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土耳其两个中心儿童急性淋巴细胞白血病的长期结果:ALL-BFM 95方案15年的经验

The long-term results of childhood acute lymphoblastic leukemia at two centers from Turkey: 15 years of experience with the ALL-BFM 95 protocol.

作者信息

Güneş Adalet Meral, Oren Hale, Baytan Birol, Bengoa Sebnem Yılmaz, Evim Melike Sezgin, Gözmen Salih, Tüfekçi Ozlem, Karapınar Tuba Hilkay, Irken Gülersu

机构信息

Department of Pediatric Hematology, Faculty of Medicine, Uludağ University, Bursa, Turkey.

出版信息

Ann Hematol. 2014 Oct;93(10):1677-84. doi: 10.1007/s00277-014-2106-0. Epub 2014 May 27.

Abstract

Dramatic progress in the treatment of childhood acute lymphoblastic leukemia (ALL) has been achieved during the last two decades in Western countries, where the 5-year event-free survival (EFS) rate has risen from 30 to 85 %. However, similarly high cure rates have not always been achieved in all centers in developing countries due to limited sources. We evaluated the treatment results of the ALL-Berlin-Frankfurt-Münster (BFM) 95 protocol as used between 1995 and 2009 in the pediatric hematology departments of two university hospitals. A retrospective analysis of 343 children newly diagnosed with ALL (M/F 200/143, median age 6.8 years) was performed. The overall survival (OS) and EFS according to age, initial leukocyte count, immunophenotype, chemotherapy responses (on days 8, 15, and 33), and risk groups were analyzed by Kaplan-Meier survival analysis. Median follow-up time was 6.4 years. Complete remission was achieved in 97 % of children. Five-year EFS and OS were found to be 78.4 and 79.9 %, respectively. Children younger than 6 years old had significantly better EFS and OS (83.7 and 85.2 %) than children aged ≥6 years (71.4 and 72.8 %). Adolescents achieved 63 % EFS and 65 % OS. Patients who had initial leukocyte counts of <20 × 10(9)/L had better EFS and OS (82.2 and 84.6 %) than children with higher initial leukocyte counts (72.6 and 72.6 %). EFS for B-cell precursor and T-cell ALL was 81.5 and 66.7 %, respectively. Children with a good response to prednisolone on day 8 (87 %) achieved significantly better EFS and OS (81.2 and 81.9 % vs. 55.3 and 60.5 %). Children whose bone marrow on day 15 was in complete remission had higher EFS and OS (83.7 and 86.6.1 % vs. 56.4 and 61.5 %). Children in the standard-risk and medium-risk groups obtained statistically significantly higher EFS (95.5 and 82.7 %) and OS (97.7 and 82.3 %) compared to the high-risk group (EFS 56.3 %, OS 63.4 %). The relapse rate was 14.8 %. The median relapse time from diagnosis was 23.2 months. Death occurred in 69 of 343 patients (20.1 %). The major causes of death were infection and relapse. None of the patients died of drug-related toxicity. The ALL-BFM 95 protocol was applied successfully in these two centers. In developing countries in which minimal residual disease cannot be monitored, this protocol can still be used with high survival rates.

摘要

在过去二十年里,西方国家在儿童急性淋巴细胞白血病(ALL)的治疗方面取得了显著进展,其5年无事件生存率(EFS)从30%提高到了85%。然而,由于资源有限,发展中国家并非所有中心都能达到如此高的治愈率。我们评估了1995年至2009年间在两家大学医院儿科血液科使用的ALL-柏林-法兰克福-明斯特(BFM)95方案的治疗结果。对343例新诊断为ALL的儿童(男/女200/143,中位年龄6.8岁)进行了回顾性分析。通过Kaplan-Meier生存分析,根据年龄、初始白细胞计数、免疫表型、化疗反应(第8、15和33天)以及风险组分析总生存(OS)和EFS。中位随访时间为6.4年。97%的儿童实现了完全缓解。5年EFS和OS分别为78.4%和79.9%。6岁以下儿童的EFS和OS(83.7%和85.2%)显著优于6岁及以上儿童(71.4%和72.8%)。青少年的EFS为63%,OS为65%。初始白细胞计数<20×10⁹/L的患者的EFS和OS(82.2%和84.6%)优于初始白细胞计数较高的儿童(72.6%和72.6%)。B细胞前体ALL和T细胞ALL的EFS分别为81.5%和66.7%。第8天对泼尼松龙反应良好的儿童(87%)的EFS和OS显著更好(81.2%和81.9%,而分别为55.3%和60.5%)。第15天骨髓完全缓解的儿童的EFS和OS更高(83.7%和86.6%,而分别为56.4%和61.5%)。与高危组(EFS 56.3%,OS 63.4%)相比,标准风险组和中风险组的儿童获得了统计学上显著更高的EFS(95.5%和82.7%)和OS(97.7%和82.3%)。复发率为14.8%。从诊断开始的中位复发时间为23.2个月。343例患者中有69例死亡(20.1%)。主要死亡原因是感染和复发。没有患者死于药物相关毒性。ALL-BFM 95方案在这两个中心成功应用。在无法监测微小残留病的发展中国家,该方案仍可用于实现高生存率。

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