Efficacy and Health-Related Quality of Life Impact of Fecal Microbiota, Live-js']jslm: A Post Hoc Analysis of PUNCH CD3 Patients at First Recurrence of Clostridioides difficile Infection

被引:5
作者
Feuerstadt, Paul [1 ,2 ]
Allegretti, Jessica R. [3 ]
Dubberke, Erik R. [4 ]
Guo, Amy [5 ]
Harvey, Adam [6 ]
Yang, Min [7 ,8 ]
Garcia-Horton, Viviana [9 ]
Fillbrunn, Mirko [7 ]
Tillotson, Glenn [10 ]
Bancke, Lindy L. [6 ]
LaPlante, Kerry [11 ,12 ]
Garey, Kevin W. [13 ]
Khanna, Sahil [14 ]
机构
[1] Yale Univ, Sch Med, New Haven, CT 06520 USA
[2] PACT Gastroenterol Ctr, 2200 Whitney Ave Suite 330 & 360, Hamden, CT 06518 USA
[3] Brigham & Womens Hosp, Boston, MA USA
[4] Washington Univ, St Louis, MO USA
[5] Ferring Pharmaceut Inc, Parsippany, NJ USA
[6] Ferring Co, Rebiotix, Roseville, MN USA
[7] Anal Grp Inc, Boston, MA USA
[8] Univ Texas Austin, Austin, TX USA
[9] Anal Grp Inc, New York, NY USA
[10] GST Micro LLC, North, VA USA
[11] Univ Rhode Isl, Kingston, RI USA
[12] Brown Univ, Warren Alpert Med Sch, Providence, RI USA
[13] Univ Houston, Houston, TX USA
[14] Mayo Clin, Rochester, MN USA
关键词
REBYOTA; PUNCH CD3; Clostridioides difficile infection; Health-related quality of life; Treatment efficacy; UPDATE; RISK;
D O I
10.1007/s40121-023-00907-w
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction Clostridioides difficile infection (CDI) causes symptoms of varying severity and negatively impacts patients' health-related quality of life (HRQL). Despite antibiotic treatment, recurrence of CDI (rCDI) is common and imposes clinical and economic burdens on patients. Fecal microbiota, live-jslm (REBYOTA [RBL]) is newly approved in the USA for prevention of rCDI following antibiotic treatments. We analyzed efficacy and HRQL impact of RBL vs. placebo in patients at first rCDI using data from the phase 3 randomized, double-blind placebo-controlled clinical trial, PUNCH CD3.Methods This post hoc analysis included patients at first rCDI fromPUNCH CD3. Treatment success (i.e., absence of diarrhea within 8 weeks post-treatment) was analyzed adjusting for baseline patient characteristics. HRQL was measured using the Clostridioides difficile Quality of Life Survey (Cdiff32); absolute scores and change from baseline in total and domain (physical, mental, and social) scores were summarized and compared between arms. Analyses were conducted for the trial's blinded phase only.Results Among 86 eligible patients (32.8% of the overall trial population, RBL 53 [61.6%], placebo 33 [38.4%]), RBL-treated patients had significantly lower odds of recurrence (i.e., greater probability of treatment success) at week 8 vs. placebo (odds ratio 0.35 [95% confidence interval 0.13, 0.98]). Probability of treatment success at week 8 was 81% for RBL and 60% for placebo, representing 21% absolute and 35% relative increases for RBL (crude proportions 79.2% vs. 60.6%; relative risk 0.53, p = 0.06). Additionally, RBL was associated with significantly higher Cdiff32 total (change score difference 13.5 [standard deviation 5.7], p < 0.05) and mental domain (16.2 [6.0], p < 0.01) scores vs. placebo from baseline to week 8.Conclusion Compared to placebo, RBL demonstrated a significantly higher treatment success in preventing further rCDI and enhanced HRQL among patients at first recurrence, establishing RBL as an effective treatment to prevent further recurrences in these patients.Trial RegistrationClinicalTrials.gov Identifier NCT03244644.
引用
收藏
页码:221 / 236
页数:16
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