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首页> 外文期刊>Japanese journal of clinical oncology. >Long-term follow-up results of adult patients with acute lymphocytic leukemia or lymphoblastic lymphoma treated with short-term, alternating non-cross-resistant chemotherapy: Japan Clinical Oncology Group Study 8702. Lymphoma Study Group.
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Long-term follow-up results of adult patients with acute lymphocytic leukemia or lymphoblastic lymphoma treated with short-term, alternating non-cross-resistant chemotherapy: Japan Clinical Oncology Group Study 8702. Lymphoma Study Group.

机译:成人急性淋巴细胞白血病或淋巴母细胞淋巴瘤患者短期,交替,非交叉耐药的化疗方案的长期随访结果:日本临床肿瘤学研究8702。淋巴瘤研究组。

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BACKGROUND: Patients with acute lymphocytic leukemia (ALL) and those with lymphoblastic lymphoma (LBL) have overlapping clinical and immunophenotypic features and they have been treated with the same or very similar chemotherapy regimens. The goal of this multi-institutional phase II trial was to evaluate the therapeutic efficacy of a short-term, six-drug chemotherapy regimen for adult patients with untreated ALL or LBL. METHODS: Forty-six eligible patients, 41 with ALL and five with LBL, were treated with a short-term (planned total therapy duration; 36-38 weeks), simplified chemotherapy program; two courses of VEPA-L (vincristine, cyclophosphamide, prednisolone, doxorubicin, I-asparaginase plus intrathecal methotrexate and prednisolone) followed by four courses of M-VEPA (methotrexate plus VEPA), without the traditional maintenance therapy using daily 6-mercaptopurine and weekly methotrexate. RESULTS: Thirty-six (78%; 95% confidence interval 64-89%) of the 46 eligible patients achieved complete remission (CR). Among the 36 patients who achieved CR, four (11%) died of treatment complications, 26 (72%) relapsed and six (17%) remain alive in continuous CR. The median survival for all 46 eligible patients is 14 months and the median disease-free survival (DFS) for the 36 patients who achieved CR is 11 months. The estimate of the proportion of survival at 7 years of all 46 eligible patients is 15% at a median follow-up time of 96 months and that of DFS of the 36 patients achieving CR is 17% at a median follow-up time of 93 months. Subgroup analysis showed that an elevated serum C-reactive protein (CRP) level, age of 30 years or older, the presence of B-symptom and T-cell phenotype were likely to be associated with shortened survival. Although the observed CR rate (78%) is within the range of satisfaction, the long-term survival rate (15%) is inferior to those of published programs incorporating maintenance therapy. CONCLUSIONS: A fraction of adult patients with ALL or LBL are curable with a short-term, six-drug chemotherapy regimen. However, this simplified therapy of shorter duration cannot be recommended.
机译:背景:急性淋巴细胞性白血病(ALL)和淋巴母细胞性淋巴瘤(LBL)患者具有重叠的临床和免疫表型特征,并已接受相同或非常相似的化疗方案治疗。这项多机构II期试验的目标是评估短期六药化疗方案对未经治疗的ALL或LBL成年患者的治疗效果。方法:46例符合条件的患者,其中41例ALL,5例LBL,接受短期(计划总治疗时间; 36-38周)简化化疗方案治疗; 2个疗程的VEPA-L(长春新碱,环磷酰胺,泼尼松龙,阿霉素,I-天冬酰胺酶加鞘内甲氨蝶呤和泼尼松龙),然后是4个疗程的M-VEPA(甲氨蝶呤加VEPA),而没有采用每天6-巯基嘌呤和每周一次的传统维持疗法甲氨蝶呤。结果:46名符合条件的患者中有36名(78%; 95%置信区间64-89%)达到了完全缓解(CR)。在36例获得CR的患者中,有4例(11%)死于治疗并发症,有26例(72%)复发,还有6例(17%)在持续CR中存活。所有46名合格患者的中位生存期为14个月,而获得CR的36例患者的中位无病生存期(DFS)为11个月。在平均随访时间为96个月的情况下,所有46名合格患者在7年生存率的估计为15%,在平均随访时间为93的36位获得CR的患者中,DFS估计为17%。几个月。亚组分析显示,血清C反应蛋白(CRP)水平升高,年龄大于或等于30岁,B症状和T细胞表型的存在可能与生存期缩短有关。尽管观察到的CR率(78%)在满意范围内,但长期存活率(15%)低于已发布的采用维持治疗的计划。结论:一小部分成人ALL或LBL患者可通过短期六药化疗方案治愈。但是,不推荐这种持续时间较短的简化疗法。

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