» Articles » PMID: 37185390

Systematic Literature Review (SLR) and Network Meta-Analysis (NMA) of First-Line Therapies (1L) for Locally Advanced/Metastatic Urothelial Carcinoma (la/mUC)

Overview
Journal Curr Oncol
Publisher MDPI
Specialty Oncology
Date 2023 May 15
PMID 37185390
Authors
Affiliations
Soon will be listed here.
Abstract

To compare efficacy outcomes for all approved and investigational first-line (1L) treatment regimens for locally advanced or metastatic urothelial carcinoma (la/mUC) with standard of care (SOC), a network meta-analysis (NMA) was conducted. A systematic literature review (SLR) identified phase 2 and 3 randomized trials investigating 1L treatment regimens in la/mUC published January 2001-September 2021. Three networks were formed based on cisplatin (cis) eligibility: cis-eligible/mixed (cis-eligible patients and mixed populations of cis-eligible/ineligible patients), cis-ineligible (strict; exclusively cis-ineligible patients), and cis-ineligible (wide; including studies with investigator's choice of carbo). Analyses examined comparative efficacy by hazard ratio (HR) for overall survival (OS), and progression-free survival (PFS), and odds ratio (OR) for overall response rate (ORR), with 1L regimens vs. SOC. SOC was gemcitabine + cis (GemCis) or carboplatin (GemCarbo), cis-eligible/mixed network, and GemCarbo cis-ineligible networks. Of 1906 SLR identified citations, 55 trials were selected for data extraction. The NMA comprised 11, 6, and 8 studies in the cis-eligible/mixed, cis-ineligible (strict), cis-ineligible (wide) networks, respectively. In a meta-analysis of SOC control arms, median (95% CI) overall survival (OS) in months varied by network: 13.19 (12.43, 13.95) cis-eligible/mixed, 11.96 (10.43, 13.48) cis-ineligible (wide), and 9.74 (6.71, 12.76) cis-ineligible (strict). Most differences in OS, PFS, and ORR with treatment regimens across treatment networks were not statistically significant compared with SOC. Outcomes with current 1L regimens remain poor, and few significant improvements over SOC have been made, despite inclusion of recent clinical trial data, highlighting an unmet need in the la/mUC patient population.

Citing Articles

Epidemiology, resource use, and treatment patterns of locally advanced or metastatic urothelial carcinoma in France.

Joly F, Culine S, Roupret M, Tricotel A, Casarotto E, Brice S Future Oncol. 2025; 21(6):665-679.

PMID: 39973175 PMC: 11881851. DOI: 10.1080/14796694.2025.2459058.


Phase 2 Trial of Enfortumab Vedotin in Patients With Previously Treated Locally Advanced or Metastatic Urothelial Carcinoma in China.

Li S, Shi Y, Dong H, Guo H, Xie Y, Sun Z Cancer Med. 2024; 13(21):e70368.

PMID: 39530574 PMC: 11555717. DOI: 10.1002/cam4.70368.


Patient Preferences for First-Line Treatment of Locally Advanced or Metastatic Urothelial Carcinoma: An Application of Multidimensional Thresholding.

Apolo A, Michaels-Igbokwe C, Simon N, Benjamin D, Farrar M, Hepp Z Patient. 2024; 18(1):77-87.

PMID: 39198374 PMC: 11717873. DOI: 10.1007/s40271-024-00709-3.


Real-world treatment patterns and quality of life among patients with locally advanced or metastatic urothelial carcinoma living in Saudi Arabia, South Korea, Taiwan, and Turkey.

Cheng L, Kim J, Mukherjee A, Milloy N, Unsworth M, Ng D Int J Urol. 2024; 31(8):933-943.

PMID: 38787505 PMC: 11524135. DOI: 10.1111/iju.15497.


Real-world epidemiology and treatment patterns of patients with locally advanced or metastatic urothelial carcinoma: Retrospective analysis of Diagnosis Procedure Combination claims data in Japan.

Asakawa K, Waratani M, Massey O, Holbrook T, Kondo M, Saito A Int J Urol. 2024; 31(7):730-738.

PMID: 38468564 PMC: 11524106. DOI: 10.1111/iju.15450.


References
1.
Powles T, van der Heijden M, Castellano D, Galsky M, Loriot Y, Petrylak D . Durvalumab alone and durvalumab plus tremelimumab versus chemotherapy in previously untreated patients with unresectable, locally advanced or metastatic urothelial carcinoma (DANUBE): a randomised, open-label, multicentre, phase 3 trial. Lancet Oncol. 2020; 21(12):1574-1588. DOI: 10.1016/S1470-2045(20)30541-6. View

2.
Hoaglin D, Hawkins N, Jansen J, Scott D, Itzler R, Cappelleri J . Conducting indirect-treatment-comparison and network-meta-analysis studies: report of the ISPOR Task Force on Indirect Treatment Comparisons Good Research Practices: part 2. Value Health. 2011; 14(4):429-37. DOI: 10.1016/j.jval.2011.01.011. View

3.
Lorusso V, Crucitta E, Silvestris N, Rosati G, Manzione L, De Lena M . Randomised, open-label, phase II trial of paclitaxel, gemcitabine and cisplatin versus gemcitabine and cisplatin as first-line chemotherapy in advanced transitional cell carcinoma of the urothelium. Oncol Rep. 2005; 13(2):283-7. View

4.
Holmsten K, Jensen N, Mouritsen L, Jonsson E, Mellnert C, Agerbaek M . Vinflunine/gemcitabine versus carboplatin/gemcitabine as first-line treatment in cisplatin-ineligible patients with advanced urothelial carcinoma: A randomised phase II trial (VINGEM). Eur J Cancer. 2019; 127:173-182. DOI: 10.1016/j.ejca.2019.08.033. View

5.
Bamias A, Dafni U, Karadimou A, Timotheadou E, Aravantinos G, Psyrri A . Prospective, open-label, randomized, phase III study of two dose-dense regimens MVAC versus gemcitabine/cisplatin in patients with inoperable, metastatic or relapsed urothelial cancer: a Hellenic Cooperative Oncology Group study (HE 16/03). Ann Oncol. 2012; 24(4):1011-7. DOI: 10.1093/annonc/mds583. View