Clinical outcomes of chemotherapy with or without intravesical BCG in NMIBC patients: A Bayesian network meta-analysis.

e16599 Background: Non-muscle-invasive bladder cancer (NMIBC) is a recurrent urinary bladder malignancy traditionally treated with intravesical Bacillus Calmette–Guérin (BCG). Newer chemotherapeutics combined with BCG may enhance efficacy and safety, though clinical outcomes remain less-explored. We evaluated BCG monotherapy versus combination therapies through systematic review and network meta-analysis. Methods: A systematic literature search of 4 databases identified primary studies on chemotherapeutics with or without BCG in NMIBC. A Bayesian network meta-analysis was performed in R with pooled risk ratios (RR) with 95% credible intervals (CrI) using random or common effects models based on the Deviance Information Criterion (DIC), with quantification of surface under the cumulative ranking (SUCRA). Results: Our analysis included 19 studies (7,514 patients). For Complete Response (CR), Radiofrequency-Induced Thermo-chemotherapeutic Effect Mitomycin C (RITE-MMC) ranked highest (SUCRA: 91.22) but was less effective than BCG (RR: 0.52, CrI: 0.20–1.30). Chemohyperthermia (CHT), Sequential MMC+BCG and hyperthermic intravesical chemotherapy (HIVEC) showed comparable efficacy to BCG (RRs: 1.04, 1.05). HIVEC (RR: 0.11, CrI: 0.00–0.66, SUCRA: 87) and titanium glycerosolvate aquacomplex (TGA) (RR: 0.11, CrI: 0.00–0.76, SUCRA: 86.26) demonstrated superior efficacy in Progressive Disease (PD). For Recurrence Rate (RR), Neoadjuvant electromotive MMC (EMDA)+BCG ranked highest (SUCRA: 83.51, RR: 0.22, CrI: 0.02–2.19), followed by Sequential MMC+BCG (SUCRA: 65.82). Sequential MMC+BCG (SUCRA: 100, RR: 0.48, CrI: 0.35–0.67) significantly outperformed BCG (SUCRA: 62.77) in prolonging Recurrence-Free Survival (RFS). Conclusions: Our findings demonstrated Sequential MMC+BCG shows promise for improving recurrence-free survival and recurrence rates. HIVEC and intravesical gemcitabine demonstrated superior safety with fewer adverse events, offering valuable insights to optimize NMIBC treatment strategies. Outcome/Intervention (RR, CrI, SUCRA value) Neoadjuvant EMDA+BCG RITE Sequential MMC+BCG HIVEC BEXIDEM IV-Thiotepa BCG (SUCRA) Intravesical gemcitabine PD - - 0.51,0.30-0.85,55.65 0.11,0.00-0.66,87 - 1.03,0.62-1.72,17.22 17.95 0.49,0.13-1.53,53.64 RR 0.22,0.02-2.19,83.51 0.56,0.07-4.62,61.61 0.52,0.12-2.33,65.82 0.49,0.05-4.94,64.49 2.84,0.33-24.59,16.44 0.67,0.08-5.43,56.27 40.52 0.64,0.14-2.95,58.28 RFS - - 0.48,0.35-0.67,100 1.18,0.94-1.53,19.67 - - 62.77 NA Total Adverse Events - - 0.68,0.06-7.97,50.51 0.42,0.06-2.43,66.58 - 0.81,0.07-9.78,45.37 35.44 0.16,0.01-2.17,84.35 Hematuria 0.48,0.06-2.38,63.59 1.01,0.60-1.69,32.56 - 0.28,0.01-2.34,75.27 - 0.31,0.04-1.31,78.03 34.18 0.42,0.01-5.11,62.65 Dysuria - 0.85,0.14-4.93,39.37 - - 0.29,0.04-1.81,76.61 0.43,0.05-3.21,63.15 28.5 -

Authors

Institutions

Publication Details

Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.e16599
Primary Topic
Bladder and Urothelial Cancer Treatments
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Clinical outcomes of chemotherapy with or without intravesical BCG in NMIBC patients: A Bayesian network meta-analysis.

Hurriyah Ramzan, Danisha Kumar, Uazman Alam, Victor Ghosh et al.
Journal of Clinical Oncology
Bladder and Urothelial Cancer Treatments
article

Clinical outcomes of chemotherapy with or without intravesical BCG in NMIBC patients: A Bayesian network meta-analysis.

