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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Improving acute promyelocytic leukemia (APL) outcome in developing countries through networking, results of the International Consortium on APL.
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Improving acute promyelocytic leukemia (APL) outcome in developing countries through networking, results of the International Consortium on APL.

机译:通过网络,国际财团的结果改善发展中国家的急性早野白血病(APL)结果。

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Thanks to modern treatment with all-trans retinoic acid and chemotherapy, acute promyelocytic leukemia (APL) is now the most curable type of leukemia. However, this progress has not yielded equivalent benefit in developing countries. The International Consortium on Acute Promyelocytic Leukemia (IC-APL) was established to create a network of institutions in developing countries that would exchange experience and data and receive support from well-established US and European cooperative groups. The IC-APL formulated expeditious diagnostic, treatment, and supportive guidelines that were adapted to local circumstances. APL was chosen as a model disease because of the potential impact on improved diagnosis and treatment. The project included 4 national coordinators and reference laboratories, common clinical record forms, 5 subcommittees, and laboratory and data management training programs. In addition, participating institutions held regular virtual and face-to-face meetings. Complete hematological remission was achieved in 153/180 (85%) patients and 27 (15%) died during induction. After a median follow-up of 28 months, the 2-year cumulative incidence of relapse, overall survival (OS), and disease-free survival (DFS) were 4.5%, 80%, and 91%, respectively. The establishment of the IC-APL network resulted in a decrease of almost 50% in early mortality and an improvement in OS of almost 30% compared with historical controls, resulting in OS and DFS similar to those reported in developed countries.
机译:由于具有全反式视黄酸和化疗的现代化治疗,急性幼幼细胞白血病(APL)现在是最具可治愈的白血病类型。但是,这一进展在发展中国家尚未产生相同的利益。建立了国际联合急性临突细胞癌白血病(IC-APL),为发展中国家建立了一家交流经验和数据的机构网络,并从成熟的美国和欧洲合作团体获得支持。 IC-APL制定迅速的诊断,治疗和支持准则,适应当地情况。选择APL作为模型疾病,因为对改善诊断和治疗的潜在影响。该项目包括4个国家协调员和参考实验室,常见的临床记录表,5个小组委员会和实验室和数据管理培训计划。此外,参与机构定期持有虚拟和面对面的会议。在153/180(85%)患者中,在诱导期间死亡,27例(15%)达到完整的血液治疗。 28个月中间后续后续后,复发的2年累积发病率,总存活(OS)和无病生存率(DFS)分别为4.5%,80%和91%。 IC-APL网络的建立导致近50%的早期死亡率降低,与历史对照相比,OS的改善,近30%,导致OS和DFS类似于发达国家报告的OS和DF。

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