Primary chemoablation of low-grade upper tract urothelial carcinoma using UGN-101, a mitomycin-containing reverse thermal gel (OLYMPUS): an open-label, single-arm, phase 3 trial.


Journal

The Lancet. Oncology
ISSN: 1474-5488
Titre abrégé: Lancet Oncol
Pays: England
ID NLM: 100957246

Informations de publication

Date de publication:
06 2020
Historique:
received: 20 12 2019
revised: 20 02 2020
accepted: 21 02 2020
entrez: 8 7 2020
pubmed: 8 7 2020
medline: 21 7 2020
Statut: ppublish

Résumé

Most patients with low-grade upper tract urothelial cancer are treated by radical nephroureterectomy. We aimed to assess the safety and activity of a non-surgical treatment using instillation of UGN-101, a mitomycin-containing reverse thermal gel. In this open-label, single-arm, phase 3 trial, participants were recruited from 24 academic sites in the USA and Israel. Patients (aged ≥18 years) with primary or recurrent biopsy-proven, low-grade upper tract urothelial cancer (measuring 5-15 mm in maximum diameter) and an Eastern Cooperative Oncology Group performance status score of less than 3 (Karnofsky Performance Status score >40) were registered to receive six instillations of once-weekly UGN-101 (mitomycin 4 mg per mL; dosed according to volume of patient's renal pelvis and calyces, maximum 60 mg per instillation) via retrograde catheter to the renal pelvis and calyces. All patients had a planned primary disease evaluation 4-6 weeks after the completion of initial therapy, in which the primary outcome of complete response was assessed, defined as negative 3-month ureteroscopic evaluation, negative cytology, and negative for-cause biopsy. Activity (complete response, expected to occur in >15% of patients) and safety were assessed by the investigator in all patients who received at least one dose of UGN-101. Data presented are from the data cutoff on May 22, 2019. This study is registered with ClinicalTrials.gov, NCT02793128. Between April 6, 2017, and Nov 26, 2018, 71 (96%) of 74 enrolled patients received at least one dose of UGN-101. 42 (59%, 95% CI 47-71; p<0·0001) patients had a complete response at the primary disease evaluation visit. The median follow-up for patients with a complete response was 11·0 months (IQR 5·1-12·4). The most frequently reported all-cause adverse events were ureteric stenosis in 31 (44%) of 71 patients, urinary tract infection in 23 (32%), haematuria in 22 (31%), flank pain in 21 (30%), and nausea in 17 (24%). 19 (27%) of 71 patients had study drug-related or procedure-related serious adverse events. No deaths were regarded as related to treatment. Primary chemoablation of low-grade upper tract urothelial cancer with intracavitary UGN-101 results in clinically significant disease eradication and might offer a kidney-sparing treatment alternative for these patients. UroGen Pharma.

Sections du résumé

BACKGROUND
Most patients with low-grade upper tract urothelial cancer are treated by radical nephroureterectomy. We aimed to assess the safety and activity of a non-surgical treatment using instillation of UGN-101, a mitomycin-containing reverse thermal gel.
METHODS
In this open-label, single-arm, phase 3 trial, participants were recruited from 24 academic sites in the USA and Israel. Patients (aged ≥18 years) with primary or recurrent biopsy-proven, low-grade upper tract urothelial cancer (measuring 5-15 mm in maximum diameter) and an Eastern Cooperative Oncology Group performance status score of less than 3 (Karnofsky Performance Status score >40) were registered to receive six instillations of once-weekly UGN-101 (mitomycin 4 mg per mL; dosed according to volume of patient's renal pelvis and calyces, maximum 60 mg per instillation) via retrograde catheter to the renal pelvis and calyces. All patients had a planned primary disease evaluation 4-6 weeks after the completion of initial therapy, in which the primary outcome of complete response was assessed, defined as negative 3-month ureteroscopic evaluation, negative cytology, and negative for-cause biopsy. Activity (complete response, expected to occur in >15% of patients) and safety were assessed by the investigator in all patients who received at least one dose of UGN-101. Data presented are from the data cutoff on May 22, 2019. This study is registered with ClinicalTrials.gov, NCT02793128.
FINDINGS
Between April 6, 2017, and Nov 26, 2018, 71 (96%) of 74 enrolled patients received at least one dose of UGN-101. 42 (59%, 95% CI 47-71; p<0·0001) patients had a complete response at the primary disease evaluation visit. The median follow-up for patients with a complete response was 11·0 months (IQR 5·1-12·4). The most frequently reported all-cause adverse events were ureteric stenosis in 31 (44%) of 71 patients, urinary tract infection in 23 (32%), haematuria in 22 (31%), flank pain in 21 (30%), and nausea in 17 (24%). 19 (27%) of 71 patients had study drug-related or procedure-related serious adverse events. No deaths were regarded as related to treatment.
INTERPRETATION
Primary chemoablation of low-grade upper tract urothelial cancer with intracavitary UGN-101 results in clinically significant disease eradication and might offer a kidney-sparing treatment alternative for these patients.
FUNDING
UroGen Pharma.

