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急性早幼粒细胞白血病的长期疗效观察:340 例单中心经验。

Long-term survey of outcome in acute promyelocytic leukemia: a single center experience in 340 patients.

机构信息

The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, People's Republic of China.

出版信息

Med Oncol. 2011 Dec;28 Suppl 1:S513-21. doi: 10.1007/s12032-010-9733-7. Epub 2010 Nov 11.

Abstract

The aims of this study are to investigate the outcome and prognostic factors influencing long-term survival on patients with acute promyelocytic leukemia (APL). A total of 340 APL patients admitted to the Department of Hematology from January 1988 to December 2009 were enrolled in this study. All patients received all-trans retinoic acid (ATRA) and/or arsenic trioxide (ATO) with anthracycline-based induction therapy. After three courses of consolidation chemotherapy, 279 patients received 2 years of maintenance therapy. Survival analyses were carried out using the Kaplan-Meier method and the Cox regression model. In total, 288 achieved CR with the CR rate of 84.7%, and 50 patients died during induction therapy. Univariate analysis identified the following three risk factors for hemorrhagic mortality: fibrinogen level (<1.0 g/l) (P = 0.0007), initial peripheral WBC count(>4 × 10(9)/l) (P = 0.0001), as well as the presence of coagulopathy(P < 0.0001). With a median follow-up of 49 (6-255) months, the estimated 5-year overall survival (OS) and relapse-free survival (RFS) were (89.0 ± 2.4)% and (83.7 ± 2.6)%, respectively. Cox regression analysis of the 290 patients showed initial WBC count, years of diagnosis, and the status of PML-RARα in remission seemed to be independent prognostic indicators for OS and RFS (P = 0.03, P < 0.01 and P = 0.0001, respectively). Cytogenetics in addition to above three variables remained significant for RFS (P = 0.01). Our retrospective observations suggest that the combination of ATRA and/or ATO with anthracycline-based therapy may have useful implications in the perspective of long-term prognosis for adult APL.

摘要

本研究旨在探讨影响急性早幼粒细胞白血病(APL)患者长期生存的预后因素和结局。共纳入 1988 年 1 月至 2009 年 12 月在血液科接受治疗的 340 例 APL 患者。所有患者均接受全反式维甲酸(ATRA)和/或三氧化二砷(ATO)联合蒽环类药物诱导治疗。三疗程巩固化疗后,279 例患者接受 2 年维持治疗。采用 Kaplan-Meier 法和 Cox 回归模型进行生存分析。共有 288 例患者达到完全缓解(CR),CR 率为 84.7%,50 例患者在诱导治疗期间死亡。单因素分析发现,出血性死亡率的 3 个危险因素分别为纤维蛋白原水平(<1.0 g/L)(P = 0.0007)、初始外周白细胞计数(>4×10(9)/l)(P = 0.0001)和凝血功能障碍(P < 0.0001)。中位随访 49(6-255)个月后,估计 5 年总生存(OS)和无复发生存(RFS)分别为(89.0 ± 2.4)%和(83.7 ± 2.6)%。对 290 例患者进行 Cox 回归分析,结果显示,初诊白细胞计数、诊断年限和缓解时 PML-RARα 状态似乎是 OS 和 RFS 的独立预后指标(P = 0.03、P < 0.01 和 P = 0.0001)。除上述 3 个变量外,细胞遗传学对 RFS 也有显著影响(P = 0.01)。本回顾性观察提示,ATRA 和/或 ATO 联合蒽环类药物治疗可能对成人 APL 的长期预后具有重要意义。

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