Hesseling P B, Njume E, Kouya F, Katayi T, Wharin P, Tamannai M, Achu P, Kidd M, McCormick P
Department of Paediatrics and Child Health, Stellenbosch University, Tygerberg, Republic of South Africa.
Pediatr Hematol Oncol. 2012 Mar;29(2):119-29. doi: 10.3109/08880018.2011.644881.
Treatment of endemic Burkitt lymphoma (BL) with cyclophosphamide (CPM) and intrathecal methotrexate (IT MTX) can cure 50% of patients. In this study, induction therapy with CPM and IT MTX was followed by consolidation chemotherapy adapted for stage, clinical response, and abdominal ultrasound findings. One hundred and twenty-nine consecutive patients with BL, 77 male and 52 female with a median age of 7.9 years, were treated in mission hospitals in Cameroon. The diagnosis rested on fine-needle aspirate (79%), biopsy, bone marrow, cerebrospinal fluid, abdominal ultrasound, and clinical examination. Six percent had St Jude stage I, 13% stage II, 72% stage III, and 12% stage IV disease. The abdomen (76%) and face (50%) were mainly involved. Induction chemotherapy was CPM 40 mg/kg and IT MTX 12.5 mg and IT hydrocortisone 12.5 mg on days 1, 8, and 15. Stage I and II patients received CPM 60 mg/kg on day 29, and stage III patients CPM 60 mg/kg on days 29 and 43 if in remission on day 28. Stage IV patients and patients not in remission received CPM 60 mg/kg on days 29, 43, and 57 and 1.0 g/m(2) MTX intravenous (IV) and vincristine 1.5 mg/m(2) IV on day 29. Event-free survival (EFS) at mean 365 days was 61% (n = 79) and 100% in stage I, 85% in stage II, 60% in stage III, and 27% in stage IV patients. Deaths (n = 24) were disease or treatment related and 26 patients relapsed (mean 135 days). Risk-adapted treatment achieved 61% 1-year EFS.
用环磷酰胺(CPM)和鞘内注射甲氨蝶呤(IT MTX)治疗地方性伯基特淋巴瘤(BL)可治愈50%的患者。在本研究中,采用CPM和IT MTX进行诱导治疗后,根据分期、临床反应和腹部超声检查结果进行巩固化疗。129例连续的BL患者,77例男性和52例女性,中位年龄7.9岁,在喀麦隆的教会医院接受治疗。诊断依据细针穿刺抽吸(79%)、活检、骨髓、脑脊液、腹部超声和临床检查。6%为圣裘德分期I期,13%为II期,72%为III期,12%为IV期疾病。主要受累部位为腹部(76%)和面部(50%)。诱导化疗方案为第1、8和15天给予CPM 40 mg/kg、IT MTX 12.5 mg和IT氢化可的松12.5 mg。I期和II期患者在第29天给予CPM 60 mg/kg,III期患者如果在第28天缓解,则在第29天和第43天给予CPM 60 mg/kg。IV期患者和未缓解的患者在第29、43和57天给予CPM 60 mg/kg,第29天给予1.0 g/m²甲氨蝶呤静脉注射(IV)和长春新碱1.5 mg/m²静脉注射。平均365天的无事件生存率(EFS)为61%(n = 79),I期患者为100%,II期患者为85%,III期患者为60%,IV期患者为27%。死亡24例与疾病或治疗相关,26例患者复发(平均135天)。风险适应性治疗实现了61%的1年EFS。