scholarly journals Clinical and Immunologic Results of a Phase II Trial of Sequential Imiquimod and Photodynamic Therapy for Vulval Intraepithelial Neoplasia

2008 ◽  
Vol 14 (16) ◽  
pp. 5292-5299 ◽  
Author(s):  
Ursula Winters ◽  
Sai Daayana ◽  
John T. Lear ◽  
Anne E. Tomlinson ◽  
Eyad Elkord ◽  
...  
2010 ◽  
Vol 102 (7) ◽  
pp. 1129-1136 ◽  
Author(s):  
S Daayana ◽  
E Elkord ◽  
U Winters ◽  
M Pawlita ◽  
R Roden ◽  
...  

2001 ◽  
Vol 8 (1) ◽  
pp. 65-71 ◽  
Author(s):  
Samantha K. Hendren ◽  
Stephen M. Hahn ◽  
Francis R. Spitz ◽  
Todd W. Bauer ◽  
Stephen C. Rubin ◽  
...  

2012 ◽  
Vol 30 (15_suppl) ◽  
pp. e14637-e14637
Author(s):  
Truls Hauge ◽  
Trond Warloe ◽  
Petra Weber Hauge ◽  
Isabel Franco-Lie ◽  
Anders Drolsum ◽  
...  

e14637 Background: Patients whocannot be offered curative surgical treatment for biliary tract cancer (BTC) have a poor prognosis. Photodynamic therapy (PDT) has been shown to improve survival and quality of life in patients with unresectable BTC. A combination of treatment modalities might improve survival further, but such data are still lacking. Therefore we have performed the first randomized trial on the combination of temoporfin/PDT and chemotherapy. Here we report data on the feasibility and safety. Methods: Randomized phase II trial, planned to include 20 patients with time to progression as primary endpoint, feasibility and toxicity as secondary endpoints. Inclusion criteria were unresectable BTC confirmed by histology or cytology, need for biliary stent, bilirubin level < 50 mmol/L and no previous cancer disease. The treatment arms were: A: Stent, temoporfin / PDT followed by gemcitabin / capecitabin (GemCap). B: Stent, GemCap. Only one initial PDT treatment was given. Results: Twenty patients with locally advanced and metastatic disease were included, 10 patients in each arm. Two patients in arm B did not receive any treatment (thrombocytopenia, study withdrawal) and two patients in arm A did not receive chemotherapy (ECOG>2, infection). PDT was feasible in all 10 patients without any acute procedure-related complication. During the first 30 days, two cases of cholangitis in arm A and three in arm B were observed. Cutaneous erythema (grade 1-2) was observed after PDT in two patients. Conclusions: PDT using temoporfin in combination with chemotherapy in BTC was feasible. Restrictions to light exposure were well tolerated. PDT in combination with chemotherapy did not increase the complication rate during the first 30 days follow-up. Three months follow-up data will be available at the time for presentation. Larger prospective trials are warranted to assess the efficacy of this treatment combination.


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