Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Br J Haematol. 2014 Apr;165(1):102-11. doi: 10.1111/bjh.12736. Epub 2014 Jan 15.
To improve long-term outcomes for Burkitt leukaemia/lymphoma (BL) or aggressive lymphomas in adults, we assessed the benefit of adding rituximab and filgrastim support to a dose-dense modified chemotherapy regimen from the Cancer and Leukemia Group B (CALGB) 9251 trial. One hundred and five patients (aged 19-79 years) were enrolled; 27% were >60 years old; 47% had high or high-intermediate risk by International Prognostic Index (IPI) criteria. Common severe toxicities included stomatitis/upper gastrointestinal toxicity (69%), renal insufficiency (10%), neurological events (25%) and pulmonary events (18%). Seven died from treatment-related causes (one central nervous system bleed, four infections, two respiratory failure); five were >60 years old. Results in this adult population are encouraging as complete response (CR) was observed in 83% and 4-year event-free (EFS) and overall survivals (OS) were 74% and 78%, respectively. Results compare favourably to our prior chemotherapy alone study (CALGB 9251) but despite this, high-risk patients still had worse outcomes. In conclusion, short duration, intensive chemo-immunotherapy is feasible and should be considered in adults with BL as it results in high remission rates and durable remissions.
为了改善伯基特白血病/淋巴瘤(BL)或成人侵袭性淋巴瘤的长期预后,我们评估了在癌症和白血病组 B(CALGB)9251 试验中的剂量密集改良化疗方案中添加利妥昔单抗和非格司亭支持的益处。共纳入 105 例患者(年龄 19-79 岁);27%的患者年龄>60 岁;47%的患者按国际预后指数(IPI)标准属于高危或中高危。常见的严重毒性包括口腔炎/上消化道毒性(69%)、肾功能不全(10%)、神经事件(25%)和肺部事件(18%)。7 例患者死于治疗相关原因(1 例中枢神经系统出血,4 例感染,2 例呼吸衰竭);5 例患者年龄>60 岁。该成年人群的结果令人鼓舞,完全缓解(CR)率为 83%,4 年无事件生存(EFS)和总生存(OS)率分别为 74%和 78%。结果与我们之前单独化疗的研究(CALGB 9251)相比更为有利,但尽管如此,高危患者的结局仍较差。总之,短疗程、强化化疗免疫治疗是可行的,并且应该在 BL 成人患者中考虑使用,因为它可以带来高缓解率和持久缓解。