Lu Ping-Fan, Deng Li-Nan, Meng Fan-Kai, Wang Ying, Xiao Min, Li Deng-Ju
Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Curr Med Sci. 2022 Feb;42(1):77-84. doi: 10.1007/s11596-022-2533-4. Epub 2022 Jan 28.
Although the effect of decitabine on myelodysplastic syndrome (MDS) has been demonstrated, merely a proportion of patients respond to therapy, and no well-recognized predictors have been identified. This study was conducted to investigate the effectiveness of decitabine in real-world clinical practice, and determine the predictive factors of response and overall survival (OS) in MDS patients.
Clinical and pathological data were collected from 94 patients and analyzed. These patients were reclassified according to the 2016 World Health Organization classification criteria, and restratified by International Prognostic Scoring System prognostic scores. The response evaluation was performed according to the 2006 modified International Working Group response criteria.
In this study, 62% of patients responded to decitabine. Among these patients, 15 patients (16%) obtained complete remission (CR), 15 patients (16%) obtained marrow CR with hematologic improvement (HI), 20 patients (21%) obtained marrow CR without HI, and 8 patients (9%) only obtained HI, and no patient botained partial remission. The OS of the responders was significantly longer than that of non-responders (67 months vs. 7 months, P<0.001). The OS in patients with and without platelet doubling was significantly different in both the low/intermediate and high/very high risk groups (P=0.0398 and P=0.0330). The multivariate analysis revealed that platelet doubling after the first decitabine cycle is an independent predictor of response and OS in MDS patients (P=0.002 and P=0.008).
Decitabine is effective for treating MDS patients in real-world clinical practice. Furthermore, platelet doubling after the first decitabine cycle can be used as a predictor of response and survival in MDS patients.
虽然地西他滨对骨髓增生异常综合征(MDS)的疗效已得到证实,但仅有一部分患者对治疗有反应,且尚未发现得到广泛认可的预测指标。本研究旨在调查地西他滨在实际临床实践中的有效性,并确定MDS患者反应及总生存期(OS)的预测因素。
收集94例患者的临床和病理数据并进行分析。这些患者根据2016年世界卫生组织分类标准重新分类,并根据国际预后评分系统预后分数重新分层。根据2006年修订的国际工作组反应标准进行反应评估。
本研究中,62%的患者对地西他滨有反应。在这些患者中,15例(16%)获得完全缓解(CR),15例(16%)获得伴有血液学改善(HI)的骨髓CR,20例(21%)获得无HI的骨髓CR,8例(9%)仅获得HI,且无患者获得部分缓解。有反应者的OS显著长于无反应者(67个月对7个月,P<0.001)。在低/中危组和高/极高危组中,血小板计数翻倍和未翻倍的患者的OS均有显著差异(P=0.0398和P=0.0330)。多变量分析显示,首个地西他滨周期后血小板计数翻倍是MDS患者反应和OS的独立预测指标(P=0.002和P=0.008)。
地西他滨在实际临床实践中对治疗MDS患者有效。此外,首个地西他滨周期后血小板计数翻倍可作为MDS患者反应和生存的预测指标。