One-Year Results for the ROBUST III Randomized Controlled Trial Evaluating the Optilume ® Drug-Coated Balloon for Anterior Urethral Strictures

The Optilume® drug-coated balloon (DCB) is a urethral dilation balloon with a paclitaxel coating that combines mechanical dilation for immediate symptomatic relief with local drug delivery to maintain urethral patency. The ROBUST III study is a randomized, single-blind trial evaluating the safety an...

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Veröffentlicht in:The Journal of urology Jg. 207; H. 4; S. 866
Hauptverfasser: Elliott, Sean P, Coutinho, Karl, Robertson, Kaiser J, D'Anna, Richard, Chevli, Kent, Carrier, Serge, Aube-Peterkin, Melanie, Cantrill, Christopher H, Ehlert, Michael J, Te, Alexis E, Dann, Jeffrey, DeLong, Jessica M, Brandes, Steven B, Hagedorn, Judith C, Levin, Richard, Schlaifer, Amy, DeSouza, Euclid, DiMarco, David, Erickson, Brad A, Natale, Richard, Husmann, Douglas A, Morey, Allen, Olsson, Carl, Virasoro, Ramón
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States 01.04.2022
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ISSN:1527-3792, 1527-3792
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Abstract The Optilume® drug-coated balloon (DCB) is a urethral dilation balloon with a paclitaxel coating that combines mechanical dilation for immediate symptomatic relief with local drug delivery to maintain urethral patency. The ROBUST III study is a randomized, single-blind trial evaluating the safety and efficacy of the Optilume DCB against endoscopic management of recurrent anterior urethral strictures. Eligible patients were adult males with anterior strictures ≤12Fr in diameter and ≤3 cm in length, at least 2 prior endoscopic treatments, International Prostate Symptom Score ≥11 and maximum flow rate <15 ml per second. A total of 127 subjects were enrolled at 22 sites. The primary study end point was anatomical success (≥14Fr by cystoscopy or calibration) at 6 months. Key secondary end points included freedom from repeat treatment, International Prostatic Symptom Score and peak flow rate. The primary safety end point included freedom from serious device- or procedure-related complications. Baseline characteristics were similar between groups, with subjects having an average of 3.6 prior treatments and average length of 1.7 cm. Anatomical success for Optilume DCB was significantly higher than control at 6 months (75% vs 27%, p <0.001). Freedom from repeat intervention was significantly higher in the Optilume DCB arm. Immediate symptom and urinary flow rate improvement was significant in both groups, with the benefit being more durable in the Optilume DCB group. The most frequent adverse events included urinary tract infection, post-procedural hematuria and dysuria. The results of this randomized controlled trial support that Optilume is safe and superior to standard direct vision internal urethrotomy/dilation for the treatment of recurrent anterior urethral strictures <3 cm in length. The Optilume DCB may serve as an important alternative for men who have had an unsuccessful direct vision internal urethrotomy/dilation but want to avoid or delay urethroplasty.
