Park Min Jae, Kim Hee-Jin, Kim Sun-Hee, Kim Dong Hwan, Kim Seok Jin, Jang Jun Ho, Kim Kihyun, Kim Won Seog, Jung Chul Won
Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Eur J Haematol. 2008 Nov;81(5):364-73. doi: 10.1111/j.1600-0609.2008.01124.x. Epub 2008 Jul 10.
This study was undertaken to evaluate the prognostic value of the WHO Classification-Based Prognostic Scoring System (WPSS) and to compare it with that of the International Prognostic Scoring System (IPSS).
149 patients de novo diagnosed as having myelodysplastic syndrome between December 1994 and February 2007, were evaluated retrospectively.
WPSS presented an excellent method for risk-stratifying patients into five subgroups, with different risks of death and leukaemic evolution. On univariate analysis, three components of WPSS - cytogenetic risk, WHO category and transfusion dependency - had good correlations with overall survival (OS) and time to leukaemic evolution (TTL). However, one component of IPSS - number of peripheral cytopenias - did not correlate with OS or TTL. WPSS could distinguish the truly low-risk patients (very low) who had an excellent long-term survival with rare leukaemic evolution, while IPSS could not. These patients should be managed with clinical observation and delayed treatment strategies. Furthermore, on multivariate analysis for OS, WPSS was found to be an independent prognostic factor for survival along with age [P = 0.04; hazard ratio (HR) = 1.71; 95% confidence interval (CI) 1.02-2.85] and lactate dehydrogenase (LDH) (P = 0.002; HR = 2.47; 95% CI 1.41-4.31). On the other hand, the prognostic significance of IPSS was not confirmed.
These results suggest that the WPSS might be a more powerful predictor of prognosis than IPSS and that independent validation of several other, larger data sets should be necessary.
本研究旨在评估基于世界卫生组织(WHO)分类的预后评分系统(WPSS)的预后价值,并将其与国际预后评分系统(IPSS)进行比较。
回顾性评估了1994年12月至2007年2月期间初诊为骨髓增生异常综合征的149例患者。
WPSS是一种将患者分为五个亚组的优秀风险分层方法,各亚组具有不同的死亡风险和白血病进展风险。单因素分析显示,WPSS的三个组成部分——细胞遗传学风险、WHO类别和输血依赖——与总生存期(OS)和白血病进展时间(TTL)具有良好的相关性。然而,IPSS的一个组成部分——外周血细胞减少数量——与OS或TTL无关。WPSS能够区分真正的低风险患者(极低风险),这些患者长期生存率极佳,白血病进展罕见,而IPSS则无法做到。这些患者应采用临床观察和延迟治疗策略进行管理。此外,在OS的多因素分析中,发现WPSS与年龄[P = 0.04;风险比(HR)= 1.71;95%置信区间(CI)1.02 - 2.85]和乳酸脱氢酶(LDH)(P = 0.002;HR = 2.47;95% CI 1.41 - 4.31)一样,是生存的独立预后因素。另一方面,IPSS的预后意义未得到证实。
这些结果表明,WPSS可能比IPSS更能有力地预测预后,并且有必要对其他几个更大的数据集进行独立验证。