Germing U, Kündgen A, Gattermann N
Department of Haematology, Oncology and Clinical Immunology, Heinrich-Heine- University, Düsseldorf, Germany.
Leuk Lymphoma. 2004 Jul;45(7):1311-8. doi: 10.1080/1042819042000207271.
The clinical course of chronic myelomonocytic leukemia (CMML) is extremely variable, and disease progression can occur at any time from diagnosis. Median survival is about 20 months. About 20% of patients develop acute myeloid leukaemia (AML). Multivariate analyses performed by several groups showed that elevated medullary blast count, low haemoglobin, elevated serum lactate dehydrogenase (LDH), and perhaps an increased lymphocyte count, are the most important independent prognostic parameters, whereas karyotype analysis was not consistently shown to yield additional prognostic information. Applying different scoring systems to 288 CMML patients included in the Düsseldorf MDS Registry, we found that the International Prognostic Scoring System (IPSS) was not useful for defining risk groups in CMML, while the Spanish Score, the modified Bournemouth Score, the Düsseldorf Score, and probably the MDAP Score, identified patient groups differing significantly in survival. These scores should therefore be employed for clinical decision making and for risk stratification in the context of clinical trials.
慢性粒单核细胞白血病(CMML)的临床病程变化极大,疾病进展可在诊断后的任何时间发生。中位生存期约为20个月。约20%的患者会发展为急性髓系白血病(AML)。多个研究小组进行的多变量分析表明,骨髓原始细胞计数升高、血红蛋白水平低、血清乳酸脱氢酶(LDH)升高,以及可能的淋巴细胞计数增加,是最重要的独立预后参数,而核型分析并未始终显示能提供额外的预后信息。对杜塞尔多夫骨髓增生异常综合征登记处纳入的288例CMML患者应用不同的评分系统,我们发现国际预后评分系统(IPSS)对CMML风险组的定义并无帮助,而西班牙评分、改良的伯恩茅斯评分、杜塞尔多夫评分以及可能的MDAP评分,可识别出生存率有显著差异的患者组。因此,这些评分应用于临床试验背景下的临床决策和风险分层。