AbstractList The Optilume® drug-coated balloon (DCB) is a urethral dilation balloon with a paclitaxel coating that combines mechanical dilation for immediate symptomatic relief with local drug delivery to maintain urethral patency. The ROBUST III study is a randomized, single-blind trial evaluating the safety and efficacy of the Optilume DCB against endoscopic management of recurrent anterior urethral strictures.PURPOSEThe Optilume® drug-coated balloon (DCB) is a urethral dilation balloon with a paclitaxel coating that combines mechanical dilation for immediate symptomatic relief with local drug delivery to maintain urethral patency. The ROBUST III study is a randomized, single-blind trial evaluating the safety and efficacy of the Optilume DCB against endoscopic management of recurrent anterior urethral strictures.Eligible patients were adult males with anterior strictures ≤12Fr in diameter and ≤3 cm in length, at least 2 prior endoscopic treatments, International Prostate Symptom Score ≥11 and maximum flow rate <15 ml per second. A total of 127 subjects were enrolled at 22 sites. The primary study end point was anatomical success (≥14Fr by cystoscopy or calibration) at 6 months. Key secondary end points included freedom from repeat treatment, International Prostatic Symptom Score and peak flow rate. The primary safety end point included freedom from serious device- or procedure-related complications.MATERIALS AND METHODSEligible patients were adult males with anterior strictures ≤12Fr in diameter and ≤3 cm in length, at least 2 prior endoscopic treatments, International Prostate Symptom Score ≥11 and maximum flow rate <15 ml per second. A total of 127 subjects were enrolled at 22 sites. The primary study end point was anatomical success (≥14Fr by cystoscopy or calibration) at 6 months. Key secondary end points included freedom from repeat treatment, International Prostatic Symptom Score and peak flow rate. The primary safety end point included freedom from serious device- or procedure-related complications.Baseline characteristics were similar between groups, with subjects having an average of 3.6 prior treatments and average length of 1.7 cm. Anatomical success for Optilume DCB was significantly higher than control at 6 months (75% vs 27%, p <0.001). Freedom from repeat intervention was significantly higher in the Optilume DCB arm. Immediate symptom and urinary flow rate improvement was significant in both groups, with the benefit being more durable in the Optilume DCB group. The most frequent adverse events included urinary tract infection, post-procedural hematuria and dysuria.RESULTSBaseline characteristics were similar between groups, with subjects having an average of 3.6 prior treatments and average length of 1.7 cm. Anatomical success for Optilume DCB was significantly higher than control at 6 months (75% vs 27%, p <0.001). Freedom from repeat intervention was significantly higher in the Optilume DCB arm. Immediate symptom and urinary flow rate improvement was significant in both groups, with the benefit being more durable in the Optilume DCB group. The most frequent adverse events included urinary tract infection, post-procedural hematuria and dysuria.The results of this randomized controlled trial support that Optilume is safe and superior to standard direct vision internal urethrotomy/dilation for the treatment of recurrent anterior urethral strictures <3 cm in length. The Optilume DCB may serve as an important alternative for men who have had an unsuccessful direct vision internal urethrotomy/dilation but want to avoid or delay urethroplasty.CONCLUSIONSThe results of this randomized controlled trial support that Optilume is safe and superior to standard direct vision internal urethrotomy/dilation for the treatment of recurrent anterior urethral strictures <3 cm in length. The Optilume DCB may serve as an important alternative for men who have had an unsuccessful direct vision internal urethrotomy/dilation but want to avoid or delay urethroplasty.
The Optilume® drug-coated balloon (DCB) is a urethral dilation balloon with a paclitaxel coating that combines mechanical dilation for immediate symptomatic relief with local drug delivery to maintain urethral patency. The ROBUST III study is a randomized, single-blind trial evaluating the safety and efficacy of the Optilume DCB against endoscopic management of recurrent anterior urethral strictures. Eligible patients were adult males with anterior strictures ≤12Fr in diameter and ≤3 cm in length, at least 2 prior endoscopic treatments, International Prostate Symptom Score ≥11 and maximum flow rate <15 ml per second. A total of 127 subjects were enrolled at 22 sites. The primary study end point was anatomical success (≥14Fr by cystoscopy or calibration) at 6 months. Key secondary end points included freedom from repeat treatment, International Prostatic Symptom Score and peak flow rate. The primary safety end point included freedom from serious device- or procedure-related complications. Baseline characteristics were similar between groups, with subjects having an average of 3.6 prior treatments and average length of 1.7 cm. Anatomical success for Optilume DCB was significantly higher than control at 6 months (75% vs 27%, p <0.001). Freedom from repeat intervention was significantly higher in the Optilume DCB arm. Immediate symptom and urinary flow rate improvement was significant in both groups, with the benefit being more durable in the Optilume DCB group. The most frequent adverse events included urinary tract infection, post-procedural hematuria and dysuria. The results of this randomized controlled trial support that Optilume is safe and superior to standard direct vision internal urethrotomy/dilation for the treatment of recurrent anterior urethral strictures <3 cm in length. The Optilume DCB may serve as an important alternative for men who have had an unsuccessful direct vision internal urethrotomy/dilation but want to avoid or delay urethroplasty.
