首页> 外文期刊>Journal of neuro-oncology. >Early relapses in patients with primary CNS lymphoma treated with methotrexate-based chemotherapy without consolidating whole brain irradiation.
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Early relapses in patients with primary CNS lymphoma treated with methotrexate-based chemotherapy without consolidating whole brain irradiation.

机译:原发性中枢神经系统淋巴瘤患者以甲氨蝶呤为基础的化学疗法治疗后,其早期复发并未巩固全脑照射。

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摘要

Methotrexate (MTX)-based chemotherapy is used as upfront treatment for most patients with primary CNS lymphoma. Whether consolidating whole brain irradiation (WBI) should be recommended for patients who achieve complete remission (CR) is still a matter of debate. Patients who are predicted to experience an early relapse (ER, ≤12 months from diagnosis) might especially benefit from consolidating treatment. We therefore evaluated the incidence and prognostic impact of ER in patients with CR following chemotherapy without WBI. We identified 40 patients between 2000 and 2010 who had achieved CR following MTX-based chemotherapy. Of 36 evaluable patients 11 (31 %) experienced an ER. These patients had significantly impaired overall survival (46.0 vs. 79.0 months, p = 0.001). Normal cerebrospinal fluid cell count (11.0 vs. 76.0 months, p = 0.001) and frequent reduction of MTX dose due to impaired creatinine clearance (10.0 vs. 48.0 months, p = 0.005) had a significantly negative impact on relapse-free survival. Patients with CR following MTX-based induction chemotherapy represent a heterogeneous population. In these patients, ER is an independent risk factor for impaired overall survival. Therefore, these patients might especially benefit from consolidating treatment. These results have to be validated by prospective trials.
机译:对于大多数原发性CNS淋巴瘤患者,基于甲氨蝶呤(MTX)的化疗被用作前期治疗。是否应该为达到完全缓解(CR)的患者推荐巩固全脑照射(WBI)仍是一个有争议的问题。预计将经历早期复发(ER,诊断后≤12个月)的患者可能特别受益于巩固治疗。因此,我们评估了无WBI化疗后CR患者CR的发生率和预后影响。我们确定了2000年至2010年之间40位在基于MTX的化疗后获得CR的患者。在36名可评估患者中,有11名(31%)经历了ER。这些患者的总生存期显着受损(46.0 vs. 79.0个月,p = 0.001)。正常的脑脊髓液细胞计数(11.0 vs. 76.0个月,p = 0.001)以及由于肌酐清除率受损而频繁减少MTX剂量(10.0 vs. 48.0个月,p = 0.005)对无复发生存具有显着的负面影响。基于MTX的诱导化疗后的CR患者代表异质性人群。在这些患者中,ER是影响整体生存的独立危险因素。因此,这些患者可能特别受益于巩固治疗。这些结果必须通过前瞻性试验进行验证。

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