Department of Pediatric Hematology and Immunology, Robert Debré University Hospital, AP-HP and University de Paris, Paris, France; Université de Paris, Institut Necker-Enfants Malades (INEM), Institut national de la santé et de la recherche médicale (Inserm) U1151, and Laboratory of Onco-Hematology, Assistance Publique-Hôpitaux de Paris, Hôpital Necker Enfants-Malades, Paris.
Pediatric Oncology and Hematology Department, University Hospital of Nancy (CHRU Nancy), Nancy.
Haematologica. 2022 Sep 1;107(9):2173-2182. doi: 10.3324/haematol.2021.280257.
Primary mediastinal large B-cell lymphoma (PMLBL) is a rare entity predominantly affecting adolescents and young adults. Recently, an international phase II trial in pediatric patients using dose-adjusted etoposide, doxorubicin, and cyclophosphamide with vincristine and prednisone plus rituximab (DA-EPOCH-R) failed to reproduce excellent survival reported in some adult studies. The optimal therapy regimen needs to be determined in this disease. The French prospective LMB2001 trial included all patients ≤18 years with mature B-cell lymphoma treated in French centers. For patients with PMLBL, treatment included four to eight courses of Lymphomes Malins B (LMB)-based chemotherapy without radiotherapy. From 2008, rituximab was added before each chemotherapy course. From 09/2001 to 03/2012, 42 patients with PMLBL were registered. The median age was 15 years (range, 8-18). Twenty-one patients were treated with chemotherapy plus rituximab. The median follow-up was 7.1 years (interquartile range, 5.8-11.1). Five-year event-free and overall survival were 88.1% (95% confidence interval (CI): 75.0-94.8) and 95.2% (95% CI: 84.0-98.7) for the whole population. The 5-year EFS was 81.0% (95% CI: 60.0-92.3) and 95.2% (95% CI: 77.3-99.2) (hazard ratio =0.24; 95% CI: 0.03- 2.2) and 5-year overall survival was 90.5% (95% CI: 71.1-97.3) and 100% for patients treated without and with rituximab, respectively. Only one of 21 patients treated with rituximab and LMB-based chemotherapy had local early treatment failure but achieved prolonged complete remission with second-line chemotherapy and radiotherapy. Intensive LMBbased chemotherapy with rituximab achieved excellent survival in children/adolescents with PMLBL. Further international prospective studies are required to confirm these results in this population.
原发性纵隔大 B 细胞淋巴瘤(PMLBL)是一种罕见的实体瘤,主要影响青少年和年轻成年人。最近,一项针对儿科患者的国际 II 期试验使用调整剂量的依托泊苷、多柔比星和环磷酰胺联合长春新碱和泼尼松加上利妥昔单抗(DA-EPOCH-R),未能重现一些成人研究中报道的优异生存结果。这种疾病需要确定最佳的治疗方案。法国前瞻性 LMB2001 试验纳入了所有在法国中心治疗的成熟 B 细胞淋巴瘤≤18 岁的患者。对于 PMLBL 患者,治疗包括四到八个疗程的基于 Lymphomes Malins B(LMB)的化疗,不进行放疗。从 2008 年开始,在每个化疗疗程前添加利妥昔单抗。从 2001 年 9 月至 2012 年 3 月,登记了 42 例 PMLBL 患者。中位年龄为 15 岁(范围,8-18 岁)。21 例患者接受化疗加利妥昔单抗治疗。中位随访时间为 7.1 年(四分位距,5.8-11.1)。全人群的 5 年无事件生存率和总生存率分别为 88.1%(95%可信区间(CI):75.0-94.8)和 95.2%(95%CI:84.0-98.7)。5 年无事件生存率为 81.0%(95%CI:60.0-92.3)和 95.2%(95%CI:77.3-99.2)(风险比=0.24;95%CI:0.03-2.2),而未接受和接受利妥昔单抗治疗的患者 5 年总生存率分别为 90.5%(95%CI:71.1-97.3)和 100%。21 例接受利妥昔单抗和 LMB 为基础的化疗的患者中,仅有 1 例出现局部早期治疗失败,但通过二线化疗和放疗获得了延长的完全缓解。强化 LMB 为基础的化疗联合利妥昔单抗可使 PMLBL 患儿/青少年获得优异的生存结果。需要进一步的国际前瞻性研究来证实这一人群的结果。