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 Journal Article


Authors: Morgensztern, D.; Ready, N.; Johnson, M. L.; Dowlati, A.; Choudhury, N.; Carbone, D. P.; Schaefer, E.; Arnold, S. M.; Puri, S.; Piotrowska, Z.; Hegde, A.; Chiang, A. C.; Iams, W.; Tolcher, A.; Nosaki, K.; Kozuki, T.; Li, T.; Santana-Davila, R.; Akamatsu, H.; Murakami, H.; Yokouchi, H.; Wang, S.; Zha, J.; Li, R.; Robinson, R. R.; Hingorani, P.; Jeng, E. E.; Furqan, M.
Article Title: 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
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. ©2024 The Authors; Published by the American Association for Cancer Research.
Keywords: adult; aged; aged, 80 and over; middle aged; clinical trial; lung neoplasms; pathology; monoclonal antibody; lung tumor; multicenter study; maximum tolerated dose; phase 1 clinical trial; drug therapy; small cell lung cancer; small cell lung carcinoma; antibody conjugate; immunoconjugates; antibodies, monoclonal, humanized; very elderly; humans; human; male; female
Journal Title: Clinical Cancer Research
Volume: 30
Issue: 22
ISSN: 1078-0432
Publisher: American Association for Cancer Research  
Date Published: 2024-11-15
Start Page: 5042
End Page: 5052
Language: English
DOI: 10.1158/1078-0432.Ccr-24-1547
PUBMED: 39287821
PROVIDER: scopus
PMCID: PMC11565168
DOI/URL:
Notes: Article -- Source: Scopus
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