A meta-analysis assessing objective response rates with first-line systemic treatment options in locally advanced/metastatic urothelial carcinoma.

Authors

null

Akshat Saxena

Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ

Akshat Saxena , Syed Arsalan Ahmed Naqvi , Nikita Tripathi , Muhammad Ali Khan , Arifa Bibi , Tara Ballouz , Haidar Abdul-Muhsin , Mark Tyson , Irbaz Bin Riaz , Alan Haruo Bryce , Parminder Singh

Organizations

Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, Division of Hematology and Medical Oncology, Mayo Clinic, Phoenix, AZ, Division of Hematology and Medical Oncology, Mayo Clinic, Phoeniz, AZ, Division of Hematology and Oncology, Mayo Clinic, Phoenix, AZ, Department of Internal Medicine, Mayo Clinic, Scottsdale, AZ, Mayo Clinic Arizona, Phoenix, AZ, Division of Hematology and Oncology, Mayo Clinic, Scottsdale, AZ, Mayo Clinic Arizona, Scottsdale, AZ, Mayo Clinic, Phoenix, AZ

Research Funding

No funding sources reported

Background: Immunotherapy combined with chemotherapy (IO/C) as the first-line management of locally advanced or metastatic urothelial carcinoma (LA/mUC) has been investigated in multiple trials with conflicting outcomes. Therefore, we conducted a meta-analysis of available trials to compare objective response rates (ORR) of this combination regimen, both in overall and in cisplatin-ineligible populations. Methods: EMABSE and MEDLINE were searched from 2000 through July 20th, 2023, to identify phase II and III clinical trials assessing IO, C or both in LA/mUC. Main outcome of interest was objective response rates (ORR) as defined in the included trials. An inverse variance random-effects meta-analysis was performed to estimate pooled ORR using the restricted maximum likelihood estimation method. Subgroup differences were assessed among IO/C, IO alone, and C alone. The threshold for statistical significance was established at 0.1. Results: Of 5975 citations identified, a total of 26 trials with a total of 4,628 participants were included in this systematic review. In the overall group, the ORR in IO/C trials (5 trials, 1,236 patients) was 44.70% (95% CI: 21.88%- 70.0%). In IO trials (7 trials, 2,189 patients), ORR was 23.68% (19.55%- 28.36%) and in C trials (26 trials, 4,628 patients) was 43.46% (37.43%-49.68%]). In the cisplatin-ineligible group, the ORR in IO/C trials (2 trials, 240 patients) was 60.06% (33.38%-81.86%), in IO trials (6 trials, 1,103 patients) was 26.15% (23.01%; 29.56%), and in C trials (8 trials, 767 patients) was 42.45% (35.67%-49.52%). In terms of subgroup differences, the difference in ORR was statistically significant between IO/C and IO trials (p= 0.0844) and between IO and chemotherapy trials (p< 0.0001) in the overall population. Similarly, we found a statistically significant difference in ORR between IO/C and IO (p= 0.0108) and between IO and chemotherapy trials (p< 0.0001) in the cisplatin-ineligible population. No statistically significant differences were observed between IO/C and C alone. Conclusions: First-line IO/C may achieve a better objective response compared to IO alone in patients diagnosed with locally advanced/metastatic UC. Although, there appears to be a trend of greater benefit with IO/C compared to C alone, the difference was not statistically significant. The results will be updated as soon data from new trials (CheckMate 901 and EV 302) becomes available which could offer new insights.

ORR
(95%CI)
IO/CIO aloneC alone
Overall population44.70%
[21.88%- 70.0%]
23.68%
[19.55%- 28.36%]
43.46%
[37.43%-49.68%]
Cisplatin ineligible population60.06%
[33.38%-81.86%]
26.15%
[23.01%; 29.56%]
42.45%
[35.67%-49.52%]

Disclaimer

This material on this page is ©2024 American Society of Clinical Oncology, all rights reserved. Licensing available upon request. For more information, please contact licensing@asco.org

Abstract Details

Meeting

2024 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session B: Urothelial Carcinoma

Track

Urothelial Carcinoma

Sub Track

Therapeutics

Citation

J Clin Oncol 42, 2024 (suppl 4; abstr 639)

DOI

10.1200/JCO.2024.42.4_suppl.639

Abstract #

639

Poster Bd #

J3

Abstract Disclosures