Factors Affecting Early Death and Survival of Patients With Acute Promyelocytic Leukemia Treated With ATRA-Based Therapy Regimens

In a retrospective analysis of data of 288 adult acute promyelocytic leukemia patients, we found an early death rate of 5.9% and overall survival rate of 91.7%. Older age was the only independent risk factor for early death. High white blood cell count and CD15 negativity were risk factors for relap...

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Veröffentlicht in:Clinical lymphoma, myeloma and leukemia myeloma and leukemia, 2019-01, Vol.19 (1), p.e63-e70
Hauptverfasser: Sun, Jianai, Zhu, Jingjing, Zhou, De, Zhu, Lixia, Yang, Xiudi, Xie, Mixue, Li, Li, Huang, Xianbo, Zhu, Mingyu, Zheng, Yanlong, Xie, Wanzhuo, Ye, Xiujin
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Sprache:eng
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Zusammenfassung:In a retrospective analysis of data of 288 adult acute promyelocytic leukemia patients, we found an early death rate of 5.9% and overall survival rate of 91.7%. Older age was the only independent risk factor for early death. High white blood cell count and CD15 negativity were risk factors for relapse, and FLT3 mutation and older age were factors for poorer prognosis. To perform a retrospective analysis of the prognostic relevance of clinicopathologic parameters in a well-documented cohort of patients treated with all-trans-retinoic acid (ATRA)-based induction regimens in order to discover which indicators can predict a high risk of early death (ED) and patient survival. We analyzed data of 288 newly diagnosed adult acute promyelocytic leukemia patients in Hangzhou, China. The median follow-up time was 32 months (range, 6-78 months). The 3-year disease-free and overall survival rates were 90.83% and 91.69%, respectively. In the multivariable analysis, older age (≥ 60 years) was the only independent risk factor for ED (hazard ratio [HR] = 15.057; P = .004). High white blood cell count was not a risk factor for ED (P = .055), but it was for relapse (HR = 2.7; P = .009). FLT3 mutation (HR = 3.9; 95% confidence interval, 1.4 to 10; P = .007) and older age (≥ 60 years) (HR = 5.3; 95% confidence interval, 2.4 to 11; P < .001) were prognostic factors for poorer disease-free and overall survival. Interestingly, CD15 negativity (HR = 0.23; P = .049) was a prognostic factor for relapse. The ED rate was 5.9% (17/288 patients). The perceived impact of the identification of these high-risk factors should be described in order to decide whether any modifications to treatment strategy should be entertained.
ISSN:2152-2650
2152-2669
DOI:10.1016/j.clml.2018.08.001