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首页> 外文期刊>Seminars in Thrombosis and Hemostasis >Long-term incidence of hematological evolution in three French prospective studies of hydroxyurea and pipobroman in polycythemia vera and essential thrombocythemia
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Long-term incidence of hematological evolution in three French prospective studies of hydroxyurea and pipobroman in polycythemia vera and essential thrombocythemia

机译:在法国的三项前瞻性研究中,羟基尿素和pibrobroman在真性红细胞增多症和原发性血小板增多症中血液学演变的长期发生率

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摘要

Despite recent discoveries made in myeloproliferative disorders other than chronic myelogenous leukemia, which it is hoped will result in earlier diagnosis, and better evaluation and management of patients, hematological evolution to myelofibrosis, acute leukemia, and myelodysplastic syndromes (AL/MDS) remain major causes of long-term mortality in polycythemia vera (PV) and essential thrombocythemia (ET) patients. Evaluation of long-term leukemogenic risk of currently available drugs, therefore, is crucial. We report updated results of three French prospective trials of hydroxyurea and pipobroman in PV and ET patients with a median follow-up longer than 10 years. The results show that the incidence of AL/MDS is higher than previously reported with no evidence of a plateau (with ~40% of AL/MDS cases occurring after the 12th year of follow-up). Although hydroxyurea currently remains the first choice in the treatment of high-risk PV and ET patients, the use of nonleukemogenic drugs, such as interferon α(IFN-α) or anagrelide, should be assessed more widely in randomized trials using accurate diagnostic criteria and taking into account the presence of the JAK2 mutation, given that they may have an impact on disease evolution. Copyright 2006 by Thieme Medical Publishers, Inc.
机译:尽管最近发现了除慢性粒细胞性白血病以外的其他骨髓增生性疾病,但希望能导致更早的诊断,更好的患者评估和治疗,骨髓纤维化,急性白血病和骨髓增生异常综合症(AL / MDS)的血液学演变真性红细胞增多症(PV)和原发性血小板增多症(ET)患者的长期死亡率。因此,评估现有药物的长期致白血病风险至关重要。我们报告了对中位随访期超过10年的PV和ET患者进行的三项法国羟基脲和pipobroman前瞻性试验的最新结果。结果表明,AL / MDS的发生率比以前报道的高,没有任何平稳期的证据(约有40%的AL / MDS病例在随访的第12年后发生)。尽管羟基脲目前仍是高危PV和ET患者的首选治疗方法,但在随机试验中应使用准确的诊断标准和更广泛的方法评估非白血病药物的使用,例如干扰素α(IFN-α)或阿那格雷等。考虑到JAK2突变的存在,因为它们可能会对疾病的发展产生影响。 Thieme Medical Publishers,Inc.版权所有2006。

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