Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Section of Molecular Hematology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Am J Hematol. 2020 Nov;95(11):1296-1303. doi: 10.1002/ajh.25943. Epub 2020 Aug 19.
Stroma-leukemia interactions mediated by CXCR4, CD44, VLA4, and their respective ligands contribute to therapy resistance in FLT3-ITD-mutated acute myelogenous leukemia (AML). We conducted a phase 1 study with the combination of sorafenib (a FLT3-ITD inhibitor), plerixafor (a SDF-1/CXCR4 inhibitor), and G-CSF (that cleaves SDF-1, CD44, and VLA4). Twenty-eight patients with relapsed/refractory FLT3-ITD-mutated AML were enrolled from December 2010 to December 2013 at three dose levels of sorafenib (400, 600, and 800 mg twice daily) and G-CSF and plerixafor were administered every other day for seven doses starting on day one. Sorafenib 800 mg twice daily was selected for the expansion phase. While no dose-limiting toxicities (DLT) were encountered in the four-week DLT window, hand-foot syndrome and rash were seen beyond the DLT window, which required dose reductions in most patients. The response rate was 36% (complete response (CR) = 4, complete remission with incomplete platelet recovery (CRp) = 4, complete remission with incomplete hematologic recovery (CRi) = 1, and partial response (PR) = 1) for the intention to treat population. Treatment resulted in 58.4 and 47 mean fold mobilization of blasts and CD34 /38- stem/progenitor cells, respectively, to the circulation. Expression of the adhesion molecules CXCR4, CD44, and VLA4 on circulating leukemia cells correlated negatively with the mobilization of CD34+/38-, CD34+/38-/123+ "progenitor" cells (all P ≤ .002). Mass cytometry analysis of sequential samples from two patients demonstrated resistance emerging early on from sub-clones with persistent Akt and/or ERK signaling. In conclusion, the strategy of combined inhibition of FLT3 kinase and stromal adhesive interactions has promising activity in relapsed/refractory, FLT3-ITD-mutated AML, which warrants further evaluation in the front-line setting.
CXCR4、CD44、VLA4 及其各自配体介导的基质-白血病相互作用导致 FLT3-ITD 突变的急性髓系白血病(AML)对治疗产生耐药性。我们进行了一项Ⅰ期研究,联合使用索拉非尼(FLT3-ITD 抑制剂)、plerixafor(SDF-1/CXCR4 抑制剂)和 G-CSF(可裂解 SDF-1、CD44 和 VLA4)。2010 年 12 月至 2013 年 12 月,在三个索拉非尼剂量水平(400、600 和 800mg 每日两次)和 G-CSF 和 plerixafor 的情况下,共招募了 28 例复发性/难治性 FLT3-ITD 突变的 AML 患者,从第 1 天开始,每两天给予 7 剂。选择索拉非尼 800mg 每日两次进行扩展阶段。虽然在四周的 DLT 窗口期内未发现剂量限制性毒性(DLT),但在 DLT 窗口期之外出现手足综合征和皮疹,大多数患者需要减少剂量。意向治疗人群的反应率为 36%(完全缓解(CR)=4,不完全血小板恢复的完全缓解(CRp)=4,不完全血液学恢复的完全缓解(CRi)=1,部分缓解(PR)=1)。治疗导致循环中 blast 和 CD34+/38-干细胞/祖细胞分别平均增加 58.4 和 47 倍。循环白血病细胞上粘附分子 CXCR4、CD44 和 VLA4 的表达与 CD34+/38-、CD34+/38-/123+“祖细胞”的动员呈负相关(均 P≤.002)。两名患者的连续样本的质谱流式细胞术分析表明,早期就从持续存在 Akt 和/或 ERK 信号的亚克隆中出现耐药性。总之,联合抑制 FLT3 激酶和基质黏附相互作用的策略在复发性/难治性、FLT3-ITD 突变的 AML 中具有有前景的活性,值得在一线治疗中进一步评估。