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年轻个体的骨髓纤维化伴髓外化生:疾病特征、预后因素及风险组的识别

Myelofibrosis with myeloid metaplasia in young individuals: disease characteristics, prognostic factors and identification of risk groups.

作者信息

Cervantes F, Barosi G, Demory J L, Reilly J, Guarnone R, Dupriez B, Pereira A, Montserrat E

机构信息

Haematology Department, Hospital Clínic, IDIBAPS, Barcelona, Spain.

出版信息

Br J Haematol. 1998 Aug;102(3):684-90. doi: 10.1046/j.1365-2141.1998.00833.x.

DOI:10.1046/j.1365-2141.1998.00833.x
PMID:9722294
Abstract

Myelofibrosis with myeloid metaplasia (MMM) is an uncommon disorder in young individuals, for whom haemopoietic stem cell transplantation offers the only possibility of cure. However, although the latter procedure is associated with significant morbidity and mortality, the clinical course of MMM is variable, with some patients surviving for less than a year and others showing an indolent course. Selection of young MMM patients for transplantation or other newer therapies is currently difficult since no prognostic data exists for this subgroup. In the present collaborative study a number of initial clinical and laboratory parameters have been evaluated for prognosis in 121 MMM patients aged 55 years or less. Median survival of the series was 128 months (95% CI 90-172). In the Cox proportional hazard regression model three initial variables were independently associated with shorter survival: Hb <10 g/dl (P <0.0001), the presence of constitutional symptoms (fever, sweats, weight loss) (P=0.001), and circulating blasts >/=1% (P=0.003). Based on the above three criteria, of the 116 patients with complete data, two groups were identified: a 'low-risk' group, characterized by 88 patients with up to one adverse prognostic factor, in whom MMM had an indolent course (median survival 176 months, 95% CI 130-188), and a 'high-risk' group, including 28 patients with two or three factors, who had a more aggressive disease (median survival 33 months, 95% CI 20-42). The above prognostic scoring system showed a high positive predictive value, sensitivity and specificity to predict survival in the series, and could be of help in making treatment decisions in young patients with MMM.

摘要

骨髓纤维化伴髓外化生(MMM)在年轻人中是一种罕见疾病,造血干细胞移植是唯一能治愈该病的方法。然而,尽管该手术伴有显著的发病率和死亡率,但MMM的临床病程多变,有些患者存活时间不到一年,而另一些患者病程进展缓慢。目前,由于缺乏该亚组患者的预后数据,很难选择年轻的MMM患者进行移植或其他新疗法。在本协作研究中,对121例55岁及以下的MMM患者的一些初始临床和实验室参数进行了预后评估。该系列患者的中位生存期为128个月(95%可信区间90 - 172)。在Cox比例风险回归模型中,三个初始变量与较短生存期独立相关:血红蛋白<10 g/dl(P <0.0001)、存在全身症状(发热、盗汗、体重减轻)(P = 0.001)以及循环原始细胞≥1%(P = 0.003)。根据上述三个标准,在116例有完整数据的患者中,分为两组:“低风险”组,其特征为88例患者最多有一个不良预后因素,MMM病程进展缓慢(中位生存期176个月,95%可信区间130 - 188);“高风险”组,包括28例有两个或三个因素的患者,疾病进展更为迅速(中位生存期33个月,95%可信区间20 - 42)。上述预后评分系统对该系列患者生存期的预测具有较高的阳性预测值、敏感性和特异性,有助于指导年轻MMM患者的治疗决策。

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