首页> 外文期刊>Leukemia and lymphoma >Results of a randomized phase III trial in children and adolescents with advanced stage diffuse large cell non-Hodgkin's lymphoma: a Pediatric Oncology Group study.
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Results of a randomized phase III trial in children and adolescents with advanced stage diffuse large cell non-Hodgkin's lymphoma: a Pediatric Oncology Group study.

机译:晚期弥漫性大细胞非霍奇金淋巴瘤的儿童和青少年的III期随机试验结果:小儿肿瘤小组研究。

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PURPOSE: The Pediatric Oncology Group (POG) adopted a histology-based approach to the management of pediatric non-Hodgkin's lymphomas (NHL) utilizing the National Cancer Institute Working Formulation for Clinical Usage. Patients with diffuse large cell lymphoma (DLCL) were treated on a separate protocol from small cell diffuse undifferentiated or lymphoblastic lymphomas. This study assessed the overall and event free survival of children with DLCL and determined the effects of cyclophosphamide upon these end-points in a prospective randomized trial. PATIENTS AND METHODS: One hundred and twenty eligible stage III or IV NHL patients with the confirmed diagnosis of diffuse large cell or immunoblastic histology were enrolled on study between October 1986 and November 1991. Patients were randomized to receive or not receive cyclophosphamide: 58 received cyclophosphamide, doxorubicin, vincristine, 6-mercaptopurine (6-MP), and prednisone (ACOP+) and 62 were treated with doxorubicin, vincristine, 6-MP, and prednisone (APO). In both treatment programs methotrexate was substituted when the doxorubicin cumulative dose reached 450 mg/m2. Radiation was administered to bulky disease if progression or no response were observed after induction therapy. Planned duration of therapy was 12 months. RESULTS: The 5-year event free survival (EFS) rates of patients treated with ACOP+ versus APO were 62+/-7 and 72+/-6%, respectively. While there was no statistically significant difference between the two treatment arms (p = 0.28), we can only say that we are 95% confident that the difference in 5-year EFS falls in the wide range from 28% in favor of APO to 8% favoring ACOP+. Marrow suppression was the main toxicity with one fatal infection. There were three other deaths on study due to respiratory failure in patients with mediastinal masses. Only one patient experienced cardiotoxicity requiring discontinuation of doxorubicin. Ten patients received radiation therapy to achieve remission. CONCLUSION: The efficacy of elimination of cyclophosphamide from the treatment program of children and adolescents with advanced stage diffuse large cell lymphoma was inconclusive as to its effect on EFS. Furthermore, the majority of the patients (92%) did not require any radiation therapy to bulky disease indicating that the chemotherapy regimens are quite efficient for achievement of complete remission.
机译:目的:儿科肿瘤学组(POG)采用了一种基于组织学的方法来利用美国国家癌症研究所临床用药配方来管理小儿非霍奇金淋巴瘤(NHL)。弥漫性大细胞淋巴瘤(DLCL)患者与小细胞弥散性未分化或淋巴母细胞性淋巴瘤分开治疗。这项研究在一项前瞻性随机试验中评估了DLCL儿童的总体生存率和无事件生存率,并确定了环磷酰胺对这些终点的影响。患者和方法:1986年10月至1991年11月,共入选了120例经确诊为弥漫性大细胞或免疫母细胞组织学的合格的III或IV期NHL患者。患者随机接受或不接受环磷酰胺治疗:58例接受环磷酰胺治疗,阿霉素,长春新碱,6-巯基嘌呤(6-MP)和泼尼松(ACOP +)和62用阿霉素,长春新碱,6-MP和泼尼松(APO)处理。在两种治疗方案中,当阿霉素累积剂量达到450 mg / m2时,都会用甲氨蝶呤替代。如果诱导治疗后观察到进展或无反应,则对大块疾病进行放射治疗。计划的治疗时间为12个月。结果:ACOP +相对于APO治疗的5年无事件生存率(EFS)分别为62 +/- 7和72 +/- 6%。虽然两个治疗组之间没有统计学上的显着差异(p = 0.28),但我们只能说我们有95%的信心认为5年EFS的差异在28%的支持APO到8%的宽泛范围内%赞成ACOP +。骨髓抑制是一种致命感染的主要毒性。纵隔包块患者中还有3例因呼吸衰竭而死亡。只有一名患者出现心脏毒性,需要停用阿霉素。十名患者接受了放射治疗以实现缓解。结论:从儿童和青少年晚期弥漫性大细胞淋巴瘤的治疗方案中消除环磷酰胺的疗效尚无定论。此外,大多数患者(92%)不需要对大块疾病进行任何放射治疗,这表明化学疗法对于完全缓解非常有效。

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