Abruzzese Elisabetta, Gozzetti Alessandro, Galimberti Sara, Trawinska Malgorzata Monika, Caravita Tommaso, Siniscalchi Agostina, Cervetti Giulia, Mauriello Alessandro, Coletta Angela Maria, De Fabritiis Paolo
Hematology, S. Eugenio Hospital, University Tor Vergata, Rome, Italy.
Cancer. 2007 Jun 15;109(12):2466-72. doi: 10.1002/cncr.22699.
Imatinib is a tyrosine kinase-specific inhibitor widely used for the treatment of chronic myeloid leukemia (CML). Studies reported the occurrence of additional cytogenetic abnormalities in the Philadelphia chromosome (Ph)-negative cell population emerging after treatment-induced suppression of the Ph-positive clone. These abnormalities were described in a relatively high proportion of patients treated with imatinib compared with the anecdotal reports of similar cases in patients treated with other drugs. However, the origin of these abnormalities as well as their biological and clinical significance are unknown.
The study involved 13 cases of patients diagnosed with CML carrying cytogenetic abnormalities in their Ph-negative cell population after imatinib treatment. The presence of the markers within the CD34+ stem cell compartment and the cell culture growth were analyzed and patients were followed over time.
CD34+ cells express the cytogenetic markers present in Ph- cells, suggesting a possible involvement of the stem cell population. Cultured cells showed normal growth in all but 1 patient. No growth advantage was demonstrated for the Ph-negative or the Ph-positive clone after cell culture.
After follow-up of up to 49 months, none of the patients had evolved to myelodysplasia or acute leukemia. Hypothesis regarding the biological and clinical significance of these abnormalities are formulated.
伊马替尼是一种酪氨酸激酶特异性抑制剂,广泛用于治疗慢性髓性白血病(CML)。研究报道,在治疗诱导的Ph阳性克隆受到抑制后出现的费城染色体(Ph)阴性细胞群体中,会出现额外的细胞遗传学异常。与使用其他药物治疗的类似病例的轶事报道相比,这些异常在接受伊马替尼治疗的患者中出现的比例相对较高。然而,这些异常的起源及其生物学和临床意义尚不清楚。
该研究纳入了13例伊马替尼治疗后Ph阴性细胞群体中存在细胞遗传学异常的CML患者。分析了CD34+干细胞区室中标志物的存在情况以及细胞培养生长情况,并对患者进行了长期随访。
CD34+细胞表达Ph阴性细胞中存在的细胞遗传学标志物,提示干细胞群体可能参与其中。除1例患者外,培养的细胞均显示正常生长。细胞培养后,Ph阴性或Ph阳性克隆均未显示出生长优势。
经过长达49个月的随访,没有患者进展为骨髓增生异常或急性白血病。针对这些异常的生物学和临床意义提出了假设。