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索拉非尼、G-CSF 和普乐沙福联合治疗复发性/难治性 FLT3-ITD 突变型急性髓系白血病患者的 1 期研究。

Phase 1 study of combinatorial sorafenib, G-CSF, and plerixafor treatment in relapsed/refractory, FLT3-ITD-mutated acute myelogenous leukemia patients.

机构信息

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.

出版信息

Am J Hematol. 2020 Nov;95(11):1296-1303. doi: 10.1002/ajh.25943. Epub 2020 Aug 19.

Abstract

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.

摘要

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。

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