Outcomes of additional BCG versus sequential gemcitabine + docetaxel in BCG-exposed high-risk non–muscle-invasive bladder cancer.

e16600 Background: For BCG-exposed high-risk (HR) non-muscle-invasive bladder cancer (NMIBC), current standard of care encompasses additional BCG treatment. However, data on therapies in this emerging disease space remain limited. Methods: A retrospective review was conducted on BCG-exposed HR NMIBC patients treated with additional BCG or sequential gemcitabine+docetaxel (GemDoce). BCG-exposed HR NMIBC was defined according to the 2022 IBCG statement. Clinicopathologic and oncologic outcomes, including high-grade (HG) recurrence-free survival (RFS) and progression-free survival (PFS), were captured. Kaplan-Meier (KM) analysis was used to estimate HG RFS and PFS with comparisons made using the log-rank test. Subgroup analysis was also performed on patients who declined or were unable to undergo radical cystectomy (RC). Results: 115 BCG-exposed patients with HR NMIBC were identified, of whom 48 (41.7%) received BCG, 51 received GemDoce (44.3%), and 16 (13.9%) did not receive further treatment. Overall, most patients were male (88.7%), with a median age of 75.9 years (IQR: 69.4-81.1), and median follow-up of 20.6 months (IQR: 11.3-35.7). Patients treated with sequential GemDoce received more BCG doses prior to BCG exposed HR NMIBC diagnosis (Table 1; p<0.001). On KM analysis, additional BCG and sequential GemDoce showed similar oncologic outcomes as measured by HG RFS (p=0.5). PFS was shown to be improved by either treatments over no treatment (p<0.001). These findings were mirrored in KM subgroup analysis after excluding patients who underwent RC at any point. Conclusions: We report that additional BCG and sequential GemDoce have similar efficacy in BCG-exposed HR NMIBC. Validation of these findings in a larger patient population may inform updated practice guidelines regarding BCG-exposed HR NMIBC. Baseline clinicopathologic variables of patients upon BCG exposed HR NMIBC diagnosis. All Patients Additional BCG Sequential GemDoce No treatment p Total patients, n 115 48 51 16 Age (years), median (IQR) 75.9 (69-.4-81.1) 76.6 (69.6-81.5) 75.3 (70.0-79.9) 76.1 (67.5-81.6) 0.8 Male, n (%) 102 (88.7) 44 (91.7) 45 (88.2) 13 (81.25) 0.5 Smoking exposure, n (%) 77 (67.0) 32 (66.7) 35 (68.6) 10 (62.5) 0.9 # of BCG doses previously received, median (IQR) 6 (6-12) 6 (6-6) 12 (6-15) 6 (6-9.25) <0.001 BCG exposed subpopulation, n (%) <0.001 BCG-resistant NMIBC 36 (31.3) 19 (39.6) 15 (29.4) 2 (12.5) Delayed relapse after inadequate BCG 45 (39.13) 25 (52.1) 12 (23.5) 8 (50.0) Delayed relapse after adequate BCG 34 (29.6) 4 (8.3) 24 (47.1) 6 (37.5) pT-Stage, n (%) 0.2 Ta 62 (53.9) 23 (47.9) 32 (62.8) 7 (43.75) T1 19 (16.5) 7 (14.6) 7 (13.7) 5 (31.25) Tis 34 (29.6) 18 (37.5) 12 (23.5) 4 (25.0) Concomitant CIS, n (%)

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Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.e16600
Primary Topic
Bladder and Urothelial Cancer Treatments
Type
article
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article

Outcomes of additional BCG versus sequential gemcitabine + docetaxel in BCG-exposed high-risk non–muscle-invasive bladder cancer.

Logan Zemp, Christian Harrs, Scott M. Gilbert, Wade J. Sexton et al.
Journal of Clinical Oncology
Bladder and Urothelial Cancer Treatments
article

Outcomes of additional BCG versus sequential gemcitabine + docetaxel in BCG-exposed high-risk non–muscle-invasive bladder cancer.

