Slats A M, Egeler R M, van der Does-van den Berg A, Korbijn C, Hählen K, Kamps W A, Veerman A J P, Zwaan C M
Department of Pediatric Hematology/Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Leukemia. 2005 Apr;19(4):537-44. doi: 10.1038/sj.leu.2403665.
We analyzed causes of death, other than resistant disease or relapse, in 875 children with acute lymphoblastic leukemia (ALL) and 229 with acute myeloid leukemia (AML), treated on three different Dutch Childhood Oncology Group (DCOG) ALL and three AML protocols. Overall, 23 (2.6%) ALL and 44 (19.2%) AML patients died. Early death (ED, before remission was reached) occurred in nine ALL (1%) and thirty AML (13.1%) patients, including three and ten deaths before treatment was initiated. Chemotherapy-related mortality in remission (CRM) occurred in nine ALL (1.1%) and eight AML (4.4%) patients. For ALL, both ED and CRM declined over time, although this was not statistically significant. For AML a decrease in ED was observed (from 26% to approximately 10%), but counter-balanced by an increase in CRM (from 3 to 8%), maybe related to the scheduling of intensification blocks in AML-92/94. Including transplant-related mortality, death in CR rates in AML increased from 3 to 15% in the last study. The main cause of ED was hemorrhage, often associated with hyperleucocytosis, and infection for CRM. We conclude that mortality dropped favorably in ALL, but not in AML. Especially for AML, effective but less toxic therapy and better supportive care guidelines need to be developed.
我们分析了875例急性淋巴细胞白血病(ALL)患儿和229例急性髓细胞白血病(AML)患儿在三种不同的荷兰儿童肿瘤学组(DCOG)ALL方案和三种AML方案治疗下,因耐药疾病或复发以外的死亡原因。总体而言,23例(2.6%)ALL和44例(19.2%)AML患者死亡。早期死亡(ED,在达到缓解之前)发生在9例ALL(1%)和30例AML(13.1%)患者中,包括在开始治疗前有3例和10例死亡。缓解期化疗相关死亡率(CRM)发生在9例ALL(1.1%)和8例AML(4.4%)患者中。对于ALL,ED和CRM均随时间下降,尽管这在统计学上不显著。对于AML,观察到ED有所下降(从26%降至约10%),但被CRM的增加(从3%增至8%)所抵消,这可能与AML - 92/94强化治疗阶段的安排有关。包括移植相关死亡率在内,AML完全缓解期死亡率在上一项研究中从3%增至15%。ED的主要原因是出血,常与白细胞增多症相关,而CRM的主要原因是感染。我们得出结论,ALL的死亡率呈有利下降,但AML并非如此。特别是对于AML,需要制定有效但毒性较小的治疗方法和更好的支持治疗指南。