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FAB/LMB 96 方案治疗期间或治疗后发生难治或复发的成熟 B 细胞非霍奇金淋巴瘤患儿和青少年的总生存:来自 FAB/LMB 96 研究组的报告。

Overall survival of children and adolescents with mature B cell non-Hodgkin lymphoma who had refractory or relapsed disease during or after treatment with FAB/LMB 96: A report from the FAB/LMB 96 study group.

机构信息

Maria Fareri Children's Hospital, New York Medical College, Valhalla, NY, USA.

Gustave Roussy, Villejuif, France.

出版信息

Br J Haematol. 2018 Sep;182(6):859-869. doi: 10.1111/bjh.15491. Epub 2018 Jul 9.

Abstract

We determined the risk factors associated with poor survival in children and adolescents with de novo mature B cell non-Hodgkin lymphoma (B-NHL) who had refractory or relapsed disease during or after the French-American-British mature lymphoma B (FAB/LMB) 96 multi-agent chemotherapy. Among the 1 111 registered on study, 104 patients (9·4%) had refractory disease or disease relapse after first complete remission. Among these 104 patients, 28 (27%) patients had refractory disease and 76 (73%) had relapsed disease. The estimated 1- and 2-year overall survival (OS) (95% confidence interval) was 31·5% (23·3-41·0%) and 22·3% (15·3-31·4%), respectively. Prognostic analysis of OS using a Cox multivariate model showed that factors independently associated with OS included lactate dehydrogenase ≥2 upper normal limit [hazard ratio (HR) = 2·86 (1·57-5·2), P = 0·0006]; time to failure (>6 months) [HR = 0·59 (0·36-0·97), P = 0·038]; and failure in bone marrow [HR = 2·78 (1·65-4·68), P = 0·0001]. New therapeutic strategies are required to significantly reduce refractory disease and disease relapse in patients with newly diagnosed mature B-NHL and, more importantly, there is a critical need to develop novel retrieval approaches in patients with chemotherapy-resistant disease.

摘要

我们确定了与新诊断的成熟 B 细胞非霍奇金淋巴瘤(B-NHL)患儿和青少年相关的风险因素,这些患者在法国-美国-英国成熟淋巴瘤 B(FAB/LMB)96 多药化疗期间或之后出现难治性或复发疾病。在登记的 1111 名患者中,有 104 名(9.4%)患者在首次完全缓解后出现难治性疾病或疾病复发。在这 104 名患者中,有 28 名(27%)患者出现难治性疾病,有 76 名(73%)患者出现疾病复发。估计 1 年和 2 年的总生存率(OS)(95%置信区间)分别为 31.5%(23.3-41.0%)和 22.3%(15.3-31.4%)。使用 Cox 多变量模型对 OS 的预后分析显示,与 OS 独立相关的因素包括乳酸脱氢酶≥2 个正常值上限[风险比(HR)=2.86(1.57-5.2),P=0.0006];失败时间(>6 个月)[HR=0.59(0.36-0.97),P=0.038];骨髓失败[HR=2.78(1.65-4.68),P=0.0001]。需要新的治疗策略来显著降低新诊断的成熟 B-NHL 患者的难治性疾病和疾病复发率,更重要的是,需要开发针对化疗耐药疾病的新检索方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d5/6128751/8d06d952dafa/nihms976267f1.jpg

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