慢性髓性白血病:墨西哥城单一机构的临床流行病学和治疗描述

Alvaro Aguayo , Eunice Garcia-Alvarez , Yael Cazares-Ordonez , Erick Crespo-Solis , Deborah Martinez-Baños , Elizabeth Guadarrama-Beltran , Eduardo E. Cervera-Ceballos , Xavier Lopez-Karpovitch
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引用次数: 25

摘要

背景:慢性髓性白血病(chronic myeloid leukemia, CML)是一种由费城染色体编码蛋白引起的恶性疾病。甲磺酸伊马替尼(Imatinib mesylate, IM)现在是所有阶段CML的治疗选择。发展中国家CML的临床流行病学信息在目前的文献中是分散的。患者和方法我们报告了墨西哥一家机构的一组CML各阶段患者的临床流行病学特征和对IM治疗的反应。此外,我们描述了标准g带细胞遗传学的失败率,并将成功的标准细胞遗传学与荧光原位杂交(FISH)的关联联系起来,以验证我们患者群体的反应结果。评估了99张医疗图表。57例患者接受IM治疗,历史组包括42例患者。结果中位年龄为37岁,im治疗队列的中位随访时间为26.4个月。细胞遗传学与FISH的相关性为0.719 (P = 0.01)。im治疗组的完全细胞遗传学缓解率为88.1%,而历史组为4.8%。先前接受干扰素-α (INF-α)治疗的患者有58.8%的完全细胞遗传学应答,而先前接受干扰素-α治疗的患者有77.8%的完全细胞遗传学应答。结论:我们的报告描述了一组具有社会经济和文化限制的墨西哥CML患者的全面情况。除诊断年龄中位数外,临床流行病学特征和有效率与其他系列一致。荧光原位杂交是监测CML的可靠方法。然而,在标准细胞遗传学检测和聚合酶链反应不太可靠的情况下,FISH在监测CML中的作用需要更彻底地阐明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic Myeloid Leukemia: A Clinicoepidemiologic and Therapeutic Description of a Single Institution in Mexico City

Background

Chronic myeloid leukemia (CML) is a malignant disease caused by the protein coded by the Philadelphia chromosome. Imatinib mesylate (IM) is now the treatment of choice for all stages of CML. Clinicoepidemiologic information on CML from developing countries is scattered in the current literature

Patients and Methods

We report on the clincoepidemiologic features and response to therapy with IM in a cohort of patients with all stages of CML at a Mexican institution. Additionally, we describe the failure rate of standard G-banding cytogenetics, and correlate the association of successful standard cytogenetics with fluorescence in situ hybridization (FISH) to validate the results of responses in our patient population. Ninety-nine medical charts were evaluated. Fifty-seven patients were treated with IM, and a historical group consisted of 42 patients.

Results

The median age was 37 years, and the median follow-up of the IM-treated cohort was 26.4 months. The correlation between cytogenetics and FISH was 0.719 (P = .01). The complete cytogenetic response was 88.1% in the IM-treated group, versus 4.8% in the historical group. Patients previously treated with interferon-α (INF-α) had a complete cytogenetic response of 58.8%, versus 77.8% of patients previously treated who were naive to INF-α.

Conclusion

Our report describes a comprehensive picture of a group of patients with CML representative of the Mexican population with socioeconomic and cultural constraints. Except for median age at diagnosis, clinicoepidemiologic features and response rates are in accordance with other series. Fluorescence in situ hybridization was a reliable method for monitoring CML at our institution. However, the role of FISH in monitoring CML, where standard cytogenetic testing and the polymerase chain reaction are less reliable, needs to be clarified more thoroughly.

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