Treatment strategies for locally advanced and metastatic urothelial carcinoma based on molecular profiles: A Review.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
환자: UC with FGFR3 mutations
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Although these novel therapies have demonstrated marked survival benefits for patients with locally advanced or metastatic UC, their efficacy can vary depending on the specific molecular profile present on cancer cells. In this review, we summarize the molecular classifications of UC and the corresponding treatment landscape associated with these classifications.
Urothelial carcinoma (UC), which includes bladder carcinoma (accounting for 90-95% of cases) and upper urinary tract carcinoma (comprising 5-10%), is one of the most prevalent malignancies worldwide.
APA
Hashimoto M, Fukiage K, et al. (2026). Treatment strategies for locally advanced and metastatic urothelial carcinoma based on molecular profiles: A Review.. Histology and histopathology, 41(4), 545-552. https://doi.org/10.14670/HH-18-972
MLA
Hashimoto M, et al.. "Treatment strategies for locally advanced and metastatic urothelial carcinoma based on molecular profiles: A Review.." Histology and histopathology, vol. 41, no. 4, 2026, pp. 545-552.
PMID
40762043
Abstract
Urothelial carcinoma (UC), which includes bladder carcinoma (accounting for 90-95% of cases) and upper urinary tract carcinoma (comprising 5-10%), is one of the most prevalent malignancies worldwide. For several decades, platinum-based chemotherapy has been the primary treatment modality for this disease. However, recent advancements have significantly transformed the therapeutic landscape for patients with UC. This transformation has been facilitated by the introduction of various treatment options, including immune checkpoint inhibitors targeting PD-L1 or PD-1, antibody-drug conjugates that target nectin-4 or trophoblast cell surface antigen 2 expressed on cancer cells, and fibroblast growth factor receptor (FGFR) inhibitors specifically indicated for Patients with UC with FGFR3 mutations. Although these novel therapies have demonstrated marked survival benefits for patients with locally advanced or metastatic UC, their efficacy can vary depending on the specific molecular profile present on cancer cells. In this review, we summarize the molecular classifications of UC and the corresponding treatment landscape associated with these classifications.
MeSH Terms
Humans; Carcinoma, Transitional Cell; Urinary Bladder Neoplasms; Urologic Neoplasms; Molecular Targeted Therapy; Biomarkers, Tumor; Immune Checkpoint Inhibitors
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