-
Je něco špatně v tomto záznamu ?
Novel combination therapy for platinum-eligible patients with locally advanced or metastatic urothelial carcinoma: a systematic review and network meta-analysis
T. Yanagisawa, K. Mori, A. Matsukawa, T. Kawada, S. Katayama, E. Laukhtina, P. Rajwa, F. Quhal, B. Pradere, W. Fukuokaya, K. Iwatani, R. Pichler, JY. Teoh, M. Moschini, W. Krajewski, J. Miki, SF. Shariat, T. Kimura, European Association of...
Jazyk angličtina Země Německo
Typ dokumentu časopisecké články, systematický přehled, metaanalýza, přehledy
NLK
Directory of Open Access Journals
od 2024
PubMed Central
od 1982
Springer Journals Complete - Open Access
od 2024-01-01
Springer Nature OA/Free Journals
od 2024-01-01
- MeSH
- humanizované monoklonální protilátky terapeutické užití aplikace a dávkování škodlivé účinky MeSH
- inhibitory kontrolních bodů * terapeutické užití MeSH
- karcinom z přechodných buněk farmakoterapie mortalita patologie MeSH
- lidé MeSH
- metastázy nádorů MeSH
- monoklonální protilátky MeSH
- nádory močového měchýře farmakoterapie patologie mortalita MeSH
- protokoly protinádorové kombinované chemoterapie * terapeutické užití škodlivé účinky MeSH
- randomizované kontrolované studie jako téma MeSH
- síťová metaanalýza * MeSH
- urologické nádory farmakoterapie mortalita patologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- metaanalýza MeSH
- přehledy MeSH
- systematický přehled MeSH
Recent phase 3 randomized controlled trials (RCTs) demonstrate the promising impact of immune checkpoint inhibitor (ICI)-based combination therapies on locally advanced or metastatic urothelial carcinoma (UC). However, comparative data on the efficacy and toxicity of different ICI-based combinations are lacking. This study aims to compare the efficacy of first-line ICI-based combination therapies for locally advanced or metastatic UC using phase 3 RCT data. In November 2023, three databases were searched for RCTs evaluating oncological outcomes in patients with locally advanced or metastatic UC who were treated with first-line ICI-based combination therapies. Network meta-analysis (NMA) was conducted to compare outcomes, including overall survival (OS), progression-free survival (PFS), objective response rates (ORRs), complete response rates (CRRs), and treatment-related adverse events (TRAEs). Subgroup analyses were based on PD-L1 status and cisplatin eligibility. The NMA included five RCTs. Enfortumab vedotin (EV) + pembrolizumab ranked the highest for improving OS (100%), PFS (100%), ORR (96%), and CRR (96%), followed by nivolumab + chemotherapy. EV + pembrolizumab combination superiority held across PD-L1 status and cisplatin eligibility. In patients who are cisplatin-eligible, EV + pembrolizumab significantly improved OS (HR: 0.68, 95%CI 0.47-0.99) and PFS (HR: 0.67, 95%CI 0.49-0.92) compared to nivolumab + chemotherapy. Durvalumab + tremelimumab was the safest combination for severe TRAEs, and EV + pembrolizumab ranked second. Our analyses support EV + pembrolizumab combination as a first-line treatment for locally advanced or metastatic UC. Thus, EV + pembrolizumab may become a guideline-changing standard treatment.
