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High-Dose Methotrexate as CNS Prophylaxis in High-Risk Aggressive B-Cell Lymphoma

医学 内科学 甲氨蝶呤 侵袭性淋巴瘤 肿瘤科 淋巴瘤 美罗华 重症监护医学
作者
Katharine L. Lewis,Lasse Hjort Jakobsen,Diego Villa,Karin E. Smedby,Kerry J. Savage,Toby A. Eyre,Kate Cwynarski,Mark Bishton,Christopher P. Fox,Eliza A. Hawkes,Matthew J. Maurer,Tarec Christoffer El‐Galaly,Chan Y. Cheah,on behalf of the International CNS Prophylaxis Study Group,Sabela Bobillo,Paris L. Caporn,Joan Van Zyl,Magdalena Klánová,Marek Trněný,Robert Puckrin
出处
期刊:Journal of Clinical Oncology [Lippincott Williams & Wilkins]
卷期号:41 (35): 5376-5387 被引量:45
标识
DOI:10.1200/jco.23.00365
摘要

PURPOSE: CNS progression or relapse is an uncommon but devastating complication of aggressive B-cell lymphoma. There is no consensus regarding the optimal approach to CNS prophylaxis. This study was designed to determine whether high-dose methotrexate (HD-MTX) is effective at preventing CNS progression in patients at high risk of this complication. PATIENTS AND METHODS: Patients age 18-80 years with aggressive B-cell lymphoma and high risk of CNS progression, treated with curative-intent anti-CD20-based chemoimmunotherapy, were included in this international, retrospective, observational study. Cause-specific hazard ratios (HRs) and cumulative risks of CNS progression were calculated according to use of HD-MTX, with time to CNS progression calculated from diagnosis for all patients (all-pts) and from completion of frontline systemic lymphoma induction therapy, for patients in complete response at completion of chemoimmunotherapy (CR-pts). RESULTS: = .29), with 5-year adjusted risk difference of 1.6% (95% CI, -1.5 to 4.4; all-pts) and 1.4% (95% CI, -1.5 to 4.1; CR-pts). Subgroups were underpowered to draw definitive conclusions regarding the efficacy of HD-MTX in individual high-risk clinical scenarios; however, there was no clear reduction in CNS progression risk with HD-MTX in any high-risk subgroup. CONCLUSION: In this large study, high-risk patients receiving HD-MTX had a 7.2% 2-year risk of CNS progression, consistent with the progression risk in previously reported high-risk cohorts. Use of HD-MTX was not associated with a clinically meaningful reduction in risk of CNS progression.
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