Collins A J, Bloomfield C D, Peterson B A, McKenna R W, Edson J R
Arch Intern Med. 1978 Nov;138(11):1677-80. doi: 10.1001/archinte.138.11.1677.
Seven adults with acute promyelocytic leukemia (APL) and disseminated intravascular coagulation were treated for remission induction with daunorubicin hydrochloride and prednisone. In all patients the coagulopathy was managed with continuous-infusion heparin sodium and vigorous transfusion with platelets, cryoprecipitate, and fresh frozen plasma. Five patients survived induction; they all achieved complete remission (CR). Median duration of CR was 27 + months; two patients presently survive in their initial CR at 28 and 48 months. Recognition of APL as a distinct type of acute leukemia and prompt initiation of treatment aimed at rapid cytoreduction and control of the coagulopathy has resulted in a prolonged disease-free survival for the majority of patients.
七名患有急性早幼粒细胞白血病(APL)并伴有弥散性血管内凝血的成人患者,接受了盐酸柔红霉素和泼尼松诱导缓解治疗。所有患者的凝血病均采用持续输注肝素钠,并积极输注血小板、冷沉淀和新鲜冰冻血浆进行处理。五名患者诱导治疗后存活;他们均实现了完全缓解(CR)。CR的中位持续时间为27 + 个月;两名患者目前在初次CR状态下分别存活28个月和48个月。将APL识别为一种独特类型的急性白血病,并迅速启动旨在快速细胞减少和控制凝血病的治疗,已使大多数患者实现了延长的无病生存期。