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阿根廷一项基于柏林-法兰克福-明斯特(BFM)方案治疗儿童B细胞非霍奇金淋巴瘤和B细胞急性淋巴细胞白血病的结果。

Results of a BFM-based protocol for the treatment of childhood B-non-Hodgkin's lymphoma and B-acute lymphoblastic leukemia in Argentina.

作者信息

Chantada G L, Felice M S, Zubizarreta P A, Diaz L, Gallo G, Sackmann-Muriel F

机构信息

Hematology-Oncology Department, Hospital de Pediatría, SAMIC Prof Dr JP Garrahan, Buenos Aires, Argentina.

出版信息

Med Pediatr Oncol. 1997 May;28(5):333-41. doi: 10.1002/(sici)1096-911x(199705)28:5<333::aid-mpo2>3.0.co;2-i.

Abstract

PURPOSE

To report the feasibility and results of a study based on the BFM-ALL. NHL/86 protocol for B-non-Hodgin's Lymphoma (NHL) and B-Acute Lymphoblastic Leukemia (B-ALL) in Argentina. Design. Prospective, single arm, non-randomized trial.

PATIENTS AND METHODS

From August 1988 to December 1993, 87 consecutive patients with B-NHL/B-ALL were admitted and 82 were eligible. The therapy was stratified according to stage. All patients received a cytoreductive prephase with cyclophosphamide and prednisone. Those with stage I-II were treated with three 5-day blocks of combined intense chemotherapy including dexamethasone, cyclophosphamidie, ifosfamide, cytarabine, teniposide, doxorabicin, and 500 mg/m2 of methotrexate as a 24 hour continuous infusion. Stage III received 6 blocks and those with stage IV/B-ALL received 6 intensified blocks in which 2 g/m2 of 24 hour continuous infusion methotrexate and vincristine were added. Triple intrathecal therapy was given for CNS prevention. After the first two blocks the response was assessed and those with a partial response were offered optionallya second look surgery or local radiotherapy.

RESULTS

With a median follow-up of 38 (range 16-71) months, the event-free survival (pEFS) for the whole group was 0.69 (Stage I-II n = 16 pEFS = 0.94, stage III n = 50 pEFS = 0.66, Stage IV n = 7 pEFS = 0.43, B-ALL n = 9 pEFS = 0.66). Patients with stage III abdominal tumors who achieved a partial response by imaging studies after induction had a significantly higher risk of relapse than those with a complete response (p = 0.02). Relapse was the most frequent event Toxicity was mainly hematological.

CONCLUSIONS

The application of this protocol was feasible in our setting and its results comparable to the German study. Patients with stage I-II had an excellent outcome. Those with stage III and B-ALL achieved an encouraging event-free survival, however those with abdominal tumors and partial response to induction chemotherapy fared less favourably. This strategy was less effective for patients with initial CNS disease.

摘要

目的

报告一项基于阿根廷BFM-ALL.NHL/86方案治疗B细胞非霍奇金淋巴瘤(NHL)和B细胞急性淋巴细胞白血病(B-ALL)的研究的可行性及结果。设计:前瞻性、单臂、非随机试验。

患者与方法

1988年8月至1993年12月,连续收治87例B-NHL/B-ALL患者,82例符合条件。治疗根据分期进行分层。所有患者均接受环磷酰胺和泼尼松的细胞减灭前期治疗。I-II期患者接受三个为期5天的联合强化化疗疗程,包括地塞米松、环磷酰胺、异环磷酰胺、阿糖胞苷、替尼泊苷、多柔比星,以及24小时持续输注500mg/m²甲氨蝶呤。III期患者接受6个疗程,IV期/B-ALL患者接受6个强化疗程,其中添加2g/m² 24小时持续输注甲氨蝶呤和长春新碱。给予三联鞘内注射治疗以预防中枢神经系统受累。在前两个疗程后评估疗效,部分缓解的患者可选择进行二次探查手术或局部放疗。

结果

中位随访38(范围16 - 71)个月,全组无事件生存率(pEFS)为0.69(I-II期n = 16,pEFS = 0.94;III期n = 50,pEFS = 应改为0.66;IV期n = 7,pEFS = 0.43;B-ALL n = 9,pEFS = 0.66)。诱导治疗后影像学检查达到部分缓解的III期腹部肿瘤患者复发风险显著高于完全缓解者(p = 0.02)。复发是最常见的事件。毒性主要为血液学毒性。

结论

该方案在我们的研究环境中应用可行,其结果与德国的研究相当。I-II期患者预后良好。III期和B-ALL患者获得了令人鼓舞的无事件生存率,然而,腹部肿瘤且诱导化疗部分缓解者预后较差。该策略对初始有中枢神经系统疾病的患者效果较差。

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