Journal article
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
Clinical cancer research, Vol.30(22), pp.5042-5052
11/15/2024
DOI: 10.1158/1078-0432.CCR-24-1547
PMCID: PMC11565168
PMID: 39287821
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 (Q3W) during dose escalation (0.3-2 mg/kg) and expansion. Patients with SEZ6-positive tumors (≥25% of tumor cells with ≥1+ staining intensity by immunohistochemistry) 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]); median age was 63 years (range, 41-79). Thirty-two percent, 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. Most common treatment-emergent adverse events (TEAEs) were fatigue (50%), nausea (42%), and thrombocytopenia (41%). Most common hepatic TEAEs were increased aspartate aminotransferase (22%), increased g-glutamyltransferase (21%), and hyperbilirubinemia (17%); 2 patients experienced veno-occlusive liver disease. Objective response rate (ORR) was 19% (19/98). In the 1-mg/kg dose-expansion cohort (n=40), ORR was 25%; median response duration was 4.2 months (95% CI, 2.6-6.7) and median progression-free survival was 3.5 months (95% CI, 1.5-4.2). CONCLUSIONS: ABBV-011 1.0 mg/kg Q3W 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.
Details
- Title: Subtitle
- 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
- Creators
- Daniel Morgensztern - Washington University in St. Louis School of MedicineNeal Ready - Duke UniversityMelissa Johnson - Tennessee OncologyAfshin Dowlati - University Hospitals Seidman Cancer CenterNoura Choudhury - Memorial Sloan Kettering Cancer CenterDavid Carbone - The Ohio State UniversityEric Schaefer - Highlands Oncology GroupSusanne Arnold - University of KentuckySonam Puri - Huntsman Cancer InstituteZofia Piotrowska - Massachusetts General HospitalAparna Hegde - University of Alabama at BirminghamAnne Chiang - Yale School of MedicineWade Iams - Vanderbilt University Medical CenterAnthony TolcherKaname Nosaki - National Cancer Center Hospital EastToshiyuki Kozuki - National Hospital OrganizationTianhong Li - University of California Davis Medical CenterRafael Santana-Davila - University of WashingtonHiroaki Akamatsu - Wakayama Medical UniversityHaruyasu Murakami - Shizuoka Cancer CenterHiroshi Yokouchi - National Hospital OrganizationSong Wang - AbbVie (United States)Jiuhong Zha - AbbVie (United States)Rui Li - AbbVie (United States)Randy Robinson - AbbVie (United States)Pooja Hingorani - AbbVie (United States)Edwin Jeng - AbbVie (United States)Muhammad Furqan - University of Iowa
- Resource Type
- Journal article
- Publication Details
- Clinical cancer research, Vol.30(22), pp.5042-5052
- DOI
- 10.1158/1078-0432.CCR-24-1547
- PMID
- 39287821
- PMCID
- PMC11565168
- NLM abbreviation
- Clin Cancer Res
- ISSN
- 1078-0432
- eISSN
- 1557-3265
- Publisher
- American Association for Cancer Research; PHILADELPHIA
- Grant note
- AbbVie, Inc.
AbbVie, Inc. funded this study and participated in the study design, research, analysis, data collection, interpretation of data, reviewing, and approval of the publication. AbbVie and the authors thank the participants, study sites, and investigators who participated in this clinical trial. Medical writing support was provided by Iratxe Abarrategui, PhD, CMPP, of Aptitude Health, The Hague, the Netherlands, and funded by AbbVie. All authors had access to relevant data and participated in the drafting, review, and approval of this publication. No honoraria or payments were made for authorship.
- Language
- English
- Electronic publication date
- 09/17/2024
- Date published
- 11/15/2024
- Academic Unit
- Hematology, Oncology, and Blood & Marrow Transplantation; Internal Medicine
- Record Identifier
- 9984751755902771
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