Bladder-sparing Therapy for Bacillus Calmette-Guérin-unresponsive Non-muscle-invasive Bladder Cancer: International Bladder Cancer Group Recommendations for Optimal Sequencing and Patient Selection

被引:0
作者
Li, Roger [1 ]
Hensley, Patrick J. [2 ]
Gupta, Shilpa [3 ]
Al-Ahmadie, Hikmat [4 ]
Babjuk, Marko [5 ]
Black, Peter C. [6 ]
Brausi, Maurizio [7 ]
Bree, Kelly K. [8 ]
Fernandez, Mario I. [9 ]
Guo, Charles C. [10 ]
Horowitz, Amir [11 ,12 ,13 ]
Lamm, Donald L. [14 ]
Lerner, Seth P. [15 ]
Lotan, Yair [16 ]
Mariappan, Paramananthan [17 ]
Mcconkey, David [18 ]
Mertens, Laura S. [19 ]
Mir, Carmen [20 ]
Ross, Jeffrey S. [21 ,22 ]
O'Donnell, Michael
Palou, Joan
Pohar, Kamal [23 ]
Steinberg, Gary [24 ]
Soloway, Mark [25 ]
Spiess, Philippe E. [26 ]
Svatek, Robert S. [27 ]
Tan, Wei Shen [8 ]
Taoka, Rikiya [28 ]
Buckley, Roger [29 ]
Kamat, Ashish M. [8 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Genitourinary Oncol, Tampa, FL USA
[2] Univ Kentucky, Coll Med, Dept Urol, Lexington, KY USA
[3] Cleveland Clin, Taussig Canc Inst, Cleveland, OH USA
[4] Mem Sloan Kettering Canc Ctr, Dept Pathol & Lab Med, New York, NY USA
[5] Charles Univ Prague, Univ Hosp Motol, Fac Med 2, Dept Urol, Prague, Czech Republic
[6] Univ British Columbia, Dept Urol Sci, Vancouver, BC, Canada
[7] Hesperia Hosp, Dept Urol, Modena, Italy
[8] Univ Texas MD Anderson Canc Ctr, Dept Urol, 1515 Holcombe Blvd, Houston, TX 77030 USA
[9] Clin Alemana Univ Desarrollo, Dept Urol, Santiago, Chile
[10] Univ Texas MD Anderson Canc Ctr, Dept Anat Pathol, Houston, TX USA
[11] Icahn Sch Med Mt Sinai, Lipschultz Precis Immunol Inst, Dept Immunol & Immunotherapy, New York, NY USA
[12] Icahn Sch Med Mt Sinai, Lipschultz Precis Immunol Inst, Dept Oncol Sci, New York, NY USA
[13] Tisch Canc Inst, Icahn Sch Med Mt Sinai, New York, NY USA
[14] Univ Arizona, BCG Oncol PC, Coll Med, Phoenix, AZ USA
[15] Baylor Coll Med, Dan L Duncan Canc Ctr, Scott Dept Urol, Houston, TX USA
[16] UT Southwestern Med Ctr, Dept Urol, Dallas, TX USA
[17] Univ Edinburgh, Western Gen Hosp, Dept Urol, Edinburgh Bladder Canc Surg, Edinburgh, Scotland
[18] Johns Hopkins Greenberg Bladder Canc Inst, Baltimore, MD USA
[19] Antoni van Leeuwenhoek Hosp, Netherlands Canc Inst, Amsterdam, Netherlands
[20] Hosp Univ La Ribera, Dept Radiol, Valencia, Spain
[21] Upstate Med Univ, Syracuse, NY USA
[22] Fdn Med, Boston, MA USA
[23] Ohio State Univ, Dept Urol, Columbus, OH USA
[24] Rush Univ, Med Ctr, Dept Urol, Chicago, IL USA
[25] Mem Hosp, Hollywood, FL USA
[26] Univ S Florida, Moffitt Canc Ctr, Morsani Coll Med, Tampa, FL 33620 USA
[27] Univ Texas Hlth San Antonio, Dept Urol, San Antonio, TX USA
[28] Kagawa Univ, Fac Med, Kagawa, Japan
[29] North York Gen Hosp, Toronto, ON, Canada
关键词
bladder cancer; Bladder-sparing therapy; Intravesical chemotherapy; Immune checkpoint inhibitors; Gene-based therapy; Targeted treatments; Gemcitabine/docetaxel; Bacillus Calmette-Gu & eacute; rin-unre; Pembrolizumab; sponsive non-muscle-invasive; Nadofaragene firadenovec; Nogapendekin alfa inbakicept-pmln; CALMETTE-GUERIN THERAPY; CARCINOMA IN-SITU; PHASE-II; MITOMYCIN-C; SINGLE-ARM; UROTHELIAL CARCINOMA; OPEN-LABEL; EFFICACY; GEMCITABINE; SURVIVAL;
D O I
暂无
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background and objective: There has been a recent surge in the development of agents for bacillus Calmette-Gu & eacute;rin-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. (c) 2024 European Association of Urology. Published by Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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页码:516 / 527
页数:12
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