Identifiants

pubmed: 32631491
pii: S1470-2045(20)30147-9
doi: 10.1016/S1470-2045(20)30147-9
pii:
doi:

Substances chimiques

Antibiotics, Antineoplastic 0
Drug Carriers 0
Hydrogels 0
Mitomycin 50SG953SK6

Banques de données

ClinicalTrials.gov
['NCT02793128']

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

776-785

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Nir Kleinmann (N)

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

Surena F Matin (SF)

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

Phillip M Pierorazio (PM)

Brady Urological Institute, Johns Hopkins University, Baltimore, MD, USA.

John L Gore (JL)

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

Ahmad Shabsigh (A)

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

Brian Hu (B)

Department of Urology, Loma Linda University, Loma Linda, CA, USA.

Karim Chamie (K)

Department of Urology, University of California Los Angeles, Los Angeles, CA, USA.

Guilherme Godoy (G)

Department of Urology, Baylor College of Medicine, Houston, TX, USA.

Scott Hubosky (S)

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

Marcelino Rivera (M)

Department of Urology, Mayo Clinic Health System, Rochester, MN, USA.

Michael O'Donnell (M)

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

Marcus Quek (M)

Department of Urology, Loyola University Medical Center, Maywood, IL, USA.

Jay D Raman (JD)

Division of Urology, Penn State Health Milton S Hershey Medical Center, Hershey, PA, USA.

John J Knoedler (JJ)

Division of Urology, Penn State Health Milton S Hershey Medical Center, Hershey, PA, USA.

Douglas Scherr (D)

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

Joshua Stern (J)

Department of Urology, Albert Einstein College of Medicine, Bronx, NY, USA.

Christopher Weight (C)

Department of Urology, University of Minnesota Health, Minneapolis, MN, USA.

Alon Weizer (A)

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

Michael Woods (M)

Department of Urology, Loyola University Medical Center, Maywood, IL, USA.

Hristos Kaimakliotis (H)

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

Angela B Smith (AB)

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

Jennifer Linehan (J)

Department of Urology, John Wayne Cancer Institute, Santa Monica, CA, USA.

Jonathan Coleman (J)

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

Mitchell R Humphreys (MR)

Department of Urology, Mayo Clinic Phoenix, Scottsdale, AZ, USA.

Raymond Pak (R)

Department of Urology, Mayo Clinic Jacksonville, Jacksonville, FL, USA.

David Lifshitz (D)

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

Michael Verni (M)

Urology Center of Las Vegas, Las Vegas, NV, USA.

Mehrad Adibi (M)

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

Mahul B Amin (MB)

Department of Pathology, University of Tennessee Health Science Center, Memphis, TN, USA.

Elyse Seltzer (E)

UroGen Pharma, New York, NY, USA.

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.

Mark Schoenberg (M)

Department of Urology, Albert Einstein College of Medicine, Bronx, NY, USA; UroGen Pharma, New York, NY, USA.

Seth P Lerner (SP)

Department of Urology, Baylor College of Medicine, Houston, TX, USA. Electronic address: slerner@bcm.edu.

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Classifications MeSH