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新诊断的原发性中枢神经系统淋巴瘤患者强化大剂量甲氨蝶呤方案治疗结局的改善:一项真实世界队列研究

Improvement of outcomes of an escalated high-dose methotrexate-based regimen for patients with newly diagnosed primary central nervous system lymphoma: a real-world cohort study.

作者信息

Li Qing, Ma Jingjing, Ma Yan, Lin Zhiguang, Kang Hui, Chen Bobin

机构信息

Department of Hematology, Huashan Hospital North, Fudan University, Shanghai, 201907, People's Republic of China.

Department of Hematology, Huashan Hospital, Fudan University, Shanghai, 200040, People's Republic of China.

出版信息

Cancer Manag Res. 2021 Aug 4;13:6115-6122. doi: 10.2147/CMAR.S322467. eCollection 2021.

Abstract

PURPOSE

High-dose methotrexate (HD-MTX)-based chemotherapy regimen is the first-line treatment of primary central nervous system lymphoma (PCNSL). At present, doses of MTX in the range of 3.5-8 g/m are frequently used. However, the optimal dose of methotrexate for PCNSL remains controversial. The purpose of this real-world study was to compare the efficacy and toxicity of HD-MTX in patients with untreated PCNSL.

METHODS

Immunocompetent adults with newly diagnosed PCNSL between January 2015 and December 2018 were investigated and followed up to June 2019. All patients' initial treatments were based on HD-MTX chemotherapy regimens.

RESULTS

A total of 73 patients were reviewed. For patients who received HD-MTX at 8 g/m vs.3.5 g/m, the complete response (CR) rates were 68.29% vs 43.75% (p = 0.03), and the median PFS times were 17.7 months vs 9.05 months (HR=0.455, 95% CI 0.239-0.865, p=0.016). There was no significant difference in OS between the two groups. Serious adverse effects were uncommon and clinically manageable.

CONCLUSION

There is a correlation of treatment response and clinical outcomes between the dosage of MTX in initial induction therapy in newly diagnosed PCNSL. MTX dose of 8 g/m provided a higher CR rate and PFS benefits with acceptable adverse effects.

摘要

目的

基于大剂量甲氨蝶呤(HD-MTX)的化疗方案是原发性中枢神经系统淋巴瘤(PCNSL)的一线治疗方法。目前,常用的甲氨蝶呤剂量范围为3.5-8g/m²。然而,PCNSL的最佳甲氨蝶呤剂量仍存在争议。本真实世界研究的目的是比较HD-MTX在未经治疗的PCNSL患者中的疗效和毒性。

方法

对2015年1月至2018年12月期间新诊断为PCNSL的免疫功能正常的成年人进行调查,并随访至2019年6月。所有患者的初始治疗均基于HD-MTX化疗方案。

结果

共纳入73例患者。接受8g/m² HD-MTX治疗的患者与接受3.5g/m² HD-MTX治疗的患者相比,完全缓解(CR)率分别为68.29%和43.75%(p=0.03),中位无进展生存期分别为17.7个月和9.05个月(HR=0.455,95%CI 0.239-0.865,p=0.016)。两组总生存期无显著差异。严重不良反应不常见且临床可管理。

结论

新诊断的PCNSL初始诱导治疗中甲氨蝶呤的剂量与治疗反应和临床结果之间存在相关性。8g/m²的甲氨蝶呤剂量可提供更高的CR率和无进展生存期益处,且不良反应可接受。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6331/8349527/8cce29576d79/CMAR-13-6115-g0001.jpg

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