De Botton S, Dombret H, Sanz M, Miguel J S, Caillot D, Zittoun R, Gardembas M, Stamatoulas A, Condé E, Guerci A, Gardin C, Geiser K, Makhoul D C, Reman O, de la Serna J, Lefrere F, Chomienne C, Chastang C, Degos L, Fenaux P
Service d'Hematologie of the Centre Hospitalier Universitaire (CHU) of Lille, France.
Blood. 1998 Oct 15;92(8):2712-8.
All trans-retinoic acid (ATRA) syndrome is a life-threatening complication of uncertain pathogenesis that can occur during the treatment of acute promyelocytic leukemia (APL) by ATRA. Since its initial description, however, no large series of ATRA syndrome has been reported in detail. We analyzed cases of ATRA syndrome observed in an ongoing European trial of treatment of newly diagnosed APL. In this trial, patients 65 years of age or less with an initial white blood cell count (WBC) less than 5,000/microL were initially randomized between ATRA followed by chemotherapy (CT) (ATRA-->CT group) or ATRA with CT started on day 3; patients with WBC greater than 5,000/microL received ATRA and CT from day 1; patients aged 66 to 75 received ATRA-->CT. In patients with initial WBC less than 5, 000/microL and allocated to ATRA-->CT, CT was rapidly added if WBC was greater than 6,000, 10,000, 15,000/microL by days 5, 10, and 15 of ATRA treatment. A total of 64 (15%) of the 413 patients included in this trial experienced ATRA syndrome during induction treatment. Clinical signs developed after a median of 7 days (range, 0 to 35 days). In two of them, they were in fact present before the onset of ATRA. In 11 patients, they occurred upon recovery from the phase of aplasia due to the addition of CT. Respiratory distress (89% of the patients), fever (81%), pulmonary infiltrates (81%), weight gain (50%), pleural effusion (47%), renal failure (39%), pericardial effusion (19%), cardiac failure (17%), and hypotension (12%) were the main clinical signs, and 63 of the 64 patients had at least three of them. Thirteen patients required mechanical ventilation and two dialysis. A total of 60 patients received CT in addition to ATRA as per protocol or based on increasing WBC; 58 also received high dose dexamethasone (DXM); ATRA was stopped when clinical signs developed in 30 patients. A total of 55 patients (86%) who experienced ATRA syndrome achieved complete remission (CR), as compared with 94% of patients who had no ATRA syndrome (P = .07) and nine (14%) died of ATRA syndrome (5 cases), sepsis (2 cases), leukemic resistance (1 patient), and central nervous system (CNS) bleeding (1 patient). None of the patients who achieved CR and received ATRA for maintenance had ATRA syndrome recurrence. No significant predictive factors of ATRA syndrome, including pretreatment WBC, could be found. Kaplan Meier estimates of relapse, event-free survival (EFS), and survival at 2 years were 32% +/- 10%, 63% +/- 8%, and 68% +/- 7% in patients who had ATRA syndrome as compared with 15% +/- 3%, 77% +/- 2%, and 80% +/- 2% in patients who had no ATRA syndrome (P = .05, P = .003, and P = .03), respectively. In a stepwise Cox model that also included pretreatment prognostic variables, ATRA syndrome remained predictive for EFS and survival. In conclusion, in this multicenter trial where CT was rapidly added to ATRA in case of high or increasing WBC counts and DXM generally also used at the earliest clinical sign, the incidence of ATRA syndrome was 15%, but ATRA syndrome was responsible for death in only 1.2% of the total number of patients treated. However, occurrence of ATRA syndrome was associated with lower EFS and survival.
全反式维甲酸(ATRA)综合征是一种发病机制不明的危及生命的并发症,可发生于用ATRA治疗急性早幼粒细胞白血病(APL)的过程中。然而,自其首次被描述以来,尚无关于ATRA综合征的大量病例系列被详细报道。我们分析了在一项正在进行的欧洲新诊断APL治疗试验中观察到的ATRA综合征病例。在该试验中,65岁及以下、初始白细胞计数(WBC)低于5000/微升的患者最初被随机分为接受ATRA后化疗(CT)(ATRA→CT组)或在第3天开始使用ATRA联合CT;WBC大于5000/微升的患者从第1天起接受ATRA和CT;66至75岁的患者接受ATRA→CT。对于初始WBC低于5000/微升且被分配到ATRA→CT组的患者,如果在ATRA治疗的第5、10和15天WBC大于6000、10000、15000/微升,则迅速加用CT。该试验纳入的413例患者中,共有64例(15%)在诱导治疗期间发生了ATRA综合征。临床症状在中位7天(范围0至35天)后出现。其中2例实际上在ATRA开始前就已存在症状。11例患者在因加用CT导致的再生障碍期恢复时出现症状。呼吸窘迫(89%的患者)、发热(81%)、肺部浸润(81%)、体重增加(50%)、胸腔积液(47%)、肾衰竭(39%)、心包积液(19%)、心力衰竭(17%)和低血压(12%)是主要临床症状,64例患者中有63例至少出现其中三种症状。13例患者需要机械通气,2例需要透析。共有60例患者按照方案或根据WBC升高情况在接受ATRA的基础上加用了CT;58例还接受了高剂量地塞米松(DXM);30例患者出现临床症状时停用了ATRA。发生ATRA综合征的55例患者(86%)实现了完全缓解(CR),未发生ATRA综合征的患者为94%(P = 0.07),9例(14%)死于ATRA综合征(5例)、败血症(2例)、白血病耐药(1例)和中枢神经系统(CNS)出血(1例)。所有实现CR并接受ATRA维持治疗的患者均未出现ATRA综合征复发。未发现包括治疗前WBC在内的ATRA综合征的显著预测因素。发生ATRA综合征的患者2年时的复发、无事件生存(EFS)和生存的Kaplan Meier估计值分别为32%±10%、63%±8%和68%±7%,而未发生ATRA综合征的患者分别为15%±3%、77%±2%和80%±2%(P = 0.05、P = 0.003和P = 0.03)。在一个也包括治疗前预后变量的逐步Cox模型中,ATRA综合征仍然是EFS和生存的预测因素。总之,在这项多中心试验中,如果WBC计数高或升高则迅速在ATRA基础上加用CT,并且通常在最早出现临床症状时就使用DXM,ATRA综合征的发生率为15%,但ATRA综合征仅导致1.2%的总治疗患者死亡。然而,ATRA综合征的发生与较低的EFS和生存率相关。