Baccarani M, Ruggero D, Tura S
Boll Ist Sieroter Milan. 1978 Jul 31;57(3):278-88.
Current therapies of chronic myeloid leukemia (CML) do not prevent the progression of the disease towards blastic metamorphosis, and have not resulted in a remarkable prolongation of survival. Splenectomy was proposed with the aim of removing a part of the tumor without cytotoxics and of removing a potentially privileged pool of malignant blast cells. Acute leukemia-like chemotherapy was proposed with the aim of eradicating or better controlling the highly malignant subclones that emerge during the chronic phase. A preliminary analysis of 2 clinical trials these therapeutic measures, suggests that splenectomy does not modify the rate of blastic transformation, during the first 2 to 3 years from diagnosis. Also the rate of blastic transformation is similar for patients receiving hydroxyurea at first, and arabinosyl cytosine (ARA-C), vincristine (VCR) and prednisone (P) thereafter, as for patients receiving from the clinical onset of CML a more intensive chemotherapy with ARA-C, thioguanine (TG) and daunomycin (DAUNO), but not VCR + P.
慢性髓性白血病(CML)的现有疗法无法阻止疾病向原始细胞转化阶段进展,也未显著延长生存期。脾切除术的提出旨在在不使用细胞毒性药物的情况下切除部分肿瘤,并去除潜在的恶性原始细胞特权池。急性白血病样化疗的提出旨在根除或更好地控制慢性期出现的高恶性亚克隆。对这两种治疗措施的2项临床试验进行的初步分析表明,脾切除术在诊断后的头2至3年内不会改变原始细胞转化的速率。同样,起初接受羟基脲治疗、之后接受阿糖胞苷(ARA-C)、长春新碱(VCR)和泼尼松(P)治疗的患者,与从CML临床发病开始就接受更强化的阿糖胞苷、硫鸟嘌呤(TG)和柔红霉素(DAUNO)化疗(而非VCR + P)的患者相比,原始细胞转化速率相似。