Logan Zemp, Christian Harrs, Scott M. Gilbert, Wade J. Sexton, Lexiaochuan Wen, Alice Yu, Philippe E. Spiess, Behzad Jazayeri, Roger Li, Joshua Linscott, Adnan Fazili, Michael Adam Poch, Christopher Guske, Hongzhi Xu
article en

Abstract

e16600 Background: For BCG-exposed high-risk (HR) non-muscle-invasive bladder cancer (NMIBC), current standard of care encompasses additional BCG treatment. However, data on therapies in this emerging disease space remain limited. Methods: A retrospective review was conducted on BCG-exposed HR NMIBC patients treated with additional BCG or sequential gemcitabine+docetaxel (GemDoce). BCG-exposed HR NMIBC was defined according to the 2022 IBCG statement. Clinicopathologic and oncologic outcomes, including high-grade (HG) recurrence-free survival (RFS) and progression-free survival (PFS), were captured. Kaplan-Meier (KM) analysis was used to estimate HG RFS and PFS with comparisons made using the log-rank test. Subgroup analysis was also performed on patients who declined or were unable to undergo radical cystectomy (RC). Results: 115 BCG-exposed patients with HR NMIBC were identified, of whom 48 (41.7%) received BCG, 51 received GemDoce (44.3%), and 16 (13.9%) did not receive further treatment. Overall, most patients were male (88.7%), with a median age of 75.9 years (IQR: 69.4-81.1), and median follow-up of 20.6 months (IQR: 11.3-35.7). Patients treated with sequential GemDoce received more BCG doses prior to BCG exposed HR NMIBC diagnosis (Table 1; p<0.001). On KM analysis, additional BCG and sequential GemDoce showed similar oncologic outcomes as measured by HG RFS (p=0.5). PFS was shown to be improved by either treatments over no treatment (p<0.001). These findings were mirrored in KM subgroup analysis after excluding patients who underwent RC at any point. Conclusions: We report that additional BCG and sequential GemDoce have similar efficacy in BCG-exposed HR NMIBC. Validation of these findings in a larger patient population may inform updated practice guidelines regarding BCG-exposed HR NMIBC. Baseline clinicopathologic variables of patients upon BCG exposed HR NMIBC diagnosis. All Patients Additional BCG Sequential GemDoce No treatment p Total patients, n 115 48 51 16 Age (years), median (IQR) 75.9 (69-.4-81.1) 76.6 (69.6-81.5) 75.3 (70.0-79.9) 76.1 (67.5-81.6) 0.8 Male, n (%) 102 (88.7) 44 (91.7) 45 (88.2) 13 (81.25) 0.5 Smoking exposure, n (%) 77 (67.0) 32 (66.7) 35 (68.6) 10 (62.5) 0.9 # of BCG doses previously received, median (IQR) 6 (6-12) 6 (6-6) 12 (6-15) 6 (6-9.25) <0.001 BCG exposed subpopulation, n (%) <0.001 BCG-resistant NMIBC 36 (31.3) 19 (39.6) 15 (29.4) 2 (12.5) Delayed relapse after inadequate BCG 45 (39.13) 25 (52.1) 12 (23.5) 8 (50.0) Delayed relapse after adequate BCG 34 (29.6) 4 (8.3) 24 (47.1) 6 (37.5) pT-Stage, n (%) 0.2 Ta 62 (53.9) 23 (47.9) 32 (62.8) 7 (43.75) T1 19 (16.5) 7 (14.6) 7 (13.7) 5 (31.25) Tis 34 (29.6) 18 (37.5) 12 (23.5) 4 (25.0) Concomitant CIS, n (%)

Journal of Clinical OncologyVol. 43(16_suppl)
University of South Florida (US), Moffitt Cancer Center (US)
Openalex Percentile: Top 79%
Bladder and Urothelial Cancer Treatments
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