Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Am J Hematol. 2021 Aug 1;96(8):1000-1007. doi: 10.1002/ajh.26238. Epub 2021 May 28.
Relapsed/refractory (R/R) Philadelphia chromosome positive acute lymphoblastic leukemia (Ph + ALL) and lymphoid blast phase of chronic myeloid leukemia (LBP-CML) have poor outcomes. We designed a phase 1/2 study combining inotuzumab ozogamicin with bosutinib for this patient population. Patients with T315I mutation were excluded. Bosutinib was administered daily at three dose levels (300 mg/d, 400 mg/d, 500 mg/d) in a 3 + 3 design. Inotuzumab ozogamicin was dosed weekly during cycle one, and once every 4 weeks subsequently for a total of six cycles. The primary objective was to determine the safety and the maximum tolerated dose (MTD) of bosutinib in combination with inotuzumab ozogamicin. Eighteen patients were enrolled (Ph-positive ALL, n = 16; LBP-CML, n = 2). The median age was 62 years (range, 19-74) and the median number of prior therapies was one (range, 1-5). Dose limiting toxicities included grade 3 skin rash and bosutinib 400 mg daily was determined as the MTD. The most frequent grade 3/4 treatment-emergent adverse events were thrombocytopenia (60%) and neutropenia (38%). A complete response (CR) / CR with incomplete count recovery (CRi) was achieved in 15/18 (83%) patients; 11/18 (61%) patients achieved negative measurable residual disease by flow cytometry. Complete molecular response was noted in 10/18 (56%) patients. The 30-day mortality was 0%. After a median follow-up of 44 months, the median duration of response and overall survival were 7.7 months and 13.5 months, respectively. Six patients had a subsequent allogeneic stem cell transplant. No patient developed veno-occlusive disease. Inotuzumab ozogamicin with bosutinib was well tolerated in R/R Ph-positive ALL and LBP-CML.
复发/难治性费城染色体阳性急性淋巴细胞白血病 (Ph+ALL) 和慢性髓性白血病的淋巴母细胞期 (LBP-CML) 预后较差。我们设计了一项 1/2 期研究,将英妥昔单抗奥佐米星与博舒替尼联合用于这一患者人群。排除 T315I 突变患者。博舒替尼以 3+3 设计在三个剂量水平(300mg/d、400mg/d、500mg/d)下每日给药。英妥昔单抗奥佐米星在第一个周期每周给药一次,随后每 4 周给药一次,共 6 个周期。主要目的是确定博舒替尼联合英妥昔单抗奥佐米星的安全性和最大耐受剂量 (MTD)。共纳入 18 例患者(Ph+ALL,n=16;LBP-CML,n=2)。中位年龄为 62 岁(范围,19-74 岁),中位治疗线数为 1 线(范围,1-5 线)。剂量限制毒性包括 3 级皮疹,确定博舒替尼 400mg/d 为 MTD。最常见的 3/4 级治疗相关不良事件为血小板减少症(60%)和中性粒细胞减少症(38%)。18 例患者中有 15 例(83%)达到完全缓解(CR)/不完全血细胞计数恢复的完全缓解(CRi);18 例患者中有 11 例(61%)通过流式细胞术检测到阴性可测量残留疾病。18 例患者中有 10 例(56%)达到完全分子缓解。30 天死亡率为 0%。中位随访 44 个月后,中位缓解持续时间和总生存期分别为 7.7 个月和 13.5 个月。6 例患者随后进行了异基因造血干细胞移植。无患者发生静脉闭塞性疾病。英妥昔单抗奥佐米星联合博舒替尼在复发/难治性 Ph+ALL 和 LBP-CML 中耐受良好。