Durability of Response to Primary Chemoablation of Low-Grade Upper Tract Urothelial Carcinoma Using UGN-101, a Mitomycin-Containing Reverse Thermal Gel: OLYMPUS Trial Final Report.


Journal

The Journal of urology
ISSN: 1527-3792
Titre abrégé: J Urol
Pays: United States
ID NLM: 0376374

Informations de publication

Date de publication:
Apr 2022
Historique:
pubmed: 18 12 2021
medline: 16 3 2022
entrez: 17 12 2021
Statut: ppublish

Résumé

Our goal was to evaluate long-term safety and durability of response to UGN-101, a mitomycin-containing reverse thermal gel, as primary chemoablative treatment for low-grade upper tract urothelial carcinoma. In this open-label, single-arm, multicenter, phase 3 trial (NCT02793128), patients ≥18 years of age with primary or recurrent biopsy-proven low-grade upper tract urothelial carcinoma received 6 once-weekly instillations of UGN-101 via retrograde catheter to the renal pelvis and calyces. Those with complete response (defined as negative ureteroscopic evaluation, negative cytology and negative for-cause biopsy) 4-6 weeks after the last instillation were eligible for up to 11 monthly maintenance instillations and were followed for ≥12 months with quarterly evaluation of response durability. Durability of complete response was determined by ureteroscopic evaluation; duration of response was estimated by the Kaplan-Meier method. Treatment-emergent adverse events (TEAEs) were monitored. Of 71 patients who initiated treatment, 41 (58%) had complete response to induction therapy and consented to long-term followup; 23/41 patients (56%) remained in complete response after 12 months (95% CI 40, 72), comprising 6/12 (50%) who did not receive any maintenance instillations and 17/29 (59%) who received ≥1 maintenance instillation. Kaplan-Meier analysis of durability was estimated as 82% (95% CI 66, 91) at 12 months. Ureteric stenosis was the most frequently reported TEAE (31/71, 44%); an increasing number of instillations appeared to be associated with increased incidence of urinary TEAEs. Durability of response to UGN-101 with or without maintenance treatment is clinically meaningful, offering a kidney-sparing therapeutic alternative for patients with low-grade disease.

Identifiants

pubmed: 34915741
doi: 10.1097/JU.0000000000002350
doi:

Substances chimiques

Antibiotics, Antineoplastic 0
Hydrogels 0
Mitomycin 50SG953SK6

Types de publication

Clinical Trial, Phase III Controlled Clinical Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

779-788

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Surena F Matin (SF)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Phillip M Pierorazio (PM)

Brady Urological Institute, The Johns Hopkins University, Baltimore, Maryland.

Nir Kleinmann (N)

Department of Urology, Sheba Medical Center, Ramat Gan, Israel.

John L Gore (JL)

Department of Urology, University of Washington Medical Center, Seattle, Washington.

Ahmad Shabsigh (A)

Department of Urology, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.

Brian Hu (B)

Department of Urology, Loma Linda University, Loma Linda, California.

Karim Chamie (K)

Department of Urology, UCLA, Los Angeles, California.

Guilherme Godoy (G)

Scott Department of Urology, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas.

Scott G Hubosky (SG)

Department of Urology, Sidney Kimmel Medical College at Thomas Jefferson University Hospitals, Philadelphia, Pennsylvania.

Marcelino Rivera (M)

Department of Urology, Mayo Clinic Health System, Rochester, Minnesota.

Michael O'Donnell (M)

Department of Urology, University of Iowa, Iowa City, Iowa.

Marcus Quek (M)

Department of Urology, Loyola University Medical Center, Maywood, Illinois.

Jay D Raman (JD)

Division of Urology, Pennsylvania State Health Milton S. Hershey Medical Center, Hershey, Pennsylvania.

John J Knoedler (JJ)

Division of Urology, Pennsylvania State Health Milton S. Hershey Medical Center, Hershey, Pennsylvania.

Douglas Scherr (D)

Department of Urology, Weill Medical College of Cornell University, New York, New York.

Christopher Weight (C)

Cleveland Clinic, Glickman Urological and Kidney Institute, Cleveland, Ohio.

Alon Weizer (A)

Department of Urology, University of Michigan, Ann Arbor, Michigan.

Michael Woods (M)

Department of Urology, Loyola University Medical Center, Maywood, Illinois.

Hristos Kaimakliotis (H)

Department of Urology, Indiana University School of Medicine, Indianapolis, Indiana.

Angela B Smith (AB)

Department of Urology, University of North Carolina School of Medicine, Chapel Hill, North Carolina.

Jennifer Linehan (J)

Department of Urology, John Wayne Cancer Institute, Santa Monica, California.

Jonathan Coleman (J)

Department of Urology, Memorial Sloan-Kettering Cancer Center, New York, New York.

Mitchell R Humphreys (MR)

Department of Urology, Mayo Clinic-Phoenix, Scottsdale, Arizona.

Raymond Pak (R)

Department of Urology, Mayo Clinic-Jacksonville, Jacksonville, Florida.

David Lifshitz (D)

Department of Urology, Rabin Medical Center, Tel Aviv, Israel.

Michael Verni (M)

Urology Center of Las Vegas, Las Vegas, Nevada.

Ifat Klein (I)

UroGen Pharma, Ra'anana, Israel.

Marina Konorty (M)

UroGen Pharma, Ra'anana, Israel.

Dalit Strauss-Ayali (D)

UroGen Pharma, Ra'anana, Israel.

Gil Hakim (G)

UroGen Pharma, Ra'anana, Israel.

Elyse Seltzer (E)

UroGen Pharma, Princeton, New Jersey.

Mark Schoenberg (M)

UroGen Pharma, Princeton, New Jersey.
Department of Urology, Albert Einstein College of Medicine, Bronx, New York.

Seth P Lerner (SP)

Scott Department of Urology, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas.

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Classifications MeSH