Service d'Hématologie et Oncologie Biologique, CHU de Poitiers, Poitiers, France.
Blood. 2011 Sep 29;118(13):3657-60. doi: 10.1182/blood-2011-02-335497. Epub 2011 Jul 25.
Sustained undetectable molecular residual disease (UMRD) is obtained in a minority of patients with chronic myeloid leukemia treated with tyrosine kinase inhibitors. It remains unclear whether these patients are definitively cured of their leukemia or whether leukemic stem cells (LSCs) persist in their BM. We have evaluated the presence of BCR-ABL-expressing marrow LSCs in 6 patients with chronic myeloid leukemia with sustained UMRD induced by IFN-α (n = 3), imatinib mesylate after IFN-α failure (n = 2), and dasatinib after imatinib intolerance (n = 1). Purified CD34(+) cells were used for clonogenic and long-term culture-initiating cell assays performed on classic or HOXB4-expressing MS-5 feeders. Using this strategy, we identified BCR-ABL-expressing LSCs in all patients. Interestingly, long-term culture-initiating cell assays with MS-5/HOXB4 stromal feeders increased detected numbers of LSCs in 3 patients. The relation between LSC persistency and a potential risk of disease relapse for patients with durable UMRD (on or off tyrosine kinase inhibitor therapy) warrants further investigation.
在接受酪氨酸激酶抑制剂治疗的慢性髓性白血病患者中,少数患者可获得持续不可检测的分子残留疾病(UMRD)。目前尚不清楚这些患者是否已从白血病中得到明确治愈,还是白血病干细胞(LSCs)仍存在于骨髓中。我们评估了 6 例慢性髓性白血病患者的骨髓 LSCs 中是否存在 BCR-ABL 表达,这些患者的 UMRD 是由 IFN-α(n = 3)、IFN-α 失败后使用甲磺酸伊马替尼(n = 2)和伊马替尼不耐受后使用达沙替尼(n = 1)诱导的。使用经典或表达 HOXB4 的 MS-5 饲养细胞进行集落形成和长期培养起始细胞测定,纯化 CD34+细胞。使用这种策略,我们在所有患者中均鉴定到表达 BCR-ABL 的 LSCs。有趣的是,用 MS-5/HOXB4 基质饲养细胞进行长期培养起始细胞测定增加了 3 名患者中 LSC 的检测数量。在持续 UMRD(酪氨酸激酶抑制剂治疗或停药)的患者中,LSC 持续性与疾病复发的潜在风险之间的关系需要进一步研究。