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Safety and activity of the first-in-class locked nucleic acid (LNA) miR-221 selective inhibitor in refractory advanced cancer patients: a first-in-human, phase 1, open-label, dose-escalation study.

Authors :
Tassone P
Di Martino MT
Arbitrio M
Fiorillo L
Staropoli N
Ciliberto D
Cordua A
Scionti F
Bertucci B
Salvino A
Lopreiato M
Thunarf F
Cuomo O
Zito MC
De Fina MR
Brescia A
Gualtieri S
Riillo C
Manti F
Caracciolo D
Barbieri V
Di Paola ED
Di Francesco AE
Tagliaferri P
Source :
Journal of hematology & oncology [J Hematol Oncol] 2023 Jun 26; Vol. 16 (1), pp. 68. Date of Electronic Publication: 2023 Jun 26.
Publication Year :
2023

Abstract

Background: We developed a 13-mer locked nucleic acid (LNA) inhibitor of miR-221 (LNA-i-miR-221) with a full phosphorothioate (PS)-modified backbone. This agent downregulated miR-221, demonstrated anti-tumor activity against human xenografts in mice, and favorable toxicokinetics in rats and monkeys. Allometric interspecies scaling allowed us to define the first-in-class LNA-i-miR-221 safe starting dose for the clinical translation.<br />Methods: In this first-in-human, open-label, dose-escalation phase 1 trial, we enrolled progressive cancer patients (aged ≥ 18 years) with ECOG 0-2 into 5 cohorts. The treatment cycle was based on a 30-min IV infusion of LNA-i-miR-221 on 4 consecutive days. Three patients within the first cohort were treated with 2 cycles (8 infusions), while 14 patients were treated with a single course (4 infusions); all patients were evaluated for phase 1 primary endpoint. The study was approved by the Ethics Committee and Regulatory Authorities (EudraCT 2017-002615-33).<br />Results: Seventeen patients received the investigational treatment, and 16 were evaluable for response. LNA-i-miR-221 was well tolerated, with no grade 3-4 toxicity, and the MTD was not reached. We recorded stable disease (SD) in 8 (50.0%) patients and partial response (PR) in 1 (6.3%) colorectal cancer case (total SD + PR: 56.3%). Pharmacokinetics indicated non-linear drug concentration increase across the dose range. Pharmacodynamics demonstrated concentration-dependent downregulation of miR-221 and upregulation of its CDKN1B/p27 and PTEN canonical targets. Five mg/kg was defined as the recommended phase II dose.<br />Conclusions: The excellent safety profile, the promising bio-modulator, and the anti-tumor activity offer the rationale for further clinical investigation of LNA-i-miR-221 (ClinTrials.Gov: NCT04811898).<br /> (© 2023. The Author(s).)

Details

Language :
English
ISSN :
1756-8722
Volume :
16
Issue :
1
Database :
MEDLINE
Journal :
Journal of hematology & oncology
Publication Type :
Academic Journal
Accession number :
37365583
Full Text :
https://doi.org/10.1186/s13045-023-01468-8