Final Results from SAUL, a Single-arm International Study of Atezolizumab in Unselected
Patients with Pretreated Locally Advanced/Metastatic Urinary Tract Carcinoma
Sternberg, Cora N; Loriot, Yohann; Choy, Ernest; Castellano, Daniel; Lopez-Rios, Fernando; Banna, Giuseppe Luigi; Zengerling, Friedemann; De Giorgi, Ugo; Gedye, Craig; Masini, Cristina; Bamias, Aristotelis; Garcia Del Muro, Xavier; Duran, Ignacio; Powles, Thomas; Retz, Margitta; Gamulin, Marija; Geczi, Lajos [Géczi, Lajos (Onkológia), szerző] Országos Onkológiai Intézet; Huddart, Robert A; Calabrò, Fabio; Kandula, Geetha; Skamnioti, Pari; Merseburger, Axel S
We assessed the safety of atezolizumab in unselected patients (including understudied
populations typically excluded from clinical trials) with pretreated urinary tract
carcinoma (UTC). The prespecified final analysis updates previously reported safety
and efficacy data.The single-arm prospective SAUL study (NCT02928406) enrolled 1004
patients with locally advanced/metastatic urothelial/non-urothelial UTC that had progressed
during/after one to three prior treatment lines for advanced UTC (or <12 mo after
[neo]adjuvant therapy). Broad eligibility criteria allowed enrollment of patients
with complex comorbidities approximating the real-world setting. Patients received
atezolizumab 1200 mg every 3 wk until disease progression or unacceptable toxicity.
The primary endpoint was safety. Secondary endpoints included duration of response
and overall survival (OS).The treated cohort included 10% of patients with poor performance
status, 5% with creatinine clearance <30 ml/min, and 4% with autoimmune disease. At
median follow-up of 55 mo, median atezolizumab duration was 2.8 mo (range 0-62); 68
patients (7%) continued atezolizumab for >4 yr. Treatment-related grade ≥3 adverse
events occurred in 16% of patients (death in 1%); 8% discontinued atezolizumab for
adverse events. Median OS was 8.6 mo (95% confidence interval 7.8-9.7) and 136 patients
(14%) had OS longer than 4 yr. Limitations include the small sample size for some
subgroups of special interest.Long-term safety and efficacy data continue to show
a benefit of atezolizumab in unselected patients with UTC. Remarkably, 14% of patients
lived for >4 yr after starting atezolizumab. These results can inform multidisciplinary
team discussions and treatment decision-making for patients with UTC with complex
comorbidities.The SAUL study looked at how well tolerated a drug called atezolizumab
was in patients with urinary tract cancer who had already received up to three previous
treatments for their cancer, including people who are usually not included in clinical
trials because of other medical conditions. The length of survival after starting
treatment was also assessed. Overall, the results show that atezolizumab was well
tolerated. People for whom other therapies had failed lived for about 8.6 months on
average after starting treatment, and 14% of the patients were still alive after 4
years.