Rodrigues C A, Chauffaille M L L F, Pelloso L A F, Ghaname F S, Kerbauy D M B, Campos M G V, Yamamoto M
Disciplina de Hematologia e Hemoterapia, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, Brasil.
Braz J Med Biol Res. 2003 Jun;36(6):703-8. doi: 10.1590/s0100-879x2003000600004. Epub 2003 Jun 3.
Acute myeloid leukemia (AML) is a disease predominantly of older adults. Treatment of AML in the elderly is complicated not only by comorbidities but also by the high prevalence of poor prognosis markers. Thirty-one consecutive unselected patients with AML older than 60 years (representing 33% of all AML cases diagnosed at our institution during the same period) were followed over a period of 5 years (1997-2002). A high incidence of AML with multilineage dysplasia (45%) and no favorable cytogenetic abnormalities but 62% intermediate and 38% unfavorable karyotypes were found. Sixteen patients (52%) were selected for induction of intensive cytotoxic treatment and complete remission was achieved only by some of these intensively treated patients (7 of 16). Of these, 3 remained alive without disease (median: 11 months), 1 patient died shortly after complete remission, and 3 patients relapsed and died from refractory disease. Only 1 patient that was refractory to intensive cytotoxic treatment remained alive with disease under supportive care. Fifteen patients (48%) were managed with palliative/supportive care: 7 received palliative treatment and supportive care, 8 received supportive care only, and 4 patients remained alive with disease under supportive care (median: 9 months). Mortality rate was 74% and overall survival at two years was 12%. To the best of our knowledge, there is no previous report regarding elderly patients with AML in Brazilian subsets. The present data are similar to previously reported studies showing that elderly AML patients are not only older but also biologically distinct from younger AML patients, particularly in terms of the high incidence of poor prognostic karyotypes and resistance to therapy.
急性髓系白血病(AML)主要是一种老年疾病。老年AML患者的治疗不仅因合并症而复杂,还因预后不良标志物的高患病率而复杂。对31例连续入选的60岁以上AML患者(占同期在我院诊断的所有AML病例的33%)进行了为期5年(1997 - 2002年)的随访。发现多系发育异常的AML发生率较高(45%),且无有利的细胞遗传学异常,但有62%的中间核型和38%的不良核型。16例患者(52%)被选入强化细胞毒性治疗诱导组,其中只有部分接受强化治疗的患者(16例中的7例)实现了完全缓解。其中,3例无病存活(中位数:11个月),1例在完全缓解后不久死亡,3例复发并死于难治性疾病。只有1例对强化细胞毒性治疗难治的患者在支持治疗下带疾病存活。15例患者(48%)接受姑息/支持治疗:7例接受姑息治疗和支持治疗,8例仅接受支持治疗,4例患者在支持治疗下带疾病存活(中位数:9个月)。死亡率为74%,两年总生存率为12%。据我们所知,之前没有关于巴西亚组老年AML患者的报告。目前的数据与之前报道的研究相似,表明老年AML患者不仅年龄更大,而且在生物学上与年轻AML患者不同,特别是在不良预后核型的高发生率和对治疗的耐药性方面。