Effect of Fecal Microbiota, Live-Jslm (REBYOTA [RBL]) on Health-Related Quality of Life in Patients With Recurrent Clostridioides difficile Infection: Results From the PUNCH CD3 Clinical Trial

Author:

Garey Kevin W1ORCID,Dubberke Erik R2,Guo Amy3,Harvey Adam4,Yang Min5,García-Horton Viviana6,Fillbrunn Mirko5,Wang Hongjue5,Tillotson Glenn S7,Bancke Lindy L4,Feuerstadt Paul89

Affiliation:

1. University of Houston , Houston, Texas , USA

2. Washington University , St Louis, Missouri , USA

3. Ferring Pharmaceuticals , Parsippany, New Jersey , USA

4. Rebiotix, a Ferring Company , Roseville, Minnesota , USA

5. Analysis Group Inc., Boston, Massachusetts , USA

6. Analysis Group, Inc., New York, New York , USA

7. GST Micro, North, Virginia , USA

8. Yale University School of Medicine , New Haven, Connecticut , USA

9. PACT-Gastroenterology Center , New Haven, Connecticut , USA

Abstract

Abstract Background Recurrence of Clostridioides difficile infection (rCDI) is common, prolonging disease morbidity and leading to poor quality of life. We evaluated disease-specific health-related quality of life (HRQL) in patients with rCDI treated with fecal microbiota, live-jslm (REBYOTA [RBL]; Rebiotix) versus placebo. Methods This was a secondary analysis of a randomized, double-blind, placebo-controlled phase 3 study (PUNCH CD3). The disease-specific Clostridioides difficile Quality of Life Survey (Cdiff32) was administered at baseline and at weeks 1, 4, and 8. Changes in Cdiff32 total and domain (physical, mental, social) scores from baseline to week 8 were compared between RBL and placebo and for responders and nonresponders. Results Findings were analyzed in a total of 185 patients (RBL, n = 128 [69.2%]; placebo, n = 57 [30.8%]) with available Cdiff32 data. Patients from both arms showed significant improvements in Cdiff32 scores relative to baseline across all outcomes and at all time points (all P < .001); RBL-treated patients showed significantly greater improvements in mental domain than those receiving placebo. In adjusted analyses, RBL-treated patients showed greater improvements than placebo in total score and physical and mental domains (all P < .05). Similar improvement in mental domain was observed among responders, while nonresponders showed numerical improvements with RBL but not placebo. Conclusions In a phase 3 double-blinded clinical trial, RBL-treated patients reported more substantial and sustained disease-specific HRQL improvements than placebo-treated patients. Clinical Trials Registration ClinicalTrials.gov NCT03244644 (https://clinicaltrials.gov/ct2/show/NCT03244644).

Funder

Ferring Pharmaceuticals

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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