TY - JOUR
T1 - Bladder-sparing Therapy for Bacillus Calmette-Guérin–unresponsive Non–muscle-invasive Bladder Cancer
T2 - International Bladder Cancer Group Recommendations for Optimal Sequencing and Patient Selection
AU - Li, Roger
AU - Hensley, Patrick J.
AU - Gupta, Shilpa
AU - Al-Ahmadie, Hikmat
AU - Babjuk, Marko
AU - Black, Peter C.
AU - Brausi, Maurizio
AU - Bree, Kelly K.
AU - Fernández, Mario I.
AU - Guo, Charles C.
AU - Horowitz, Amir
AU - Lamm, Donald L.
AU - Lerner, Seth P.
AU - Lotan, Yair
AU - Mariappan, Paramananthan
AU - McConkey, David
AU - Mertens, Laura S.
AU - Mir, Carmen
AU - Ross, Jeffrey S.
AU - O'Donnell, Michael
AU - Palou, Joan
AU - Pohar, Kamal
AU - Steinberg, Gary
AU - Soloway, Mark
AU - Spiess, Philippe E.
AU - Svatek, Robert S.
AU - Tan, Wei Shen
AU - Taoka, Rikiya
AU - Buckley, Roger
AU - Kamat, Ashish M.
N1 - Publisher Copyright:
© 2024 European Association of Urology
PY - 2024/12
Y1 - 2024/12
N2 - Background and objective: There has been a recent surge in the development of agents for bacillus Calmette-Guérin–unresponsive (BCG-U) non–muscle-invasive bladder cancer (NMIBC). Critical assessment of these agents and practical recommendations for optimal selection of patients and therapies are urgently needed, especially in the absence of randomized trials on bladder-sparing treatment (BST) options. Methods: A global committee of bladder cancer experts was assembled to develop recommendations on BST for BCG-U NMIBC. Working groups reviewed the literature and developed draft recommendations, which were then voted on by International Bladder Cancer Group (IBCG) members using a modified Delphi process. During a live meeting in August 2023, voting results and supporting evidence were presented, and recommendations were refined on the basis of meeting discussions. Final recommendations achieved >75% agreement during the meeting, and some were further refined via web conferences and e-mail discussions. Key findings and limitations: There is currently no single optimal agent for patients with BCG-U disease who seek to avoid radical cystectomy (RC). BST selection should be personalized, taking into account individual patient characteristics and preferences, tumor attributes, and efficacy/toxicity data for the agents available. For patients with BCG-U carcinoma in situ (CIS), gemcitabine/docetaxel (GEM/DOCE), nadofaragene firadenovec (NFF), and nogapendekin alfa inbakicept-pmln (NAI) + BCG are recommended; because of its systemic toxicity, pembrolizumab should only be offered after other options are exhausted. For patients with BCG-U papillary-only tumors, GEM/DOCE, NFF, NAI + BCG, single-agent chemotherapy, hyperthermic mitomycin C, and pembrolizumab are recommended. Given the modest efficacy of available options, clinical trial participation is encouraged. For unapproved agents with reported data, IBCG recommendations await the final results of pivotal trials. Conclusions and clinical implications: The IBCG consensus recommendations provide practical guidance on BST for BCG-U NMIBC.
AB - Background and objective: There has been a recent surge in the development of agents for bacillus Calmette-Guérin–unresponsive (BCG-U) non–muscle-invasive bladder cancer (NMIBC). Critical assessment of these agents and practical recommendations for optimal selection of patients and therapies are urgently needed, especially in the absence of randomized trials on bladder-sparing treatment (BST) options. Methods: A global committee of bladder cancer experts was assembled to develop recommendations on BST for BCG-U NMIBC. Working groups reviewed the literature and developed draft recommendations, which were then voted on by International Bladder Cancer Group (IBCG) members using a modified Delphi process. During a live meeting in August 2023, voting results and supporting evidence were presented, and recommendations were refined on the basis of meeting discussions. Final recommendations achieved >75% agreement during the meeting, and some were further refined via web conferences and e-mail discussions. Key findings and limitations: There is currently no single optimal agent for patients with BCG-U disease who seek to avoid radical cystectomy (RC). BST selection should be personalized, taking into account individual patient characteristics and preferences, tumor attributes, and efficacy/toxicity data for the agents available. For patients with BCG-U carcinoma in situ (CIS), gemcitabine/docetaxel (GEM/DOCE), nadofaragene firadenovec (NFF), and nogapendekin alfa inbakicept-pmln (NAI) + BCG are recommended; because of its systemic toxicity, pembrolizumab should only be offered after other options are exhausted. For patients with BCG-U papillary-only tumors, GEM/DOCE, NFF, NAI + BCG, single-agent chemotherapy, hyperthermic mitomycin C, and pembrolizumab are recommended. Given the modest efficacy of available options, clinical trial participation is encouraged. For unapproved agents with reported data, IBCG recommendations await the final results of pivotal trials. Conclusions and clinical implications: The IBCG consensus recommendations provide practical guidance on BST for BCG-U NMIBC.
KW - Bacillus Calmette-Guérin–unresponsive non–muscle-invasive bladder cancer
KW - Bladder-sparing therapy
KW - Gemcitabine/docetaxel
KW - Gene-based therapy
KW - Immune checkpoint inhibitors
KW - Intravesical chemotherapy
KW - Nadofaragene firadenovec
KW - Nogapendekin alfa inbakicept-pmln
KW - Pembrolizumab
KW - Targeted treatments
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U2 - 10.1016/j.eururo.2024.08.001
DO - 10.1016/j.eururo.2024.08.001
M3 - Review article
C2 - 39183090
AN - SCOPUS:85202463250
SN - 0302-2838
VL - 86
SP - 516
EP - 527
JO - European Urology
JF - European Urology
IS - 6
ER -