Abstract 2012P
Background
Urothelial cancer (UC), especially with bone metastases, poses significant clinical challenges. Despite its occurrence in 25% to 47% of cases, with 5% to 15% experiencing exclusive bone metastasis, it remains underrecognized and challenging to treat. Despite the approval of multiple immune checkpoint inhibitors (ICIs), the survival benefit with ICIs in those with bone metastasis remains unclear. None of the randomized studies specifically investigated the outcomes and efficacy of bone metastases in subgroup analyses. We aim to assess the role and efficacy of ICIs in UC patients with bone metastases using the National Cancer Database (NCDB).
Methods
Using NCDB, we included de-novo metastatic UC cases (2017-2021). We subcategorized patients into bone-only metastases (BoM), bone (B) + brain metastases (mets), B + visceral mets (liver/lung), and B + lymph nodes. Demographics included primary site, first-line treatment (chemo/immunotherapy), age, race, gender, and survival status. OS was analyzed via Kaplan-Meier curves, Log-rank tests, and Cox proportional hazards model.
Results
3971 eligible UC cases were included. Primary sites were kidney/renal pelvis (82.4%), bladder (12.4%), and ureter (2.6%). BoM occurred in 27%, B + brain in 11%, B + visceral in 51%, and B+ lymph nodes in 11%. 48.1% received first-line chemo, 51.9% first-line ICIs. Most were aged 40-64 (40%), white (84.8%), and male (70%). Patients with B + brain mets had the worst outcomes (HR 1.58, p<0.001), followed by B + visceral mets (HR 1.48, p<0.001), and B + lymph node mets (HR 1.25, p=0.007) compared to BoM. In multivariate analysis, patients receiving first-line chemotherapy had worse outcomes than first-line immunotherapy (HR 1.24, p<0.001) in all cohorts. However, when specifically analyzing the treatment difference among BoM patients, no survival disparity was observed between chemo and ICIs (p=0.32).
Conclusions
Interestingly, our analysis revealed that upper tract UC displays a significantly heightened propensity for bone metastases compared to lower tract UC. Moreover, patients with de-novo metastatic UC with bone met who underwent first line chemo experienced poor outcomes relative to those treated with first-line ICIs.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
2007P - Similar genetic profile in early and late-stage urothelial tract cancer suggests that early genomic testing bears the potential of timely personalized treatment in clinical trials
Presenter: Dag Rune Stormoen
Session: Poster session 13
2008P - Assessing response durability and survival after second-line pembrolizumab in advanced urothelial carcinoma: A multicenter validation of a risk model
Presenter: Samer Salah
Session: Poster session 13
2010P - Trifunctional anti-EpCAM/CD3 bsAb catumaxomab intravesically for high and intermediate risk non muscle invasive bladder cancer (HMR-NMIBC): Interim analysis of a phase I study
Presenter: Aleksander Antoniewicz
Session: Poster session 13
2011P - Neoadjuvant immunotherapy-driven bladder preservation for muscle-invasive bladder cancer: A multicenter, propensity score-matched cohort study
Presenter: Jiao Hu
Session: Poster session 13
2013P - First preliminary results of artificial intelligence generated treatment recommendations for urothelial cancer based on multidisciplinary cancer conferences from the KITTU project
Presenter: Gregor Duwe
Session: Poster session 13
2014P - Overall survival (OS) results in phase II trial of cabozantinib (CABO) plus durvalumab (DURVA) in patients with urothelial carcinoma (UC) or non-UC variant histologies (VH) after platinum chemotherapy (ARCADIA)
Presenter: Patrizia Giannatempo
Session: Poster session 13
2015P - Serum nectin-4: Prognostic and predictive value in bladder cancer?
Presenter: Kerstin Junker
Session: Poster session 13
2016P - Evaluation of event-free survival (EFS) as a surrogate endpoint for overall survival (OS) in muscle-invasive bladder cancer (MIBC) following neoadjuvant (NAD) therapy
Presenter: Cora Sternberg
Session: Poster session 13
2017P - Intrinsic molecular difference between bladder and upper tract urothelial carcinomas and its impacts in treatment response
Presenter: Jiwon Kim
Session: Poster session 13