2017
DOI: 10.1016/j.urolonc.2017.09.021
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Update of systemic immunotherapy for advanced urothelial carcinoma

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Cited by 12 publications
(7 citation statements)
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References 40 publications
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“…The 5‐y survival rate for all patients diagnosed with bladder cancer is 77%, but falls to 36% for those with disease that spreads to regional lymph nodes and to <5% for those with distant metastases 1 . Until recently, initial treatments for patients with metastatic UC have been limited to platinum‐based chemotherapy 2 . Median OS was reported as between 14.1 and 15.5 mo for patients who received cisplatin‐containing regimens 3,4 and 13.8 mo for patients who received carboplatin‐containing regimens 3 .…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…The 5‐y survival rate for all patients diagnosed with bladder cancer is 77%, but falls to 36% for those with disease that spreads to regional lymph nodes and to <5% for those with distant metastases 1 . Until recently, initial treatments for patients with metastatic UC have been limited to platinum‐based chemotherapy 2 . Median OS was reported as between 14.1 and 15.5 mo for patients who received cisplatin‐containing regimens 3,4 and 13.8 mo for patients who received carboplatin‐containing regimens 3 .…”
Section: Introductionmentioning
confidence: 99%
“…1 Until recently, initial treatments for patients with metastatic UC have been limited to platinum-based chemotherapy. 2 Median OS was reported as between 14.1 and 15.5 mo for patients who received cisplatin-containing regimens 3,4 and 13.8 mo for patients who received carboplatin-containing regimens. 3 For patients ineligible for cisplatin-containing regimens, median survival was only 8-9 mo with carboplatin-based combination chemotherapy.…”
Section: Introductionmentioning
confidence: 99%
“…Genomic profiling was also conducted for exploratory biomarker analysis using the FoundationOne panel (72). Treatment with atezolizumab resulted in improved survival, with higher levels of PD-L1 expression on immune cells, though not with tumor cells, or higher TMB associated with higher response rate (73,74). PD-L1 expression was then incorporated into FDA labeling in 2018 following the IMvigor210 clinical trial, to select patients who should receive Tecentriq treatment (74,75).…”
Section: Atezolizumab (Tecentriq)mentioning
confidence: 99%
“…Treatment with atezolizumab resulted in improved survival, with higher levels of PD-L1 expression on immune cells, though not with tumor cells, or higher TMB associated with higher response rate (73,74). PD-L1 expression was then incorporated into FDA labeling in 2018 following the IMvigor210 clinical trial, to select patients who should receive Tecentriq treatment (74,75). Tumor specimens were prospectively evaluated using the Ventana PD-L1 (SP142) assay and patients with high levels of PD-L1 expression had improved PR, CR, and ORR.…”
Section: Atezolizumab (Tecentriq)mentioning
confidence: 99%
“…Ингибиторы контрольных точек иммунитета являются первым новым классом препаратов, показавшим большую эффективность в 1-й линии терапии пациентов с метастатическим уротелиальным раком с противопоказанием к применению цисплатина и во 2-й линии у пациентов с прогрессированием заболевания на фоне ХТ на основе платины [5][6][7][8][9][10][11][12]. Комбинированные схемы, сочетающие ХТ на основе платины и ингибиторы PD-L1 и PD-1, привлекательны по нескольким причинам.…”
Section: Introductionunclassified