Hurriyah Ramzan, Danisha Kumar, Uazman Alam, Victor Ghosh, Mohamed Mansour, Waseem Nabi, Fatima Sajjad, Madona Pakkam, Rameez Qasim, Md. Rafiqul Islam, Nouman Aziz, Arwa M Ibrahim, Shree Rath, Muzamil Khan
article en

Abstract

e16599 Background: Non-muscle-invasive bladder cancer (NMIBC) is a recurrent urinary bladder malignancy traditionally treated with intravesical Bacillus Calmette–Guérin (BCG). Newer chemotherapeutics combined with BCG may enhance efficacy and safety, though clinical outcomes remain less-explored. We evaluated BCG monotherapy versus combination therapies through systematic review and network meta-analysis. Methods: A systematic literature search of 4 databases identified primary studies on chemotherapeutics with or without BCG in NMIBC. A Bayesian network meta-analysis was performed in R with pooled risk ratios (RR) with 95% credible intervals (CrI) using random or common effects models based on the Deviance Information Criterion (DIC), with quantification of surface under the cumulative ranking (SUCRA). Results: Our analysis included 19 studies (7,514 patients). For Complete Response (CR), Radiofrequency-Induced Thermo-chemotherapeutic Effect Mitomycin C (RITE-MMC) ranked highest (SUCRA: 91.22) but was less effective than BCG (RR: 0.52, CrI: 0.20–1.30). Chemohyperthermia (CHT), Sequential MMC+BCG and hyperthermic intravesical chemotherapy (HIVEC) showed comparable efficacy to BCG (RRs: 1.04, 1.05). HIVEC (RR: 0.11, CrI: 0.00–0.66, SUCRA: 87) and titanium glycerosolvate aquacomplex (TGA) (RR: 0.11, CrI: 0.00–0.76, SUCRA: 86.26) demonstrated superior efficacy in Progressive Disease (PD). For Recurrence Rate (RR), Neoadjuvant electromotive MMC (EMDA)+BCG ranked highest (SUCRA: 83.51, RR: 0.22, CrI: 0.02–2.19), followed by Sequential MMC+BCG (SUCRA: 65.82). Sequential MMC+BCG (SUCRA: 100, RR: 0.48, CrI: 0.35–0.67) significantly outperformed BCG (SUCRA: 62.77) in prolonging Recurrence-Free Survival (RFS). Conclusions: Our findings demonstrated Sequential MMC+BCG shows promise for improving recurrence-free survival and recurrence rates. HIVEC and intravesical gemcitabine demonstrated superior safety with fewer adverse events, offering valuable insights to optimize NMIBC treatment strategies. Outcome/Intervention (RR, CrI, SUCRA value) Neoadjuvant EMDA+BCG RITE Sequential MMC+BCG HIVEC BEXIDEM IV-Thiotepa BCG (SUCRA) Intravesical gemcitabine PD - - 0.51,0.30-0.85,55.65 0.11,0.00-0.66,87 - 1.03,0.62-1.72,17.22 17.95 0.49,0.13-1.53,53.64 RR 0.22,0.02-2.19,83.51 0.56,0.07-4.62,61.61 0.52,0.12-2.33,65.82 0.49,0.05-4.94,64.49 2.84,0.33-24.59,16.44 0.67,0.08-5.43,56.27 40.52 0.64,0.14-2.95,58.28 RFS - - 0.48,0.35-0.67,100 1.18,0.94-1.53,19.67 - - 62.77 NA Total Adverse Events - - 0.68,0.06-7.97,50.51 0.42,0.06-2.43,66.58 - 0.81,0.07-9.78,45.37 35.44 0.16,0.01-2.17,84.35 Hematuria 0.48,0.06-2.38,63.59 1.01,0.60-1.69,32.56 - 0.28,0.01-2.34,75.27 - 0.31,0.04-1.31,78.03 34.18 0.42,0.01-5.11,62.65 Dysuria - 0.85,0.14-4.93,39.37 - - 0.29,0.04-1.81,76.61 0.43,0.05-3.21,63.15 28.5 -

Journal of Clinical OncologyVol. 43(16_suppl)
Andhra University (IN), Khyber Medical College (PK), Zagazig University (EG), George Washington University (US), Allama Iqbal Medical College (PK), Wyckoff Heights Medical Center (US), University of Sharjah (AE), Dow University of Health Sciences (PK), All India Institute of Medical Sciences Bhubaneswar (IN), Shaheed Suhrawardy Medical College (BD)
Openalex Percentile: Top 79%
Bladder and Urothelial Cancer Treatments
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.