Phase 1 study of MRX34, a liposomal miR-34a mimic, in patients with advanced solid tumours

David S. Hong(The University of Texas MD Anderson Cancer Center), Yoon‐Koo Kang(Asan Medical Center), Mitesh J. Borad(Mayo Clinic in Arizona), Jasgit C. Sachdev(Scottsdale Research Institute (United States)), Samuel Ejadi(University of California, Irvine Medical Center), Ho Yeong Lim(Samsung Medical Center), Andrew Brenner(The University of Texas at San Antonio Health Science Center), Keunchil Park(Samsung Medical Center), Jae‐Lyun Lee(Asan Medical Center), Tae‐You Kim(Seoul National University Hospital), SangJoon Shin(Severance Hospital), Carlos Becerra(Texas Oncology), Gerald S. Falchook(Sarah Cannon), Jay Stoudemire(Mirna Therapeutics (United States)), Desiree Martin(Mirna Therapeutics (United States)), Kevin Kelnar(Mirna Therapeutics (United States)), Heidi J. Peltier(Mirna Therapeutics (United States)), Vinícius Bonato(Mirna Therapeutics (United States)), Andreas G. Bader(Mirna Therapeutics (United States)), Susan Smith(Mirna Therapeutics (United States)), Sinil Kim(Mirna Therapeutics (United States)), Vincent O’Neill(Mirna Therapeutics (United States)), Muhammad Shaalan Beg(The University of Texas Southwestern Medical Center)
British Journal of Cancer
April 1, 2020
Cited by 900Open Access
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Abstract

BACKGROUND: In this first-in-human, Phase 1 study of a microRNA-based cancer therapy, the recommended Phase 2 dose (RP2D) of MRX34, a liposomal mimic of microRNA-34a (miR-34a), was determined and evaluated in patients with advanced solid tumours. METHODS: Adults with various solid tumours refractory to standard treatments were enrolled in 3 + 3 dose-escalation cohorts and, following RP2D determination, expansion cohorts. MRX34, with oral dexamethasone premedication, was given intravenously daily for 5 days in 3-week cycles. RESULTS: for non-HCC cancers. Pharmacodynamic results showed delivery of miR-34a to tumours, and dose-dependent modulation of target gene expression in white blood cells. Three patients had PRs and 16 had SD lasting ≥4 cycles (median, 19 weeks, range, 11-55). CONCLUSION: MRX34 treatment with dexamethasone premedication demonstrated a manageable toxicity profile in most patients and some clinical activity. Although the trial was closed early due to serious immune-mediated AEs that resulted in four patient deaths, dose-dependent modulation of relevant target genes provides proof-of-concept for miRNA-based cancer therapy. CLINICAL TRIAL REGISTRATION: NCT01829971.


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