Oxford University Hospitals NHS Foundation Trust, Churchill Cancer Center, Oxford, UK.
Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Future Oncol. 2022 Nov;18(36):3961-3969. doi: 10.2217/fon-2022-0976. Epub 2022 Nov 15.
Treatment with covalent Bruton tyrosine kinase inhibitors (BTKi) represents an important advance in the management of relapsed or refractory mantle cell lymphoma, but these treatments are not curative and many patients ultimately relapse. Pirtobrutinib, a highly selective, noncovalent (reversible) BTKi, inhibits both wild type and C481-mutant BTK with equal low nM potency, and has favorable oral pharmacology that enables continuous BTK inhibition throughout the dosing interval regardless of intrinsic rate of BTK turnover. Pirtobrutinib is well tolerated and has demonstrated promising efficacy in patients with poor prognosis B-cell malignancies following prior therapy, including covalent BTKi. This phase III, head-to-head, randomized study (NCT04662255) will evaluate whether pirtobrutinib is superior to investigator's choice of covalent BTKi in patients with previously treated, BTKi-naive mantle cell lymphoma.
使用共价 Bruton 酪氨酸激酶抑制剂 (BTKi) 治疗复发或难治性套细胞淋巴瘤是一项重要进展,但这些治疗方法无法治愈,许多患者最终会复发。Pirtobrutinib 是一种高度选择性、非共价(可逆)BTKi,对野生型和 C481 突变型 BTK 具有相同的低纳摩尔效力,具有良好的口服药代动力学特性,可在整个给药间隔内持续抑制 BTK,无论 BTK 周转率的内在速率如何。Pirtobrutinib 耐受性良好,在先前接受治疗的包括共价 BTKi 在内的预后不良 B 细胞恶性肿瘤患者中显示出有前景的疗效。这项 III 期头对头、随机研究(NCT04662255)将评估 pirtobrutinib 是否优于先前接受治疗、BTKi 初治的套细胞淋巴瘤患者的研究者选择的共价 BTKi。