Author Hagedorn, Judith C
Erickson, Brad A
Husmann, Douglas A
Coutinho, Karl
Carrier, Serge
Elliott, Sean P
Cantrill, Christopher H
Robertson, Kaiser J
Virasoro, Ramón
DeSouza, Euclid
Chevli, Kent
DeLong, Jessica M
Schlaifer, Amy
Natale, Richard
Ehlert, Michael J
Te, Alexis E
Dann, Jeffrey
Olsson, Carl
D'Anna, Richard
Aube-Peterkin, Melanie
Brandes, Steven B
Morey, Allen
Levin, Richard
DiMarco, David
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  organization: University of Minnesota, Minneapolis, Minnesota
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  organization: New Jersey Urology LLC, Millburn, New Jersey
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  organization: Chesapeake Urology, Hanover, Maryland
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  organization: Arkansas Urology, Little Rock, Arkansas
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  organization: Western New York Urology Associates, Cheektowaga, New York
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  organization: McGill University Health Center, Montreal, Quebec, Canada
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  organization: Urology San Antonio, San Antonio, Texas
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  organization: Metro Urology, a division of Minnesota Urology, Woodbury, Minnesota
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  organization: Weill Cornell Medicine, New York, New York
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  organization: Advanced Urology Institute, Daytona Beach, Florida
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  surname: DeLong
  fullname: DeLong, Jessica M
  organization: Urology of Virginia PLLC, Virginia Beach, Virginia
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  givenname: Steven B
  surname: Brandes
  fullname: Brandes, Steven B
  organization: Columbia University, New York, New York
– sequence: 14
  givenname: Judith C
  surname: Hagedorn
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  organization: University of Washington, Seattle, Washington
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  givenname: Richard
  surname: Levin
  fullname: Levin, Richard
  organization: Chesapeake Urology Research Associates, Annapolis, Maryland
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  organization: Academic Urology & Urogynecology of Arizona, Phoenix, Arizona
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  organization: Adult and Pediatric Urology PC, Omaha, Nebraska
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  organization: Oregon Urology Institute, Springfield, Oregon
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  surname: Erickson
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  organization: University of Iowa Hospitals and Clinics, Iowa City, Iowa
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  surname: Natale
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  organization: Carolina Urology Partners PLLC, Concord, North Carolina
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  givenname: Douglas A
  surname: Husmann
  fullname: Husmann, Douglas A
  organization: Mayo Clinic, Rochester, Minnesota
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  givenname: Allen
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  fullname: Morey, Allen
  organization: UT Southwestern Medical Center, Dallas, Texas
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  givenname: Carl
  surname: Olsson
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  organization: Integrated Medical Professionals, New York, New York
– sequence: 24
  givenname: Ramón
  surname: Virasoro
  fullname: Virasoro, Ramón
  organization: Urology of Virginia PLLC, Virginia Beach, Virginia
BackLink https://www.ncbi.nlm.nih.gov/pubmed/34854748$$D View this record in MEDLINE/PubMed
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lower urinary tract symptoms
urinary bladder neck obstruction
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References 35014865 - J Urol. 2022 Apr;207(4):941-942
34963296 - J Urol. 2022 Apr;207(4):874-875
34963297 - J Urol. 2022 Apr;207(4):874
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Snippet The Optilume® drug-coated balloon (DCB) is a urethral dilation balloon with a paclitaxel coating that combines mechanical dilation for immediate symptomatic...
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SubjectTerms Adult
Coated Materials, Biocompatible
Dilatation - adverse effects
Dilatation - methods
Humans
Male
Middle Aged
Paclitaxel - administration & dosage
Prospective Studies
Recurrence
Single-Blind Method
Treatment Outcome
Urethral Stricture - surgery
Title One-Year Results for the ROBUST III Randomized Controlled Trial Evaluating the Optilume ® Drug-Coated Balloon for Anterior Urethral Strictures
URI https://www.ncbi.nlm.nih.gov/pubmed/34854748
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