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Primary results of STRONG: An open-label, multicenter, phase 3b study of fixed-dose durvalumab monotherapy in previously treated patients with urinary tract carcinoma

Authors
 Sonpavde, Guru P.  ;  Sternberg, Cora N.  ;  Loriot, Yohann  ;  Marabelle, Aurelien  ;  Lee, Jae Lyun  ;  Flechon, Aude  ;  Roubaud, Guilhem  ;  Pouessel, Damien  ;  Zagonel, Vittorina  ;  Calabro, Fabio  ;  Banna, Giuseppe L.  ;  Shin, Sang Joon  ;  Vera-Badillo, Francisco E.  ;  Powles, Thomas  ;  Hellmis, Eva  ;  Miranda, Paulo A. P.  ;  Lima, Ana Rita  ;  Emeribe, Ugochi  ;  Oh, Sun Min  ;  Hotte, Sebastien J. 
Citation
 European Journal of Cancer, Vol.163 : 55-65, 2022-03 
Journal Title
EUROPEAN JOURNAL OF CANCER
ISSN
 0959-8049 
Issue Date
2022-03
Keywords
Adverse events of special interest ; Durvalumab ; Fixed dose ; Immune checkpoint inhibitor ; Immune-mediated adverse events ; Immune-related adverse events ; Overall survival ; PD-L1 ; Urinary tract carcinoma ; Urothelial carcinoma
Abstract
Background: Prior durvalumab (anti-PD-L1 agent) studies in platinum-refractory metastatic urothelial carcinoma evaluated a dose of 10 mg/kg administered every two weeks. The nonrandomised phase 3b STRONG study (NCT03084471) evaluated the safety and efficacy of fixed-dose durvalumab at a more convenient dosing schedule in a previously treated patient population, more similar to a real-world clinical setting.Patients and methods: 867 patients with urothelial or nonurothelial urinary tract carcinoma (UTC) who progressed on or after platinum or nonplatinum chemotherapy were treated with durvalumab 1500 mg every four weeks; 87% had an Eastern Cooperative Oncology Group performance status (ECOG PS) of 0-1, and 13% had an ECOG PS of 2. The primary endpoint was the incidence of adverse events of special interest (AESIs), including immune mediated AEs (imAEs). Secondary and exploratory end-points included overall survival (OS), objective response rate (ORR) and disease control rate (at six and 12 months) (DCR).Results: AESIs of any grade were reported in 51% of patients (8% grade > 3). The incidence of imAEs was 11% (2% grade > 3). The median OS was 7.0 months (95% confidence interval [CI]: 6.4-8.2) and ORR was 18% (95% CI: 14.8-20.6), with complete responses in 5% of patients and a DCR at six months of 19% (95% CI: 16.1-22.1). Conclusion: Fixed-dose durvalumab monotherapy every four weeks has an acceptable safety profile and yields durable clinical activity in previously chemotherapy-treated patients with UTC. Safety and efficacy are consistent with previous durvalumab studies and other antiPD-1/PD-L1 agents in this setting.Clinicaltrials.gov identifier: NCT03084471 https://clinicaltrials.gov/ct2/show/NCT03084471. 2021 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
DOI
10.1016/j.ejca.2021.12.012
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Shin, Sang Joon(신상준) ORCID logo https://orcid.org/0000-0001-5350-7241
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/193476
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