Chronic Myeloid Leukemia in Adolescents and Young Adults: Clinicopathological Variables and Outcomes.

IF 2.5 3区 医学 Q3 ONCOLOGY Oncology Pub Date : 2024-07-16 DOI:10.1159/000539982
Mohammad A J Abdulla, Mahmood B Aldapt, Prem Chandra, Susanna El Akiki, Awni Alshurafa, Abdulqadir J Nashwan, Liam J Fernyhough, Sundus Sardar, Ammar Chapra, Mohamed A Yassin
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Abstract

Introduction: Adolescents and young adults (AYAs) diagnosed with chronic myeloid leukemia (CML) constitute a significant demographic group, particularly in regions with youthful populations like Qatar. Despite the global median age of CML diagnosis being 65 years, Qatar's age distribution reflects a younger cohort. This study investigates whether AYAs with CML exhibit distinct clinicopathological characteristics or outcomes compared to older age groups.

Methods: A total of 224 CML patients were enrolled, including 114 AYAs (defined as ages 15 through 39). Demographic and clinical parameters, including gender, BMI, BCR-ABL1 transcript type, white blood cell (WBC) count, hemoglobin level, platelet count, and spleen size, were compared between AYAs and older patients. Prognostic scoring systems (Sokal, Hasford, EUTOS, and ELTS) and molecular response rates (MMR and DMR) were also evaluated.

Results: AYAs demonstrated higher WBC counts at diagnosis (median 142.3 vs. 120; p = 0.037) and lower hemoglobin levels (10.5 vs. 11.40; p = 0.004) compared to older patients. Spleen size was significantly larger in AYAs (18.8 vs. 15.5; p = 0.001). While AYAs showed better prognostic scores by Sokal and Hasford criteria, EUTOS and ELTS scores indicated comparable risk stratification. However, AYAs exhibited lower rates of MMR (56.7 vs. 73.4%; p = 0.016) and achieved MMR at a slower pace (median time 130 vs. 103 months; p = 0.064). Similarly, the percentage of DMR was lower in AYAs (37.1 vs. 46.8%; p = 0.175).

Conclusion: Despite their younger age, AYAs with CML displayed poorer prognoses compared to older patients. These findings underscore the importance of tailored management strategies for AYAs with CML to optimize outcomes in this distinct patient population.

Key point: AYAs are underrepresented in CML studies and risk scores, so this is the focus of this study.

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青少年慢性粒细胞白血病:临床病理变量和结果
导言:被诊断为慢性髓性白血病(CML)的青少年和年轻成人(AYAs)是一个重要的人口群体,尤其是在卡塔尔这样人口年轻化的地区。尽管全球确诊 CML 的中位年龄为 65 岁,但卡塔尔的年龄分布却反映了一个更年轻的群体。本研究探讨了与年龄较大的群体相比,患有 CML 的青壮年患者是否表现出不同的临床病理特征或结果:共纳入 224 名 CML 患者,其中包括 114 名 AYAs(定义为 15 至 39 岁)。比较了AYAs和老年患者的人口统计学和临床参数,包括性别、体重指数、BCR-ABL1转录本类型、白细胞(WBC)计数、血红蛋白水平、血小板计数和脾脏大小。此外,还对预后评分系统(Sokal、Hasford、EUTOS 和 ELTS)和分子反应率(MMR 和 DMR)进行了评估:与老年患者相比,青壮年患者诊断时的白细胞计数更高(中位数为 142.3 vs. 120;p = 0.037),血红蛋白水平更低(10.5 vs. 11.40;p = 0.004)。青少年患者的脾脏体积明显更大(18.8 vs. 15.5; p = 0.001)。根据 Sokal 和 Hasford 标准,AYAs 的预后评分较高,而 EUTOS 和 ELTS 评分显示的风险分层效果相当。然而,AYAs 的 MMR 率较低(56.7% 对 73.4%;P = 0.016),且 MMR 的实现速度较慢(中位时间 130 个月对 103 个月;P = 0.064)。同样,AYAs 的 DMR 百分比也较低(37.1% vs. 46.8%;p = 0.175):结论:尽管青壮年 CML 患者年龄较小,但与老年患者相比,他们的预后较差。这些发现强调了为患有 CML 的青少年量身定制管理策略以优化这一特殊患者群体预后的重要性。
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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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