Chen Yue-dan, Xu Ze-feng, Cui Rui, Wang Jie-yu, Zhang Tian-jiao, Fang Li-wei, Zhang Hong-li, Qin Tie-jun, Zhang Yue, Xiao Zhi-jian
Institute of Hematology and Blood Diseases Hospital, CAMS & PUMC, State Key Laboratory of Experimental Hematology, Tianjin 300020, China.
Zhonghua Xue Ye Xue Za Zhi. 2012 Jul;33(7):532-5.
To investigate the prognostic value of thrombocytopenia in patients with primary myelodysplastic syndromes (MDS).
Four hundred and nineteen primary MDS patients were retrospectively analyzed. Kaplan-Meier method, Log-rank test and COX regression model were used to evaluate factors that influence the prognosis.
Two hundred and fifty-six cases (61.1%) had thrombocytopenia (PLT < 100×10(9)/L), one hundred and three cases (24.6%) had severe thrombocytopenia (PLT < 30×10(9)/L). Overall survival (OS) tended to shorten along with the decreasing of platelet count. Univariate analysis indicated that PL < 30×10(9)/L, MCV ≤ 95 fl, LDH ≥ 300 U/L, lymphocyte-like micromegakaryocyte, nucleated RBC PAS positive, IPSS cytogenetic intermediate- and poor-risk were all related with poor prognosis. Moreover, the prognosis of patients with RCMD, RAEB-Ior RAEB-IIwas poorer than that of the other subgroups. Among these parameters, PLT < 30×10(9)/L, MCV ≤ 95 fl, IPSS cytogenetic intermediate- and poor-risk group and RCMD, RAEB-I and RAEB-II had independent prognostic significance in multivariate analysis. Modified WPSS prognostic model was proposed by adopting PLT, MCV, chromosomal karyotype and WHO classification. The OS of patients with low risk, intermediate-1 risk, intermediate-2 risk and high risk were 59, 28, 14 and 4 months, respectively, and there was a statistically significant difference between the groups (P < 0.05).
Severe thrombocytopenia indicated unfavorable prognosis, in combination with MCV, chromosomal karyotype and WHO classification, a modified WPSS prognostic model was proposed and worked well for prognostic indication in patients with MDS.
探讨血小板减少在原发性骨髓增生异常综合征(MDS)患者中的预后价值。
对419例原发性MDS患者进行回顾性分析。采用Kaplan-Meier法、Log-rank检验和COX回归模型评估影响预后的因素。
256例(61.1%)有血小板减少(血小板计数<100×10⁹/L),103例(24.6%)有严重血小板减少(血小板计数<30×10⁹/L)。总生存期(OS)随血小板计数降低而缩短。单因素分析表明,血小板计数<30×10⁹/L、平均红细胞体积(MCV)≤95fl、乳酸脱氢酶(LDH)≥300U/L、淋巴细胞样小巨核细胞、有核红细胞过碘酸雪夫(PAS)阳性、国际预后评分系统(IPSS)细胞遗传学中危和高危均与预后不良相关。此外,难治性血细胞减少伴多系发育异常(RCMD)、难治性贫血伴原始细胞增多-1型(RAEB-Ⅰ)或难治性贫血伴原始细胞增多-2型(RAEB-Ⅱ)患者的预后较其他亚组差。在这些参数中,血小板计数<30×10⁹/L、MCV≤95fl、IPSS细胞遗传学中危和高危组以及RCMD、RAEB-Ⅰ和RAEB-Ⅱ在多因素分析中有独立的预后意义。采用血小板计数、MCV、染色体核型和世界卫生组织(WHO)分类法提出了改良的世界卫生组织预后评分系统(WPSS)预后模型。低危、中危-1、中危-2和高危患者的OS分别为59、28、14和4个月,组间差异有统计学意义(P<0.05)。
严重血小板减少提示预后不良,结合MCV、染色体核型和WHO分类法,提出了改良的WPSS预后模型,该模型在MDS患者的预后评估中效果良好。