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Phase II study of intensive post-remission chemotherapy and stem cell transplantation for adult acute lymphoblastic leukemia and lymphoblastic lymphoma: Japan Clinical Oncology Group Study, JCOG9402

机译:成人急性淋巴细胞白血病和淋巴母细胞淋巴瘤强化缓解后化疗和干细胞移植的II期研究:日本临床肿瘤学小组研究,JCOG9402

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Objective: To evaluate the efficacy and safety of intensive post-remission chemotherapy for untreated patients aged 15-69 years with adult acute lymphoblastic leukemia and lymphoblastic lymphoma in a multicenter Phase II study. Methods: The chemotherapy regimen consisted of induction, post-remission and maintenance for 2 years. The primary endpoint was 5-year progression-free survival, and secondary endpoints included complete remission rate, overall survival and adverse events. Among 115 patients enrolled, 108 eligible patients [median age, 33.5 years (range, 15-69)] including 96 acute lymphoblastic leukemia and 12 lymphoblastic lymphoma were assessed. Other major characteristics were male 50%, T-cell phenotype 21%, Philadelphia chromosome 22%, B-symptom+ 35% and performance status 2/3 22%. Results: Eighty-seven patients achieved complete remission (81%; 95% confidence interval 72-88%), while five (5%) died during the chemotherapy protocol. The median overall survival and progression-free survival were 1.8 years (95% confidence interval, 1.5-2.6) and 1.2 years (95% confidence interval, 0.8-1.6), respectively. Their 5-year overall survival and progression-free survival were 29 and 28%, respectively. The 5-year overall survival of 31 patients who underwent allogeneic (n= 19) or autologous (n= 12) stem cell transplantation during first complete response was 51%. Major non-hematologic toxicities of Grade 3 or greater were infections (21%) and pulmonary complications (6%). When compared with the investigators' previous Phase II trials, JCOG9402 improved progression-free survival and overall survival when compared with JCOG8702; however, it did not show improvement when compared with JCOG9004. Conclusions: Although the intensified induction and post-remission chemotherapy was feasible and 28% of the patients with adult acute lymphoblastic leukemia or lymphoblastic lymphoma achieved long-term progression-free survival, JCOG9402 did not show improvement.
机译:目的:在一项多中心II期研究中,评估强化缓解后化疗对15-69岁成人急性淋巴细胞白血病和淋巴母细胞淋巴瘤未经治疗的患者的疗效和安全性。方法:化疗方案包括诱导,缓解和维持2年。主要终点为5年无进展生存期,次要终点为完全缓解率,总体生存率和不良事件。在入组的115例患者中,评估了108例合格患者[中位年龄33.5岁(范围15-69岁)],包括96例急性淋巴细胞白血病和12例淋巴母细胞淋巴瘤。其他主要特征是男性50%,T细胞表型21%,费城染色体22%,B症状+ 35%和表现状态2/3 22%。结果:87名患者完全缓解(81%; 95%置信区间72-88%),而五名(5%)在化疗方案中死亡。中位总生存期和无进展生存期分别为1.8年(95%置信区间1.5-2.6)和1.2年(95%置信区间0.8-1.6)。他们的5年总生存率和无进展生存率分别为29%和28%。在首次完全缓解期间接受同种异体(n = 19)或自体(n = 12)干细胞移植的31名患者的5年总生存率为51%。 3级或更高级别的主要非血液学毒性是感染(21%)和肺部并发症(6%)。与研究者先前的II期临床试验相比,JCOG9402与JCOG8702相比改善了无进展生存期和总生存期。但是,与JCOG9004相比,它没有显示出改进。结论:尽管加强诱导和缓解后化疗是可行的,并且28%的成人急性淋巴细胞白血病或淋巴母细胞淋巴瘤患者可实现长期无进展生存期,但JCOG9402并未显示出改善。

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