Neto Miguel Pedro de Queiroz, da Costa Larissa, Lisboa Erica Sabrine Angelo, Silva Silvia Nathalia Bueno, de Azambuja Ana Paula, Nunes Elenaide Coutinho, Bendlin Rodrigo Miguel
Hospital de Clínicas da Universidade Federal do Paraná (HC-UFPR), Curitiba, PR, Brazil.
Hospital de Clínicas da Universidade Federal do Paraná (HC-UFPR), Curitiba, PR, Brazil.
Hematol Transfus Cell Ther. 2023 Jul;45 Suppl 2(Suppl 2):S18-S24. doi: 10.1016/j.htct.2021.08.016. Epub 2021 Dec 9.
Improving survival of Acute Lymphoblastic Leukemia (ALL) in adult patients has been a challenge. Despite intensive chemotherapy treatment, overall survival is poor. However, several studies demonstrate that young adult patients have better survival when treated with pediatric-based intensive regimens. Considering these results, We decided to treat newly diagnosed ALL patients according to age and risk factors. The goal of this study was to describe the results of this intensive chemotherapy treatment approach for ALL adult patients diagnosed at our institution.
Fifty-eight ALL patients, diagnosed from 2004 to 2013, were included in the analysis. Patients were assigned to either the St. Jude Total Therapy XIIIB high-risk arm (St Jude) or the CALGB 8811 (CALGB). The Kaplan-Meier survival curve was used for the survival analyses and the Cox proportional hazard regression, for multivariable analysis.
The overall survival was 22.9% at 10 years. The St. Jude improved survival, compared to the CALGB (p = 0.007), with 32.6% vs. 7.4% survival rate at 10 years. However, no survival benefit was found for patients younger than 20 years old (p = 0.32). The multivariable analysis demonstrated that undetectable minimal residual disease (MRD) and hematopoietic stem cell transplantation (HSCT) had beneficial impact on survival (p = 0.0007 and p = 0.004, respectively).
ALL is a disease of poor prognosis for adults. The joint effort to standardize treatment and seek solutions is the way to start improving this scenario.
提高成年急性淋巴细胞白血病(ALL)患者的生存率一直是一项挑战。尽管进行了强化化疗,但总体生存率仍很低。然而,多项研究表明,采用基于儿科的强化方案治疗时,年轻成年患者的生存率更高。考虑到这些结果,我们决定根据年龄和风险因素对新诊断的ALL患者进行治疗。本研究的目的是描述在我们机构诊断的成年ALL患者采用这种强化化疗治疗方法的结果。
纳入分析的是2004年至2013年诊断的58例ALL患者。患者被分配到圣裘德全面治疗XIIIB高危组(圣裘德组)或癌症与白血病B组协作组8811(CALGB组)。采用Kaplan-Meier生存曲线进行生存分析,并采用Cox比例风险回归进行多变量分析。
10年总生存率为22.9%。与CALGB组相比,圣裘德组生存率有所提高(p = 0.007),10年生存率分别为32.6%和7.4%。然而,未发现20岁以下患者有生存获益(p = 0.32)。多变量分析表明,不可检测的微小残留病(MRD)和造血干细胞移植(HSCT)对生存有有益影响(分别为p = 0.0007和p = 0.004)。
ALL是一种成年患者预后较差的疾病。共同努力规范治疗并寻求解决方案是开始改善这种情况的途径。