Hanley Michael J, Larson Thomas R, Diderichsen Paul M, Largajolli Anna, Hui Katrina, Srimani Jaydeep, Wang Bingxia, Vorog Alexander, Gupta Neeraj
Takeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.
Certara, Radnor, Pennsylvania, USA.
Clin Transl Sci. 2025 Mar;18(3):e70175. doi: 10.1111/cts.70175.
In March 2024, ponatinib received accelerated FDA approval for the treatment of newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph + ALL) in combination with chemotherapy based on the Phase 3 PhALLCON study (NCT03589326), which demonstrated a higher rate of minimal residual disease (MRD)-negative complete remission (CR) at the end of induction (EOI) with ponatinib (34.4%) versus imatinib (16.7%; p = 0.002). Patients received ponatinib (30 mg QD with reduction to 15 mg QD upon achievement of MRD-negative CR at EOI) or imatinib (600 mg QD) combined with 20 cycles of reduced-intensity chemotherapy (induction: 3 cycles; consolidation: 6 cycles; and maintenance: 11 cycles). Ponatinib pharmacokinetics (PK) were similar in patients in PhALLCON and patients in a previous population PK analysis. Bayesian re-estimation of the previously developed population PK model adequately described PhALLCON PK data. Exposure-efficacy analyses did not identify a significant relationship between ponatinib exposure and the probability of MRD-negative CR at EOI (p = 0.619), suggesting a consistent efficacy benefit across exposures. Ponatinib exposure was not a significant predictor of arterial occlusive events, venous thromboembolic events, thrombocytopenia, or lipase increase (p > 0.05). However, higher exposures were associated with a higher probability of hypertension (p = 0.0340) and alanine aminotransferase (ALT) increase (p = 0.0034). Dose reduction from 30 to 15 mg was predicted to decrease the odds of experiencing hypertension by 37.7% and ALT increase by 44.2%. Collectively, exposure-response analyses support a favorable benefit-risk profile of the approved ponatinib dosage (30 mg QD reduced to 15 mg QD upon achievement of MRD-negative CR at EOI), combined with chemotherapy, for frontline treatment of Ph + ALL.
2024年3月,基于3期PhALLCON研究(NCT03589326),普纳替尼获得美国食品药品监督管理局(FDA)加速批准,与化疗联合用于治疗新诊断的费城染色体阳性急性淋巴细胞白血病(Ph+ALL)。该研究表明,在诱导结束时,接受普纳替尼治疗的患者微小残留病(MRD)阴性完全缓解(CR)率更高(34.4%),而接受伊马替尼治疗的患者为16.7%(p = 0.002)。患者接受普纳替尼(30mg每日一次,在诱导结束时达到MRD阴性CR后减至15mg每日一次)或伊马替尼(600mg每日一次),并联合20个周期的低强度化疗(诱导:3个周期;巩固:6个周期;维持:11个周期)。PhALLCON研究中的患者与先前群体药代动力学分析中的患者的普纳替尼药代动力学(PK)相似。对先前建立的群体PK模型进行贝叶斯重新估计,充分描述了PhALLCON的PK数据。暴露-疗效分析未发现普纳替尼暴露与诱导结束时MRD阴性CR概率之间存在显著关系(p = 0.619),这表明在不同暴露水平下疗效获益一致。普纳替尼暴露不是动脉闭塞事件、静脉血栓栓塞事件、血小板减少或脂肪酶升高的显著预测因素(p > 0.05)。然而,较高的暴露水平与高血压概率增加(p = 0.0340)和丙氨酸转氨酶(ALT)升高(p = 0.0034)相关。预计将剂量从30mg减至15mg可使高血压发生几率降低37.7%,ALT升高几率降低44.2%。总体而言,暴露-反应分析支持了获批的普纳替尼剂量(30mg每日一次,在诱导结束时达到MRD阴性CR后减至15mg每日一次)与化疗联合用于Ph+ALL一线治疗时具有良好的获益-风险特征。