| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Fléchon, Aude |
| dc.contributor.author | ALVA, AJJAI |
| dc.contributor.author | Powles, Thomas |
| dc.contributor.author | ÖZGÜROGLU, MUSTAFA |
| dc.contributor.author | Csoszi, Tibor |
| dc.contributor.author | Morales-Barrera, Rafael |
| dc.date.accessioned | 2024-12-10T10:26:27Z |
| dc.date.available | 2024-12-10T10:26:27Z |
| dc.date.issued | 2024-12-01 |
| dc.identifier.citation | Fléchon A, Morales-Barrera R, Powles T, Alva A, Özgüroğlu M, Csöszi T, et al. Association of Tumor Mutational Burden and PD-L1 with the Efficacy of Pembrolizumab with or without Chemotherapy versus Chemotherapy in Advanced Urothelial Carcinoma. Clin Cancer Res. 2024 Dec 1;30(23):5353–64. |
| dc.identifier.issn | 1557-3265 |
| dc.identifier.uri | https://hdl.handle.net/11351/12317 |
| dc.description | Tumor mutational burden; Chemotherapy; Advanced urothelial carcinoma |
| dc.description.abstract | Purpose:
The three-arm, phase III KEYNOTE-361 study did not meet its dual primary endpoints of progression-free survival (PFS) or overall survival (OS) with first-line pembrolizumab plus chemotherapy versus chemotherapy in advanced urothelial carcinoma. This prespecified exploratory analysis assessed the association of tumor mutational burden (TMB) and PD-L1 combined positive score (CPS) with clinical outcomes.
Patients and Methods:
TMB and PD-L1 CPS were determined via whole-exome sequencing and PD-L1 IHC 22C3 pharmDx, respectively. The association was evaluated in each treatment arm using logistic regression [objective response rate (ORR)] and Cox proportional hazards regression models (PFS and OS); one-sided (pembrolizumab monotherapy; pembrolizumab plus chemotherapy) and two-sided (chemotherapy) nominal P values were calculated. Significance was prespecified at α = 0.05 without multiplicity adjustment. Efficacy was evaluated by prespecified cutoffs of 175 mutations/exome (TMB) and CPS 10 (PD-L1).
Results:
Of the 993 treated patients, 820 (82.6%) and 993 (100%) had evaluable TMB and CPS data, respectively. Continuous TMB was positively associated with ORR, PFS, and OS for pembrolizumab monotherapy (one-sided P < 0.001, P < 0.001, and P = 0.007, respectively); PFS and OS for pembrolizumab plus chemotherapy (one-sided P = 0.007 and P = 0.010, respectively); and OS for chemotherapy alone (two-sided P = 0.040). Continuous PD-L1 CPS showed evidence of anticipated association with ORR and PFS for pembrolizumab monotherapy. The subgroup with TMB ≥175 mutations/exome and PD-L1 CPS ≥10 had the highest PFS and OS improvements with pembrolizumab alone or with chemotherapy versus chemotherapy alone.
Conclusions:
These data suggest that TMB may be predictive of the response to pembrolizumab alone or with chemotherapy in advanced urothelial carcinoma. |
| dc.language.iso | eng |
| dc.publisher | American Association for Cancer Research |
| dc.relation.ispartofseries | Clinical Cancer Research;30(23) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Marcadors tumorals |
| dc.subject | Quimioteràpia combinada |
| dc.subject | Medicaments antineoplàstics - Ús terapèutic |
| dc.subject | Anticossos monoclonals - Ús terapèutic |
| dc.subject | Bufeta - Càncer - Aspectes genètics |
| dc.subject | Bufeta - Càncer - Tractament |
| dc.subject.mesh | Biomarkers, Tumor |
| dc.subject.mesh | Antibodies, Monoclonal, Humanized |
| dc.subject.mesh | Antineoplastic Agents, Immunological |
| dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols |
| dc.subject.mesh | Urologic Neoplasms |
| dc.title | Association of Tumor Mutational Burden and PD-L1 with the Efficacy of Pembrolizumab with or without Chemotherapy versus Chemotherapy in Advanced Urothelial Carcinoma |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1158/1078-0432.CCR-23-3518 |
| dc.subject.decs | marcadores tumorales |
| dc.subject.decs | anticuerpos monoclonales humanizados |
| dc.subject.decs | inmunoterapia antineoplásica |
| dc.subject.decs | protocolos de quimioterapia antineoplásica combinada |
| dc.subject.decs | neoplasias urológicas |
| dc.relation.publishversion | https://doi.org/10.1158/1078-0432.CCR-23-3518 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [Fléchon A] Department of Medical Oncology, Centre Léon Bérard, Lyon, France. [Morales-Barrera R] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [Powles T] Barts Cancer Centre, St Bartholomew’s Hospital, London, United Kingdom. Barts Cancer Institute, Barts Health NHS Trust, Queen Mary University of London, London, United Kingdom. [Alva A] University of Michigan Health System, Ann Arbor, Michigan. [Özgüroğlu M] Division of Medical Oncology, Department of Internal Medicine, Cerrahpasa School of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey. [Csöszi T] County Oncology Centre, Hetényi Géza Hospital, Szolnok, Hungary |
| dc.identifier.pmid | 39475359 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |