Washington University School of Medicine, St. Louis, Missouri.
Duke Cancer Institute, Duke University, Durham, North Carolina.
Clin Cancer Res. 2024 Nov 15;30(22):5042-5052. doi: 10.1158/1078-0432.CCR-24-1547.
Seizure-related homolog protein 6 (SEZ6) is a novel target expressed in small cell lung cancer (SCLC). ABBV-011, a SEZ6-targeted antibody conjugated to calicheamicin, was evaluated in a phase I study (NCT03639194) in patients with relapsed/refractory SCLC. We report initial outcomes of ABBV-011 monotherapy.
ABBV-011 was administered intravenously once every 3 weeks during dose escalation (0.3-2 mg/kg) and expansion. Patients with SEZ6-positive tumors (≥25% of tumor cells with ≥1+ staining intensity by IHC) were preselected for expansion. Safety, tolerability, antitumor activity, and pharmacokinetics were evaluated.
As of August 2022, 99 patients received ABBV-011 monotherapy [dose escalation, n = 36; Japanese dose evaluation, n = 3; dose expansion, n = 60 (1 mg/kg, n = 40)]; the median age was 63 years (range, 41-79 years). Also, 32%, 41%, and 26% of patients received 1, 2, and ≥3 prior therapies, respectively. The maximum tolerated dose was not reached through 2.0 mg/kg. The most common treatment-emergent adverse events were fatigue (50%), nausea (42%), and thrombocytopenia (41%). The most common hepatic treatment-emergent adverse events were increased aspartate aminotransferase (22%), increased γ-glutamyltransferase (21%), and hyperbilirubinemia (17%); two patients experienced veno-occlusive liver disease. The objective response rate was 19% (19/98). In the 1-mg/kg dose-expansion cohort (n = 40), the objective response rate was 25%; the median response duration was 4.2 months (95% confidence interval, 2.6-6.7); and the median progression-free survival was 3.5 months (95% confidence interval, 1.5-4.2).
ABBV-011 1.0 mg/kg every 3 weeks monotherapy was well tolerated and demonstrated encouraging antitumor activity in heavily pretreated patients with relapsed/refractory SCLC. SEZ6 is a promising novel SCLC target and warrants further investigation.
SEZ6 是一种新型小细胞肺癌(SCLC)靶标蛋白。ABBV-011 是一种靶向 SEZ6 的抗体药物偶联物,与加利车霉素偶联,在复发/难治性 SCLC 患者中进行了 I 期研究(NCT03639194)。我们报告 ABBV-011 单药治疗的初步结果。
ABBV-011 在剂量递增(0.3-2mg/kg)和扩展阶段每 3 周静脉输注一次。选择 SEZ6 阳性肿瘤(IHC 染色强度≥1+的肿瘤细胞≥25%)的患者进行扩展。评估安全性、耐受性、抗肿瘤活性和药代动力学。
截至 2022 年 8 月,99 例患者接受 ABBV-011 单药治疗[剂量递增,n=36;日本剂量评估,n=3;剂量扩展,n=60(1mg/kg,n=40)];中位年龄为 63 岁(范围,41-79 岁)。此外,32%、41%和 26%的患者分别接受了 1、2 和≥3 次既往治疗。2.0mg/kg 未达到最大耐受剂量。最常见的治疗相关不良事件是疲劳(50%)、恶心(42%)和血小板减少症(41%)。最常见的肝脏治疗相关不良事件是天冬氨酸转氨酶升高(22%)、γ-谷氨酰转移酶升高(21%)和高胆红素血症(17%);两名患者发生静脉闭塞性肝病。客观缓解率为 19%(19/98)。在 1mg/kg 剂量扩展队列(n=40)中,客观缓解率为 25%;中位缓解持续时间为 4.2 个月(95%置信区间,2.6-6.7);中位无进展生存期为 3.5 个月(95%置信区间,1.5-4.2)。
ABBV-011 1.0mg/kg,每 3 周单药治疗耐受性良好,在复发/难治性 SCLC 患者中具有令人鼓舞的抗肿瘤活性。SEZ6 是一种很有前途的新型 SCLC 靶标,值得进一步研究。