Department of Minimally Invasive and Robotic Urology Wrocław Medical University Wrocław Poland
Department of Urology 2nd Faculty of Medicine Charles University Prague Czech Republic
Department of Urology King Fahad Specialist Hospital Dammam Saudi Arabia
Department of Urology La Croix Du Sud Hospital Quint Fonsegrives France
Department of Urology Medical University of Silesia Zabrze Poland
Department of Urology San Raffaele Hospital and Scientific Institute Milan Italy
Department of Urology The Jikei University School of Medicine Tokyo Japan
Department of Urology University of Texas Southwestern Medical Center Dallas TX USA
Department of Urology Weill Cornell Medical College New York NY USA
Division of Urology Department of Special Surgery The University of Jordan Amman Jordan
Institute for Urology and Reproductive Health Sechenov University Moscow Russia
Karl Landsteiner Institute of Urology and Andrology Vienna Austria
S H Ho Urology Centre Department of Surgery The Chinese University of Hong Kong Hong Kong China
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25010008
- 003
- CZ-PrNML
- 005
- 20250429134529.0
- 007
- ta
- 008
- 250415s2025 gw f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s00262-024-03910-3 $2 doi
- 035 __
- $a (PubMed)39891702
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a gw
- 100 1_
- $a Yanagisawa, Takafumi $u Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Wahringer Gurtel 18-20, 1090, Vienna, Austria $u Department of Urology, The Jikei University School of Medicine, Tokyo, Japan
- 245 10
- $a Novel combination therapy for platinum-eligible patients with locally advanced or metastatic urothelial carcinoma: a systematic review and network meta-analysis / $c T. Yanagisawa, K. Mori, A. Matsukawa, T. Kawada, S. Katayama, E. Laukhtina, P. Rajwa, F. Quhal, B. Pradere, W. Fukuokaya, K. Iwatani, R. Pichler, JY. Teoh, M. Moschini, W. Krajewski, J. Miki, SF. Shariat, T. Kimura, European Association of Urology–Young Academic Urologists Urothelial Carcinoma Working Group (EAU-YAU)
- 520 9_
- $a Recent phase 3 randomized controlled trials (RCTs) demonstrate the promising impact of immune checkpoint inhibitor (ICI)-based combination therapies on locally advanced or metastatic urothelial carcinoma (UC). However, comparative data on the efficacy and toxicity of different ICI-based combinations are lacking. This study aims to compare the efficacy of first-line ICI-based combination therapies for locally advanced or metastatic UC using phase 3 RCT data. In November 2023, three databases were searched for RCTs evaluating oncological outcomes in patients with locally advanced or metastatic UC who were treated with first-line ICI-based combination therapies. Network meta-analysis (NMA) was conducted to compare outcomes, including overall survival (OS), progression-free survival (PFS), objective response rates (ORRs), complete response rates (CRRs), and treatment-related adverse events (TRAEs). Subgroup analyses were based on PD-L1 status and cisplatin eligibility. The NMA included five RCTs. Enfortumab vedotin (EV) + pembrolizumab ranked the highest for improving OS (100%), PFS (100%), ORR (96%), and CRR (96%), followed by nivolumab + chemotherapy. EV + pembrolizumab combination superiority held across PD-L1 status and cisplatin eligibility. In patients who are cisplatin-eligible, EV + pembrolizumab significantly improved OS (HR: 0.68, 95%CI 0.47-0.99) and PFS (HR: 0.67, 95%CI 0.49-0.92) compared to nivolumab + chemotherapy. Durvalumab + tremelimumab was the safest combination for severe TRAEs, and EV + pembrolizumab ranked second. Our analyses support EV + pembrolizumab combination as a first-line treatment for locally advanced or metastatic UC. Thus, EV + pembrolizumab may become a guideline-changing standard treatment.
