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Clinical Trial
. 2025 Jan 2;392(1):45-55.
doi: 10.1056/NEJMoa2401726. Epub 2024 Sep 15.

Adjuvant Pembrolizumab versus Observation in Muscle-Invasive Urothelial Carcinoma

Affiliations
Clinical Trial

Adjuvant Pembrolizumab versus Observation in Muscle-Invasive Urothelial Carcinoma

Andrea B Apolo et al. N Engl J Med. .

Abstract

Background: Muscle-invasive urothelial carcinoma is an aggressive disease with high rates of relapse. Whether pembrolizumab as adjuvant therapy would be effective in patients with high-risk muscle-invasive urothelial carcinoma after radical surgery is unknown.

Methods: In this phase 3 trial, we randomly assigned patients, in a 1:1 ratio, to receive pembrolizumab at a dose of 200 mg every 3 weeks for 1 year or to undergo observation. Randomization was stratified according to pathological stage, centrally tested programmed death ligand 1 (PD-L1) status, and previous neoadjuvant chemotherapy. The coprimary end points were disease-free survival and overall survival in the intention-to-treat population. We considered the trial to be successful if either disease-free survival or overall survival was significantly longer with pembrolizumab than with observation.

Results: A total of 702 patients underwent randomization; 354 were assigned to receive pembrolizumab, and 348 were assigned to observation. As of July 5, 2024, the median duration of follow-up for disease-free survival was 44.8 months. The median disease-free survival was 29.6 months (95% confidence interval [CI], 20.0 to 40.7) with pembrolizumab and 14.2 months (95% CI, 11.0 to 20.2) with observation (hazard ratio for disease progression or death, 0.73; 95% CI, 0.59 to 0.90; two-sided P = 0.003). Grade 3 or higher adverse events (regardless of attribution) occurred in 50.6% of the patients in the pembrolizumab group and in 31.6% of the patients in the observation group.

Conclusions: Among patients with high-risk muscle-invasive urothelial carcinoma after radical surgery, disease-free survival was significantly longer with adjuvant pembrolizumab than with observation. (Funded by the National Cancer Institute of the National Institutes of Health and others; Alliance A031501 AMBASSADOR ClinicalTrials.gov number, NCT03244384.).

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Figures

Figure 1:
Figure 1:. Disease-Free Survival
Kaplan-Meier plots for disease-free survival in the intention-to-treat population. HR=hazard ratio. Tick marks indicate patient censored at the last disease evaluation prior to analysis or treatment with alternative therapy prior to a disease-free survival event.
Figure 2:
Figure 2:. Disease-Free Survival by PD-L1 Status
Kaplan-Meier plots for disease-free survival based on A] PD-L1 negative tumors and B] PD-L1 positive tumors HR=hazard ratio. Tick marks indicate patient censored at the last disease evaluation prior to analysis or treatment with alternative therapy prior to a disease-free survival event.
Figure 3:
Figure 3:. Disease-Free Survival Subgroup Analysis in the Intention-to-Treat Population
Hazard ratios and two-sided 95% confidence intervals were estimated with the use of a stratified Cox regression model for disease-free survival. Confidence intervals are not adjusted for multiplicity.
Figure 4:
Figure 4:. Overall Survival
Kaplan-Meier plots for preliminary overall survival in the intention-to-treat population. HR=hazard ratio. Tick marks indicate data censored at the follow-up.

References

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