Department of Hematology, Goethe University, Frankfurt, Germany.
1] Fusion Pharma, LLC, Moscow, Russian Federation [2] Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation.
Leukemia. 2015 May;29(5):1104-14. doi: 10.1038/leu.2014.326. Epub 2014 Nov 14.
Targeting BCR/ABL with tyrosine kinase inhibitors (TKIs) is a proven concept for the treatment of Philadelphia chromosome-positive (Ph+) leukemias. Resistance attributable to either kinase mutations in BCR/ABL or nonmutational mechanisms remains the major clinical challenge. With the exception of ponatinib, all approved TKIs are unable to inhibit the 'gatekeeper' mutation T315I. However, a broad spectrum of kinase inhibition increases the off-target effects of TKIs and may be responsible for cardiovascular issues of ponatinib. Thus, there is a need for more selective options for the treatment of resistant Ph+ leukemias. PF-114 is a novel TKI developed with the specifications of (i) targeting T315I and other resistance mutations in BCR/ABL; (ii) achieving a high selectivity to improve safety; and (iii) overcoming nonmutational resistance in Ph+ leukemias. PF-114 inhibited BCR/ABL and clinically important mutants including T315I at nanomolar concentrations. It suppressed primary Ph+ acute lymphatic leukemia-derived long-term cultures that either displayed nonmutational resistance or harbor the T315I. In BCR/ABL- or BCR/ABL-T315I-driven murine leukemia as well as in xenograft models of primary Ph+ leukemia harboring the T315I, PF-114 significantly prolonged survival to a similar extent as ponatinib. Our work supports clinical evaluation of PF-114 for the treatment of resistant Ph+ leukemia.
针对费城染色体阳性(Ph+)白血病,用酪氨酸激酶抑制剂(TKIs)靶向 BCR/ABL 是一种已被证实的治疗方法。由于 BCR/ABL 中的激酶突变或非突变机制导致的耐药性仍然是主要的临床挑战。除了 ponatinib 外,所有批准的 TKI 都无法抑制“守门员”突变 T315I。然而,广泛的激酶抑制会增加 TKI 的脱靶效应,并且可能是 ponatinib 心血管问题的原因。因此,需要更具选择性的治疗耐药 Ph+白血病的方法。PF-114 是一种新型 TKI,具有以下特点:(i)靶向 BCR/ABL 中的 T315I 和其他耐药突变;(ii)实现高选择性以提高安全性;(iii)克服 Ph+白血病中的非突变耐药性。PF-114 以纳摩尔浓度抑制 BCR/ABL 和临床相关的突变体,包括 T315I。它抑制了表现出非突变耐药性或携带 T315I 的原发性 Ph+急性淋巴细胞白血病衍生的长期培养物。在 BCR/ABL 或 BCR/ABL-T315I 驱动的小鼠白血病以及携带 T315I 的原发性 Ph+白血病的异种移植模型中,PF-114 显著延长了生存时间,与 ponatinib 相似。我们的工作支持 PF-114 用于治疗耐药 Ph+白血病的临床评估。