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a protokoly protinádorové kombinované chemoterapie $x terapeutické užití $x škodlivé účinky $7 D000971
- 650 12
- $a inhibitory kontrolních bodů $x terapeutické užití $7 D000082082
- 650 12
- $a síťová metaanalýza $7 D000071076
- 650 _2
- $a humanizované monoklonální protilátky $x terapeutické užití $x aplikace a dávkování $x škodlivé účinky $7 D061067
- 650 _2
- $a karcinom z přechodných buněk $x farmakoterapie $x mortalita $x patologie $7 D002295
- 650 _2
- $a urologické nádory $x farmakoterapie $x mortalita $x patologie $7 D014571
- 650 _2
- $a randomizované kontrolované studie jako téma $7 D016032
- 650 _2
- $a nádory močového měchýře $x farmakoterapie $x patologie $x mortalita $7 D001749
- 650 _2
- $a metastázy nádorů $7 D009362
- 650 _2
- $a monoklonální protilátky $7 D000911
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a systematický přehled $7 D000078182
- 655 _2
- $a metaanalýza $7 D017418
- 655 _2
- $a přehledy $7 D016454
- 700 1_
- $a Mori, Keiichiro $u Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Wahringer Gurtel 18-20, 1090, Vienna, Austria. morikeiichiro29@gmail.com $u Department of Urology, The Jikei University School of Medicine, Tokyo, Japan. morikeiichiro29@gmail.com
- 700 1_
- $a Matsukawa, Akihiro $u Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Wahringer Gurtel 18-20, 1090, Vienna, Austria $u Department of Urology, The Jikei University School of Medicine, Tokyo, Japan
- 700 1_
- $a Kawada, Tatsushi $u Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Wahringer Gurtel 18-20, 1090, Vienna, Austria $u Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan
- 700 1_
- $a Katayama, Satoshi $u Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Wahringer Gurtel 18-20, 1090, Vienna, Austria $u Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan
- 700 1_
- $a Laukhtina, Ekaterina $u Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Wahringer Gurtel 18-20, 1090, Vienna, Austria $u Institute for Urology and Reproductive Health, Sechenov University, Moscow, Russia
- 700 1_
- $a Rajwa, Pawel $u Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Wahringer Gurtel 18-20, 1090, Vienna, Austria $u Department of Urology, Medical University of Silesia, Zabrze, Poland
- 700 1_
- $a Quhal, Fahad $u Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Wahringer Gurtel 18-20, 1090, Vienna, Austria $u Department of Urology, King Fahad Specialist Hospital, Dammam, Saudi Arabia
- 700 1_
- $a Pradere, Benjamin $u Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Wahringer Gurtel 18-20, 1090, Vienna, Austria $u Department of Urology, La Croix Du Sud Hospital, Quint Fonsegrives, France
- 700 1_
- $a Fukuokaya, Wataru $u Department of Urology, The Jikei University School of Medicine, Tokyo, Japan
- 700 1_
- $a Iwatani, Kosuke $u Department of Urology, The Jikei University School of Medicine, Tokyo, Japan
- 700 1_
- $a Pichler, Renate $u Department of Urology, Comprehensive Cancer Center Innsbruck (CCCI), Medical University of Innsbruck, Innsbruck, Austria
- 700 1_
- $a Teoh, Jeremy Yuen-Chun $u S.H. Ho Urology Centre, Department of Surgery, The Chinese University of Hong Kong, Hong Kong, China
- 700 1_
- $a Moschini, Marco $u Department of Urology, San Raffaele Hospital and Scientific Institute, Milan, Italy
- 700 1_
- $a Krajewski, Wojciech $u Department of Minimally Invasive and Robotic Urology, Wrocław Medical University, Wrocław, Poland
- 700 1_
- $a Miki, Jun $u Department of Urology, The Jikei University School of Medicine, Tokyo, Japan
- 700 1_
- $a Shariat, Shahrokh F $u Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Wahringer Gurtel 18-20, 1090, Vienna, Austria $u Division of Urology, Department of Special Surgery, The University of Jordan, Amman, Jordan $u Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA $u Department of Urology, Second Faculty of Medicine, Charles University, Prague, Czech Republic $u Department of Urology, Weill Cornell Medical College, New York, NY, USA $u Karl Landsteiner Institute of Urology and Andrology, Vienna, Austria
- 700 1_
- $a Kimura, Takahiro $u Department of Urology, The Jikei University School of Medicine, Tokyo, Japan
- 710 2_
- $a European Association of Urology–Young Academic Urologists Urothelial Carcinoma Working Group (EAU-YAU)
- 773 0_
- $w MED00001041 $t Cancer immunology and immunotherapy $x 1432-0851 $g Roč. 74, č. 3 (2025), s. 76
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/39891702 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250415 $b ABA008
- 991 __
- $a 20250429134524 $b ABA008
- 999 __
- $a ok $b bmc $g 2311399 $s 1247089
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2025 $b 74 $c 3 $d 76 $e 20250201 $i 1432-0851 $m Cancer immunology and immunotherapy $n Cancer Immunol Immunother $x MED00001041
- LZP __
- $a Pubmed-20250415