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lintuzumab-Ac225联合CLAG-M挽救疗法用于复发/难治性急性髓系白血病的1期研究

Phase 1 study of lintuzumab-Ac225 combined with CLAG-M salvage therapy in relapsed/refractory acute myeloid leukemia.

作者信息

Abedin Sameem M, Guru Murthy Guru Subramanian, Hamadani Mehdi, Michaelis Laura C, Carlson Karen-Sue, Runaas Lyndsey, Gauger Katelyn, Desai Avinash G, Chen Mary M, Li Kate L, Rotibi Mojisola, Syed Umar, Vusirikala Madhuri, Harrington Alexandra, Atallah Ehab L

机构信息

Division of Hematology/Oncology, Medical College of Wisconsin, Milwaukee, WI, USA.

Actinium Pharmaceuticals, New York, NY, USA.

出版信息

Leukemia. 2025 Apr;39(4):837-843. doi: 10.1038/s41375-025-02528-3. Epub 2025 Feb 15.

Abstract

Lintuzumab-Ac255 is a humanized anti-CD33 antibody linked to Actinium-225 delivering high-energy alpha-particles to leukemia cells, inciting double-strand DNA breaks and cell death. This phase 1 study assessed the safety and efficacy of lintuzumab-Ac225 after CLAG-M salvage therapy in patients with relapsed/refractory acute myeloid leukemia (R/R AML). Primary objectives were determination of maximum tolerated dose (MTD), recommended phase 2 dose (RP2D), and safety. Using a 3 + 3 dose-escalation design, 21 patients were enrolled sequentially into 4 cohorts to receive a lintuzumab-Ac225 infusion (0.25-1.0 µCi/kg) 7 ( + 2) days after CLAG-M (days 1-6); 5 additional patients received the RP2D. Of evaluable patients, 86.7% had high-risk disease. The MTD and RP2D was 0.75 µCi/kg. Common grade 3/4 adverse events were febrile neutropenia (65.4%) and decreased white blood cells (50%). The composite complete remission (CRc) rates (CR/CRi) were 56.6% overall, 50% in patients with mutated TP53, and 38.5% in prior venetoclax-treated patients. Measurable residual disease (MRD)-negativity was achieved in 8 of 12 responders. Among all patients (n = 26), estimated 2-year OS was 23.1% (95% CI, 9.4-40.3) and estimated 1-year PFS was 30.8% (95% CI, 14.6-48.5). Lintuzumab-Ac225 plus CLAG-M was well tolerated with expected, manageable toxicities, while yielding deep and meaningful responses in high-risk R/R AML patients.

摘要

林妥珠单抗 - Ac255是一种人源化抗CD33抗体,与锕 - 225连接,可向白血病细胞递送高能α粒子,引发双链DNA断裂和细胞死亡。这项1期研究评估了林妥珠单抗 - Ac225在复发/难治性急性髓系白血病(R/R AML)患者接受CLAG - M挽救治疗后的安全性和疗效。主要目标是确定最大耐受剂量(MTD)、推荐的2期剂量(RP2D)和安全性。采用3 + 3剂量递增设计,21例患者依次入组4个队列,在CLAG - M(第1 - 6天)后7(±2)天接受林妥珠单抗 - Ac225输注(0.25 - 1.0 μCi/kg);另外5例患者接受RP2D。在可评估的患者中,86.7%患有高危疾病。MTD和RP2D为0.75 μCi/kg。常见的3/4级不良事件为发热性中性粒细胞减少(65.4%)和白细胞减少(50%)。总体复合完全缓解(CRc)率(CR/CRi)为56.6%,TP53突变患者为50%,既往接受维奈克拉治疗的患者为38.5%。12例缓解者中有8例实现了微小残留病(MRD)阴性。在所有患者(n = 26)中,估计2年总生存率(OS)为23.1%(95%CI,9.4 - 40.3),估计1年无进展生存率(PFS)为30.8%(95%CI,14.6 - 48.5)。林妥珠单抗 - Ac225联合CLAG - M耐受性良好,毒性预期且可控,同时在高危R/R AML患者中产生了深度且有意义的缓解。

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