Adjuvant Immune Checkpoint Inhibitors for Muscle-Invasive Urothelial Carcinoma: An Updated Systematic Review, Meta-analysis, and Network Meta-analysis

被引:0
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作者
Yanagisawa, Takafumi [1 ,2 ]
Mori, Keiichiro [1 ,2 ]
Matsukawa, Akihiro [1 ,2 ]
Kawada, Tatsushi [1 ,3 ]
Katayama, Satoshi [1 ,3 ]
Laukhtina, Ekaterina [1 ,4 ]
Rajwa, Pawel [1 ,5 ]
Quhal, Fahad [1 ,6 ]
Pradere, Benjamin [1 ,7 ]
Fukuokaya, Wataru [2 ]
Iwatani, Kosuke [2 ]
Afferi, Luca [8 ]
Marcq, Gautier [9 ]
Mertens, Laura S. [10 ]
Gallioli, Andrea [11 ]
Tully, Karl H. [12 ]
Cano-Velasco, Jorge [13 ]
Subiela, Jose Daniel [14 ]
Abu-Ghanem, Yasmin [15 ]
Grobet-Jeandin, Elisabeth [16 ]
Del Giudice, Francesco [17 ]
Pichler, Renate [18 ]
Teoh, Jeremy Yuen-Chun [19 ]
Moschini, Marco [20 ]
Krajewski, Wojciech [21 ]
Miki, Jun [2 ]
Shariat, Shahrokh F. [1 ,22 ,23 ,24 ,25 ,26 ]
Kimura, Takahiro [2 ]
机构
[1] Med Univ Vienna, Comprehens Canc Ctr, Dept Urol, Vienna, Austria
[2] Jikei Univ Sch Med, Dept Urol, Dept Psychiat, 3-19-18 Nishi Shimbashi,Minato Ku, Tokyo 1058471, Japan
[3] Okayama Univ Grad Sch Med, Grad Sch Med Dent & Pharmaceut Sci, Dent & Pharmaceut Sci, Okayama, Japan
[4] Sechenov Univ, Inst Urol & Reprod Hlth, Moscow, Russia
[5] Ctr Postgrad Med Educ, Dept Urol 2, Warsaw, Poland
[6] King Fahad Specialist Hosp, Dept Urol, Dammam, Saudi Arabia
[7] La Croix Du Sud Hosp, Dept Urol, Quint Fonsegrives, France
[8] Luzerner Kantonsspital, Dept Urol, Luzern, Switzerland
[9] CHU Lille, Claude Huriez Hosp, Dept Urol, F-59000 Lille, France
[10] Antoni van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Urol, NL-1066 CX Amsterdam, Netherlands
[11] Autonomous Univ Barcelona, Dept Urol, Fdn Puigvert, Barcelona, Spain
[12] Ruhr Univ Bochum, Marien Hosp Herne, Dept Urol & Neurourol, Herne, Germany
[13] Gregorio Maranon Univ Hosp, Dept Urol, Madrid 28007, Spain
[14] Univ Alcala, Hosp Univ Ramon & Cajal, Dept Urol, IRYCIS, Madrid, Spain
[15] Royal Free Hosp, Specialist Ctr Kidney Canc, London, England
[16] Geneva Univ Hosp, Div Urol, Geneva, Switzerland
[17] Sapienza Univ Rome, Policlin Umberto Hosp 1, Dept Maternal Infant & Urol Sci, I-00161 Rome, Italy
[18] Med Univ Innsbruck, Comprehens Canc Ctr Innsbruck CCCI, Dept Urol, Innsbruck, Austria
[19] Chinese Univ Hong Kong, SH Ho Urol Ctr, Dept Surg, Hong Kong, Peoples R China
[20] San Raffaele Hosp & Sci Inst, Dept Urol, Milan, Italy
[21] Wroclaw Med Univ, Dept Minimally Invas & Robot Urol, Wroclaw, Poland
[22] Univ Jordan, Dept Special Surg, Div Urol, Amman, Jordan
[23] Univ Texas Southwestern Med Ctr, Dept Urol, Dallas, TX USA
[24] Charles Univ Prague, Fac Med 2, Dept Urol, Prague, Czech Republic
[25] Weill Cornell Med Coll, Dept Urol, New York, NY USA
[26] Karl Landsteiner Inst Urol & Androl, Vienna, Austria
关键词
RADICAL CYSTECTOMY; BLADDER-CANCER; NEOADJUVANT CHEMOTHERAPY; OPEN-LABEL; SURVIVAL; THERAPY;
D O I
10.1007/s11523-024-01114-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ContextAdjuvant immune checkpoint inhibitors (ICIs) have recently emerged as guideline-recommended treatments of high-risk muscle-invasive urothelial carcinoma (MIUC). However, there is limited evidence regarding the optimal candidates and the differential efficacy of adjuvant ICI regimens.ObjectiveTo synthesize and compare the efficacy and safety of adjuvant ICIs for high-risk MIUC using updated data from phase III randomized controlled trials.Evidence AcquisitionIn April 2024, three databases were searched for eligible randomized controlled trials that evaluated oncologic outcomes in patients with MIUC treated with adjuvant ICIs. Pairwise meta-analysis (MA) and network meta-analyses were performed to compare the hazard ratios of oncological outcomes, including disease-free survival (DFS), overall survival (OS), and adverse events. Subgroup analyses were conducted on the basis of predefined clinicopathological features.Evidence SynthesisThree randomized controlled trials that assessed the efficacy of adjuvant nivolumab, pembrolizumab, and atezolizumab were included in the MAs and network meta-analyses groups. Pairwise MAs showed that treatment with adjuvant ICIs significantly improved DFS [hazards ratio: 0.77, 95% confidence interval (CI): 0.66-0.90] as well as OS (hazards ratio: 0.87, 95% CI 0.76-1.00) in patients with MIUC compared with in the placebo/observation group. The DFS benefit was prominent in patients who underwent neoadjuvant chemotherapy (P = 0.041) and in those with bladder cancer (P = 0.013) but did not differ across programmed death-ligand 1 and lymph node status. Adjuvant ICI therapy was associated with increased risk of any (OR: 2.98, 95% CI 2.06-4.33) and severe adverse events (OR: 1.78, 95% CI 1.49-2.13). The treatment rankings revealed that pembrolizumab for DFS (84%) and nivolumab for OS (93%) had the highest likelihood of improving survival.ConclusionsOur analyses demonstrated the DFS and OS benefits of adjuvant ICIs for high-risk MIUC. Furthermore, patients with bladder cancer who underwent neoadjuvant chemotherapy appeared to be the optimal candidates for adjuvant ICIs regarding prolonged DFS. Adjuvant ICIs are the standard of care for high-risk MIUC, and differential clinical behaviors and efficacy will enrich clinical decision-making.
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页码:57 / 69
页数:13
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