Department of Paediatric Haematology, Oncology and Palliative Care, Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital, Cambridge, United Kingdom.
Department of Pediatric and Adolescent Oncology, INSERM 1015, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
J Clin Oncol. 2021 Nov 20;39(33):3716-3724. doi: 10.1200/JCO.21.00920. Epub 2021 Sep 27.
A dose-adjusted etoposide, doxorubicin, and cyclophosphamide with vincristine and prednisone plus rituximab (DA-EPOCH-R) regimen has been shown to deliver excellent survival for adults with primary mediastinal large B-cell lymphoma (PMLBL) without the use of radiotherapy. No international prospective evaluation of this regimen has previously been reported in children and adolescents.
We conducted an international single-arm phase II trial involving patients younger than age 18 years with PMLBL who were to receive six courses of DA-EPOCH-R. The primary end point was event-free survival (EFS). Overall survival and toxicity were also assessed. This trial was registered (ClinicalTrials.gov identifier: NCT01516567).
Analyses were based on 46 patients. The median age was 15.4 years (interquartile range: 14-16 years). The median follow-up was 59.0 months (interquartile range: 52.6-69.2 months). Fourteen events were observed (eight relapses or progressions (including three parenchymal CNS relapses), four residual lymphoma, and two second malignancies). The 4-year EFS was 69.6% (95% CI, 55.2 to 80.9), which did not differ from the rate observed historically ( = .59). Seven deaths occurred (six disease-related and one second malignancy). The overall survival was 84.8% (95% CI, 71.8 to 92.4). Twenty-two patients (48%) reached dose levels ≥ 4. Nonhematologic adverse events grade ≥ 3 or cardiac adverse events grade ≥ 2 occurred in 47 of 276 (17%) courses and 30 of 46 patients (65%).
DA-EPOCH-R did not improve the EFS compared with a historical control in this first prospective multisite international study of children and adolescents with PMLBL. Further studies are required to determine the optimum therapy for children and adolescents with this lymphoma.
已证实,对于原发性纵隔大 B 细胞淋巴瘤(PMLBL)成人患者,采用依托泊苷、多柔比星、环磷酰胺联合长春新碱和泼尼松加利妥昔单抗(DA-EPOCH-R)的剂量调整方案可显著提高生存率,而无需放疗。此前,尚未有国际前瞻性评估该方案在儿童和青少年中的应用。
我们开展了一项国际性、单臂、Ⅱ期临床试验,纳入了年龄小于 18 岁的 PMLBL 患者,他们将接受六个疗程的 DA-EPOCH-R 治疗。主要终点为无事件生存率(EFS)。同时评估总生存率和毒性。该试验已在 ClinicalTrials.gov 注册(注册号:NCT01516567)。
基于 46 例患者进行了分析。中位年龄为 15.4 岁(四分位距:14-16 岁)。中位随访时间为 59.0 个月(四分位距:52.6-69.2 个月)。观察到 14 例事件(8 例复发或进展(包括 3 例实质 CNS 复发),4 例残留淋巴瘤,2 例第二恶性肿瘤)。4 年 EFS 为 69.6%(95%CI:55.2-80.9),与历史观察结果无差异( =.59)。7 例死亡(6 例与疾病相关,1 例与第二恶性肿瘤相关)。总生存率为 84.8%(95%CI:71.8-92.4)。22 例患者(48%)达到了剂量水平≥4。276 个疗程中共有 47 个(17%)和 46 例患者中的 30 个(65%)出现了≥3 级非血液学不良事件或≥2 级心脏不良事件。
在这项针对 PMLBL 儿童和青少年的首次前瞻性多中心国际研究中,与历史对照相比,DA-EPOCH-R 并未改善 EFS。需要进一步研究以确定该淋巴瘤患儿和青少年的最佳治疗方案。