Refractory Pseudomonas aeruginosa infections treated with phage PASA16: A compassionate use case series

系列(地层学) 耐火材料(行星科学) 同情性使用 临床试验 医学 铜绿假单胞菌 内科学 微生物学 生物 细菌 天体生物学 遗传学 古生物学
作者
Hadil Onallah,Ronen Hazan,Ran Nir‐Paz,Michael Brownstein,Joseph Fackler,Bri’Anna Horne,Robert E. Hopkins,Subhendu Basu,Ortal Yerushalmy,Sivan Alkalay‐Oren,Ron Braunstein,Amit Rimon,Daniel Gelman,Leron Khalifa,Karen Adler,Mohanad Abdalrhman,Shira Gelman,Eyal Katvan,Shunit Coppenhagen‐Glazer,Allon E. Moses
出处
期刊:Med [Elsevier BV]
卷期号:4 (9): 600-611.e4 被引量:35
标识
DOI:10.1016/j.medj.2023.07.002
摘要

A growing number of compassionate phage therapy cases were reported in the last decade, with a limited number of clinical trials conducted and few unsuccessful clinical trials reported. There is only a little evidence on the role of phages in refractory infections. Our objective here was to present the largest compassionate-use single-organism/phage case series in 16 patients with non-resolving Pseudomonas aeruginosa infections.We summarized clinical phage microbiology susceptibility data, administration protocol, clinical data, and outcomes of all cases treated with PASA16 phage. In all intravenous phage administrations, PASA16 phage was manufactured and provided pro bono by Adaptive Phage Therapeutics. PASA16 was administered intravenously, locally to infection site, or by topical use to 16 patients, with data available for 15 patients, mainly with osteoarticular and foreign-device-associated infections.A few minor side effects were noted, including elevated liver function enzymes and a transient reduction in white blood cell count. Good clinical outcome was documented in 13 out of 15 patients (86.6%). Two clinical failures were reported. The minimum therapy duration was 8 days with a once- to twice-daily regimen.PASA16 with antibiotics was found to be relatively successful in patients for whom traditional treatment approaches have failed previously. Such pre-phase-1 cohorts can outline potential clinical protocols and facilitate the design of future trials.The study was funded in part by The Israeli Science Foundation IPMP (ISF_1349/20), Rosetrees Trust (A2232), United States-Israel Binational Science Foundation (2017123), and the Milgrom Family Support Program.
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