Hematology and Immunology Institute, Havana, Cuba.
MEDICC Rev. 2011 Jan;13(1):35-40. doi: 10.37757/MR2011V13.N1.9.
Chronic myeloid leukemia is the first malignant disease to be associated with a genetic lesion and is the first leukemia to provide a genotype model conducive to targeted molecular therapy. It is a chronic clonal myeloproliferative disorder, originating in a pluripotent stem cell common to all three hematopoietic lineages, characterized by overproduction of myeloid cells in all stages of maturation. Approval of the use of imatinib in the United States in 2001 and its introduction in the treatment of chronic myeloid leukemia changed the evolution and prognosis of the disease and began the era of molecular therapy for malignancies. Imatinib is highly effective and causes fewer adverse reactions than earlier treatments based on interferon and hydroxyurea. In Cuba, chronic myeloid leukemia has been treated with interferon since 1998. Starting in 2003, imatinib was gradually introduced for use in newly-diagnosed chronic myeloid leukemia patients.
Evaluate the use of imatinib as first-line therapy for chronic myeloid leukemia in a group of Cuban patients, based on hematologic, cytogenetic, and molecular response; overall and event-free survival rates; and most frequency and severity of adverse reactions.
During May 2003 to May 2008, 33 newly-diagnosed chronic myeloid leukemia patients (25 adults, 8 children; <6 months from diagnosis) received a single daily oral dose of imatinib 400 mg from the time of study enrollment. Variables used: (1) to evaluate treatment efficacy: hematologic, cytogenetic, and molecular response; overall and event-free survival; and (2) to evaluate safety: presence of adverse reactions leading to definitive interruption of treatment or death.
Complete hematologic response occurred in 100% of patients, major cytogenetic response in 90.9%, and complete cytogenetic response in 48.5%. Molecular response occurred in 36.4% of patients. With a mean follow-up of 39 months, overall survival was 96% and estimated five-year event-free survival was 85%. No adverse reactions occurred in 39.5% of patients. Adverse reactions most frequently observed were myelosuppression (24.2%) and digestive disorders (21.2%). These were followed, in decreasing order, by edema, primarily orbital (9.1%), skin depigmentation (3%), and cardiac arrhythmias (3%).
In the present study, imatinib was effective first-line therapy for patients with newly-diagnosed chronic myeloid leukemia, as determined by overall and event-free survival rates. No severe adverse reactions were observed.
慢性髓性白血病是第一个与遗传病变相关的恶性疾病,也是第一个提供有利于靶向分子治疗的基因型模型的白血病。它是一种慢性克隆性髓系增殖性疾病,起源于所有三种造血谱系共有的多能干细胞,其特征是所有成熟阶段的髓系细胞过度生成。2001 年,美国批准伊马替尼用于治疗,并将其引入慢性髓性白血病的治疗中,这改变了疾病的演变和预后,并开启了恶性肿瘤分子治疗的时代。伊马替尼的疗效很高,且不良反应比基于干扰素和羟基脲的早期治疗少。在古巴,自 1998 年以来,慢性髓性白血病一直使用干扰素进行治疗。从 2003 年开始,逐渐引入伊马替尼用于新诊断的慢性髓性白血病患者。
根据血液学、细胞遗传学和分子反应、总生存率和无事件生存率以及最常见和最严重的不良反应发生率,评估一组古巴患者使用伊马替尼作为慢性髓性白血病一线治疗的效果。
在 2003 年 5 月至 2008 年 5 月期间,33 名新诊断的慢性髓性白血病患者(25 名成人,8 名儿童;诊断后<6 个月)在研究入组时接受了每日一次口服 400mg 伊马替尼的单一治疗。使用的变量有:(1)评估治疗效果:血液学、细胞遗传学和分子反应、总生存率和无事件生存率;(2)评估安全性:是否存在导致治疗中断或死亡的不良反应。
100%的患者出现完全血液学缓解,90.9%出现主要细胞遗传学缓解,48.5%出现完全细胞遗传学缓解。36.4%的患者出现分子反应。在平均 39 个月的随访中,总生存率为 96%,估计五年无事件生存率为 85%。39.5%的患者没有发生不良反应。最常见的不良反应是骨髓抑制(24.2%)和消化系统紊乱(21.2%)。其次是水肿,主要是眶周水肿(9.1%)、皮肤色素减退(3%)和心律失常(3%)。
在本研究中,伊马替尼是新诊断的慢性髓性白血病患者的有效一线治疗药物,总生存率和无事件生存率都得到了证实。没有观察到严重的不良反应。