Clinical and Prognostic Analysis of Adult Acute Lymphoblastic Leukemia

Bao‐an Chen, Zheng Shi
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Abstract

Objective: To analyse clinical characteristics of adult patients with acute lymphoblastic leukemia (ALL) and explore prognostic factors to provide evidence for the stratification of prognostic risk and the formulation of individualized therapy. Methods: A total of 65 adult patients with newly diagnosed ALL were reviewed. Their clinical data were collected, and their overall survival was followed up. We compared the effects of different clinical features on therapeutic efficacy and long-term prognosis. Data analysis was conducted by SPSS 25.0 statistical software. P < 0.05 was considered statistically significant. Results: A total of 65 adult patients with newly diagnosed ALL, including 31 males and 34 females, were enrolled in this study, with a median onset age of 48 (range, 18-85) years. After 1 course of induction therapy, bone marrow puncture was performed to evaluate, and further demonstrate that 49 patients achieved complete response (CR), with a total CR rate (CRR) of 75.4%. Among 65 patients, the median overall survival was 15.5 (range,1.0-100.0) months, and the median disease-free survival was 9.0 (range, 0.0-99.0) months. Survival analysis showed that worse long-term outcome was associated with age (≥60 years), haemoglobin (Hb<60g/L), platelet (PLT<30×109/L), lactic dehydrogenase (LDH≥400U/L) at initial diagnosis, CD10 negative, and failure to reach CR within 4 weeks after induction therapy, whereas timely hematopoietic stem cell transplantation (HSCT) significantly improved the survival of patients. Univariate analysis suggested that age at onset, the initial level of low PLT and high LDH, and HSCT were risk factors for 2-year OS and 2-year DFS of adult ALL patients. Moreover, multivariate analysis showed that initial PLT level was an independent risk factor for the prognosis of adult ALL patients, and CR within 4 weeks after induction and HSCT could improve patients’ overall survival. Conclusion: Long-term outcome for adult ALL patients is poor. Clinical characteristics, including elder age, severe anemia, low PLT level, high LDH level, CD10 negative and so on, make poor clinical induction effect on such patients. However, achieving CR within 4 weeks and actively accepting HSCT can significantly improve the prognosis of adult ALL.
成人急性淋巴细胞白血病的临床与预后分析
目的:分析成年急性淋巴细胞白血病(ALL)患者的临床特点,探讨影响预后的因素,为预后风险分层及制定个体化治疗方案提供依据。方法:对65例新诊断ALL的成人患者进行回顾性分析。收集他们的临床资料,并对他们的总体生存进行随访。比较不同临床特征对治疗效果及远期预后的影响。采用SPSS 25.0统计软件进行数据分析。P < 0.05为差异有统计学意义。结果:本研究共纳入65例新诊断ALL的成年患者,其中男性31例,女性34例,中位发病年龄48岁(范围18-85岁)。诱导治疗1个疗程后行骨髓穿刺评价,进一步证实49例患者达到完全缓解(CR),总CR率(CRR)为75.4%。65例患者中位总生存期为15.5个月(范围1.0-100.0),中位无病生存期为9.0个月(范围0.0-99.0)。生存分析显示,较差的长期预后与年龄(≥60岁)、初诊时血红蛋白(Hb<60g/L)、血小板(PLT<30×109/L)、乳酸脱氢酶(LDH≥400U/L)、CD10阴性、诱导治疗后4周内未能达到CR相关,而及时的造血干细胞移植(HSCT)可显著改善患者的生存。单因素分析提示,发病年龄、初始低PLT和高LDH水平、HSCT是成人ALL患者2年OS和2年DFS的危险因素。此外,多因素分析显示,初始PLT水平是成人ALL患者预后的独立危险因素,诱导和移植后4周内的CR可提高患者的总生存率。结论:成人ALL患者的长期预后较差。高龄、重度贫血、PLT水平低、LDH水平高、CD10阴性等临床特点使得该类患者的临床诱导效果较差。然而,在4周内达到CR并积极接受造血干细胞移植可显著改善成人ALL的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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