celecoxib has been researched along with Carcinoma, Transitional Cell in 11 studies
Carcinoma, Transitional Cell: A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS.
Excerpt | Relevance | Reference |
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" In these studies, we evaluated the COX-2 inhibitor celecoxib in two rodent models of urinary bladder cancer." | 7.70 | Celecoxib inhibits N-butyl-N-(4-hydroxybutyl)-nitrosamine-induced urinary bladder cancers in male B6D2F1 mice and female Fischer-344 rats. ( Grubbs, CJ; Hill, DL; Kelloff, GJ; Koki, AT; Leahy, KM; Lubet, RA; Masferrer, JL; Seibert, K; Steele, VE, 2000) |
"Celecoxib was not shown to reduce the risk of recurrence in intermediate- or high-risk non-muscle-invasive bladder cancer (NMIBC), although celecoxib was associated with delayed time to recurrence in pT1 NMIBC patients." | 5.30 | BOXIT-A Randomised Phase III Placebo-controlled Trial Evaluating the Addition of Celecoxib to Standard Treatment of Transitional Cell Carcinoma of the Bladder (CRUK/07/004). ( Andrews, S; Blazeby, J; Bogle, R; Brough, R; Burnett, S; Cresswell, J; Cruickshank, C; Hall, E; Huddart, R; Johnson, M; Kelly, JD; Madaan, S; Maynard, L; Mostafid, H; Palmer, A; Porta, N; Protheroe, A; Tan, WS, 2019) |
" We hypothesised that a combination of the cyclooxygenase 2 (COX-2) selective inhibitor celecoxib and intravesical bacillus Calmette-Guérin (BCG), an effective tumour immunoprophylaxis and ablative therapy for non-muscle-invasive bladder cancer, would be more effective than BCG alone." | 3.74 | Celecoxib has potent antitumour effects as a single agent and in combination with BCG immunotherapy in a model of urothelial cell carcinoma. ( Davies, BR; Dovedi, SJ; Kelly, JD; Kirby, JA; Leung, H, 2008) |
" In these studies, we evaluated the COX-2 inhibitor celecoxib in two rodent models of urinary bladder cancer." | 3.70 | Celecoxib inhibits N-butyl-N-(4-hydroxybutyl)-nitrosamine-induced urinary bladder cancers in male B6D2F1 mice and female Fischer-344 rats. ( Grubbs, CJ; Hill, DL; Kelloff, GJ; Koki, AT; Leahy, KM; Lubet, RA; Masferrer, JL; Seibert, K; Steele, VE, 2000) |
"Celecoxib was also administered via the diet to allow for systemic delivery of the drug." | 1.37 | Preclinical evaluation of a gene therapy treatment for transitional cell carcinoma. ( Godbey, WT; Zhang, X, 2011) |
"The human bladder cancer cell lines UM-UC-1, -3, and -6 were assayed for COX-2 expression by Western analysis using a monoclonal antibody to COX-2." | 1.33 | Selective cyclooxygenase-2 inhibitors inhibit growth and induce apoptosis of bladder cancer. ( Fischer, SM; Gee, J; Grossman, HB; Jendiroba, D; Lee, IL; Sabichi, AL, 2006) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 5 (45.45) | 29.6817 |
2010's | 6 (54.55) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Kelly, JD | 2 |
Tan, WS | 1 |
Porta, N | 1 |
Mostafid, H | 1 |
Huddart, R | 1 |
Protheroe, A | 1 |
Bogle, R | 1 |
Blazeby, J | 1 |
Palmer, A | 1 |
Cresswell, J | 1 |
Johnson, M | 1 |
Brough, R | 1 |
Madaan, S | 1 |
Andrews, S | 1 |
Cruickshank, C | 1 |
Burnett, S | 1 |
Maynard, L | 1 |
Hall, E | 1 |
Gore, JL | 1 |
Wright, JL | 1 |
Goldstein, MR | 1 |
Mascitelli, L | 1 |
Huang, KH | 1 |
Kuo, KL | 1 |
Ho, IL | 1 |
Chang, HC | 1 |
Chuang, YT | 1 |
Lin, WC | 1 |
Lee, PY | 1 |
Chang, SC | 1 |
Chiang, CK | 1 |
Pu, YS | 1 |
Chou, CT | 1 |
Hsu, CH | 1 |
Liu, SH | 1 |
Dhawan, D | 2 |
Craig, BA | 1 |
Cheng, L | 1 |
Snyder, PW | 1 |
Mohammed, SI | 1 |
Stewart, JC | 2 |
Zheng, R | 2 |
Loman, RA | 1 |
