Division of Hematology, Shiga University of Medical Science, Seta Tsukinowa-cho, Otsu, Shiga, 520-2192, Japan.
Hematology, Saiseikai Yokohama Nanbu Hospital, Yokohama, Japan.
Ann Hematol. 2020 Dec;99(12):2787-2800. doi: 10.1007/s00277-020-04245-6. Epub 2020 Sep 2.
Significant advancements have been achieved with regard to the outcomes of acute promyelocytic leukemia (APL) patients through the introduction of all-trans retinoic acid; however, early hemorrhagic death and differentiation syndrome remain the major causes of remission induction failure in patients with APL. To investigate early death, serious hemorrhage, and differentiation syndrome during remission induction therapy in terms of incidence, risk factors, influence on outcomes, and prophylactic effects of several new anticoagulants, the results of 344 patients enrolled in the Acute Promyelocytic Leukemia 204 study conducted by the Japan Adult Leukemia Study Group were analyzed. Early death was observed in 16 patients (4.7%), of whom 14 had serious hemorrhage and 2 had differentiation syndrome. Serious hemorrhage and differentiation syndrome of grade 2 or higher were observed in 21 and 54 patients, respectively. Patients who achieved complete remission had a 7-year disease-free survival of 84.8% if they did not experience serious hemorrhage and 40.0% if they experienced serious hemorrhage during remission induction therapy (P = 0.001). Risk factor analyses showed that higher white blood cell count was associated with early death, higher white blood cell count and lower platelet count with serious hemorrhage, and leukocytosis during induction therapy and higher body surface area with differentiation syndrome. In conclusion, these results indicate that patients with such high-risk features may benefit from more intensive supportive care. The hemorrhagic risk was not relieved by the introduction of new anticoagulants. Further studies are required to establish the predictive impact of body surface area on differentiation syndrome. This trial is registered with UMIN-CTR as C000000154 on September 13, 2005.
通过引入全反式维甲酸,急性早幼粒细胞白血病(APL)患者的治疗结果取得了显著进展;然而,早期出血性死亡和分化综合征仍然是 APL 患者诱导缓解失败的主要原因。为了研究诱导缓解治疗期间早期死亡、严重出血和分化综合征的发生率、危险因素、对结局的影响以及几种新型抗凝剂的预防效果,分析了日本成人白血病研究组进行的急性早幼粒细胞白血病 204 研究中纳入的 344 例患者的结果。16 例(4.7%)患者发生早期死亡,其中 14 例发生严重出血,2 例发生分化综合征。21 例和 54 例患者分别发生 2 级或更高级别的严重出血和分化综合征。未发生严重出血的患者完全缓解后 7 年无病生存率为 84.8%,而发生严重出血的患者为 40.0%(P = 0.001)。风险因素分析表明,较高的白细胞计数与早期死亡相关,较高的白细胞计数和较低的血小板计数与严重出血相关,诱导治疗期间白细胞增多和较高的体表面积与分化综合征相关。总之,这些结果表明,具有此类高危特征的患者可能受益于更强化的支持性治疗。新型抗凝剂的引入并未减轻出血风险。需要进一步的研究来确定体表面积对分化综合征的预测影响。该试验于 2005 年 9 月 13 日在 UMIN-CTR 注册为 C000000154。