI:10.1182/blood.2024023944
摘要

Abstract Obinutuzumab (O) and rituximab (R) are 2 CD antibodies that have never been compared in a prospective randomized trial of mantle cell lymphoma (MCL). Herein, we report the long-term outcome of the LyMa-101 trial, in which newly diagnosed patients with MCL were treated with chemotherapy plus O before transplantation, followed by O maintenance (O group). We then compared these patients with those treated with the same treatment design with R instead of O (R group). A propensity score matching (PSM) was used to compare the 2 populations (O vs R groups) in terms of measurable residual disease (MRD) at the end of induction (EOI), progression-free survival (PFS), and overall survival (OS). In LyMa-101, the estimated 5-year PFS and OS after inclusion (n = 85) were 83.4% (95% confidence interval [CI], 73.5-89.8) and 86.9% (95% CI, 77.6-92.5), respectively. At EOI, patients treated in the O group had more frequent bone marrow MRD negativity than those treated in the R group (83.1% vs 63.4%; χ2, P = .007). PSM resulted in 2 sets of 82 patients with comparable characteristics at inclusion. From treatment initiation, the O group had a longer estimated 5-year PFS (P = .029; 82.8% vs 66.6%; hazard ratio [HR], 1.99; 95% confidence interval (CI), 1.05-3.76) and OS (P = .039; 86.4% vs 71.4%; HR, 2.08; 95% CI, 1.01-4.16) compared with the R group. Causes of death were comparable in the 2 groups, the most common cause being lymphoma. O before transplantation and in maintenance provides better disease control and enhances PFS and OS compared with R in transplant-eligible patients with MCL. These trials were registered at www.clinicaltrials.gov as #NCT00921414 and NCT02896582.
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