Proctor S J, Taylor P R, Stark A, Carey P J, Bown N, Hamilton P J, Reid M M
Department of Haematology, Royal Victoria Infirmary, Newcastle upon Tyne.
Leukemia. 1995 Jul;9(7):1246-51.
The aim of this study was to collect prospectively unselected, population-based data on young adults with acute myeloid leukaemia (AML) over a 9-year period and to evaluate the impact on survival of the introduction of allogeneic transplantation performed in first remission. The population within the Northern Region of England is 3.09 million. During the study period a total of 149 de novo patients between 15 and 55 years old presented. The incidence of AML was 0.79 per 10(5) (age-specific population) in the 15-24-year-old group, 0.85 per 10(5) in the group 25-39 years old and 1.35 per 10(5) in the 40-55-year-old group. Remission induction success varied with age (74% for patients < 40 years and 58% for patients 40-55 years). In the 15-40 year old group 28 patients had an HLA-matched donor, 22 patients had a transplant (one syngeneic) and 24 patients in the 15-40-year-old group in remission at 6 months did not have a transplant. The allogeneic group < 40 years old had an event-free survival (EFS) at 4 years of 62%, whereas patients of the same age who received chemotherapy alone had an EFS at 4 years of 24%. A small heterogeneous group of 14 patients who had intensification with autotransplant are not included in this analysis. The population study approach demonstrates the difficulties of introducing uniform treatment strategy in this disease group. The study confirms the view that allogeneic transplant in first remission in the 15-40-year-old group is the treatment of choice. Unfortunately the overall impact of transplant on the population is not great since only 22 of 149 patients (14%) were able to receive an allograft in first remission.
本研究的目的是前瞻性收集9年间未经选择的、基于人群的年轻急性髓系白血病(AML)患者数据,并评估首次缓解期进行异基因移植对生存率的影响。英格兰北部地区人口为309万。研究期间,共有149例年龄在15至55岁之间的初发患者就诊。15至24岁组AML发病率为每10(5)(特定年龄人群)0.79例,25至39岁组为每10(5)0.85例,40至55岁组为每10(5)1.35例。缓解诱导成功率随年龄而异(<40岁患者为74%,40至55岁患者为58%)。在15至40岁组中,28例患者有HLA匹配供者,22例患者接受了移植(1例同基因移植),15至40岁组中6个月时缓解但未接受移植的患者有24例。<40岁的异基因移植组4年无事件生存率(EFS)为62%,而单纯接受化疗的同年龄患者4年EFS为24%。14例接受自体移植强化治疗的异质性小群体患者未纳入本分析。人群研究方法表明在该疾病组引入统一治疗策略存在困难。该研究证实了15至40岁组首次缓解期进行异基因移植是首选治疗方法的观点。不幸的是,移植对总体人群的影响不大,因为149例患者中只有22例(14%)能够在首次缓解期接受同种异体移植。