Clinical utility of checkpoint inhibitors against metastatic bladder cancer: overcoming challenges to find a way forward

被引:6
作者
Bile-Silva, Andreia [1 ]
Lopez-Beltran, Antonio [2 ]
Blanca, Ana [3 ]
Lopez-Rios, Fernando [4 ]
Gomez-Gomez, Enrique [3 ]
Cimadamore, Alessia [5 ]
Montironi, Rodolfo [6 ]
Vau, Nuno [7 ]
Cheng, Liang [8 ]
机构
[1] Ctr Hosp Lisboa Ocidental, Egas Moniz Hosp, Urol Dept, Lisbon, Portugal
[2] Cordoba Univ, Dept Morphol Sci, Unit Pathol, Med Sch, Cordoba, Spain
[3] Reina Sofia Univ Hosp, Urol Dept, Cordoba, Spain
[4] Univ Complutense Madrid, 12 Octubre Univ Hosp, Res Inst 12 Octubre Univ Hosp I 12, Pathol Dept, Madrid, Spain
[5] Univ Udine, Inst Pathol Anat, Dept Med Area DAME, Udine, Italy
[6] Polytech Univ Marche, Mol Med & Cell Therapy Fdn, Ancona, Italy
[7] Champalimaud Clin Ctr, Med Oncol, Lisbon, Portugal
[8] Brown Univ, Warren Alpert Med Sch, Dept Pathol & Lab Med, Providence, RI USA
关键词
Bladder cancer; immune checkpoint inhibitor; immunotherapy; PD-1; PD-L1; biomarkers; TMB; ctDNA; CISPLATIN-INELIGIBLE PATIENTS; UROTHELIAL CARCINOMA; OPEN-LABEL; SINGLE-ARM; GENE-EXPRESSION; LONG-TERM; CHEMOTHERAPY; MULTICENTER; ATEZOLIZUMAB; THERAPY;
D O I
10.1080/14712598.2023.2201371
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Cisplatin-based chemotherapy is currently considered the gold-standard treatment for metastatic urothelial carcinoma (mUC). Nevertheless, most mUC patients develop resistance to chemotherapy. Immune checkpoint inhibitors (ICI) have emerged as a therapeutic option for mUC. ICI are used as both first- and second-line therapy for patients with mUC but also for maintenance following chemotherapy and durable responses may be expected in these settings.Areas covered: Patients with mUC who experience progression after platinum-based chemotherapy regimens, those who are cisplatin-ineligible and have positive PD-L1 expression, and those who are platinum-ineligible, regardless of PD-L1 status, are the target population. The role of ICI monotherapy or drug combinations and newer proposals for mUC therapy are reviewed. The current status of biomarkers to guide ICI treatments in mUC is also provided, focusing on PD-L1, tumor mutational load, and liquid biopsies using ctDNA.Expert opinion: Current challenges to improve the role of ICI in mUC could be summarized as i) development of better drugs; ii) advances in drug-combinations schemes; iii) development of novel biomarkers and techniques to better select patients for this treatment; iv) providing the drugs in the optimal clinical setting; v) promoting trials covering more demographic and clinical heterogeneity (i.e. wider age range, gender, and diverse clinical representation).
引用
收藏
页码:407 / 418
页数:12
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