Foster, RS | 1 |
Knapp, DW | 2 |
Zhang, X | 1 |
Godbey, WT | 1 |
Gee, J | 1 |
Lee, IL | 1 |
Jendiroba, D | 1 |
Fischer, SM | 1 |
Grossman, HB | 1 |
Sabichi, AL | 1 |
Dovedi, SJ | 1 |
Kirby, JA | 1 |
Davies, BR | 1 |
Leung, H | 1 |
Brandau, S | 1 |
Jeffreys, AB | 1 |
Grubbs, CJ | 1 |
Lubet, RA | 1 |
Koki, AT | 1 |
Leahy, KM | 1 |
Masferrer, JL | 1 |
Steele, VE | 1 |
Kelloff, GJ | 1 |
Hill, DL | 1 |
Seibert, K | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
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Celecoxib for the Treatment of Non-muscle Invasive Bladder Cancer[NCT02343614] | Phase 2 | 58 participants (Actual) | Interventional | 2003-03-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
2 trials available for celecoxib and Carcinoma, Transitional Cell
Article | Year |
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BOXIT-A Randomised Phase III Placebo-controlled Trial Evaluating the Addition of Celecoxib to Standard Treatment of Transitional Cell Carcinoma of the Bladder (CRUK/07/004).
Topics: Administration, Intravesical; Aged; Antibiotics, Antineoplastic; Antineoplastic Combined Chemotherap | 2019 |
Effects of short-term celecoxib treatment in patients with invasive transitional cell carcinoma of the urinary bladder.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Carcinoma, Transitio | 2010 |
9 other studies available for celecoxib and Carcinoma, Transitional Cell
Article | Year |
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Can We Prevent Bladder Cancer Recurrences?
Topics: Carcinoma, Transitional Cell; Celecoxib; Humans; Neoplasm Recurrence, Local; Urinary Bladder Neoplas | 2019 |
Re: John L. Gore, Jonathan L. Wright. Can We Prevent Bladder Cancer Recurrences? Eur Urol 2019;75:602-3.
Topics: Carcinoma, Transitional Cell; Celecoxib; Humans; Neoplasm Recurrence, Local; Urinary Bladder Neoplas | 2019 |
Celecoxib-induced cytotoxic effect is potentiated by inhibition of autophagy in human urothelial carcinoma cells.
Topics: Adenine; Antineoplastic Agents; Autophagy; Autophagy-Related Protein 7; Carcinoma, Transitional Cell | 2013 |
Preclinical evaluation of a gene therapy treatment for transitional cell carcinoma.
Topics: Animals; BCG Vaccine; Carcinoma, Transitional Cell; Caspase 3; Caspase 9; Celecoxib; Cell Line, Tumo | 2011 |
Selective cyclooxygenase-2 inhibitors inhibit growth and induce apoptosis of bladder cancer.
Topics: Apoptosis; Blotting, Western; Carcinoma, Transitional Cell; Celecoxib; Cell Line, Tumor; Cell Prolif | 2006 |
Celecoxib has potent antitumour effects as a single agent and in combination with BCG immunotherapy in a model of urothelial cell carcinoma.
Topics: Analysis of Variance; Animals; BCG Vaccine; Blotting, Western; Carcinoma, Transitional Cell; Celecox | 2008 |
Editorial comment on: celecoxib has potent antitumour effects as a single agent and in combination with BCG immunotherapy in a model of urothelial cell carcinoma.
Topics: Animals; BCG Vaccine; Carcinoma, Transitional Cell; Celecoxib; Cyclooxygenase Inhibitors; Dinoprosto | 2008 |
Cyclooxygenase-2 dependent and independent antitumor effects induced by celecoxib in urinary bladder cancer cells.
Topics: Apoptosis; Blotting, Western; Carcinoma, Transitional Cell; Celecoxib; Cell Line, Tumor; Cell Prolif | 2008 |
Celecoxib inhibits N-butyl-N-(4-hydroxybutyl)-nitrosamine-induced urinary bladder cancers in male B6D2F1 mice and female Fischer-344 rats.
Topics: Animals; Anticarcinogenic Agents; Butylhydroxybutylnitrosamine; Carcinogens; Carcinoma, Squamous Cel | 2000 |