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ABBV-011 是一种与癫痫相关的同源蛋白 6 靶向抗体药物偶联物,在小细胞肺癌患者中的 I 期首次人体研究。

A Phase I First-in-Human Study of ABBV-011, a Seizure-Related Homolog Protein 6-Targeting Antibody-Drug Conjugate, in Patients with Small Cell Lung Cancer.

机构信息

Washington University School of Medicine, St. Louis, Missouri.

Duke Cancer Institute, Duke University, Durham, North Carolina.

出版信息

Clin Cancer Res. 2024 Nov 15;30(22):5042-5052. doi: 10.1158/1078-0432.CCR-24-1547.

Abstract

PURPOSE

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.

PATIENTS AND METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

目的

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。

患者和方法

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。

结果

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)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2af/11565168/155fdb726ec4/ccr-24-1547_f1.jpg

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