Intraluminal Brachytherapy in Unresectable Extrahepatic Biliary Duct Cancer: An Italian Pooled Analysis

2020 ◽  
Vol 40 (6) ◽  
pp. 3417-3421
Author(s):  
ROSA AUTORINO ◽  
SILVIA BISIELLO ◽  
BRIGIDA PAPPALARDI ◽  
VANESSA PRIVITERA ◽  
MILLY BUWENGE ◽  
...  
Author(s):  
Yoshitaka ENOMOTO ◽  
Atsushi KOGURE ◽  
Rika SAKAI ◽  
Shigeki TSUKAMOTO ◽  
Yoshimichi NAKAJIMA ◽  
...  
Keyword(s):  

2006 ◽  
Vol 17 (2) ◽  
pp. 135-135
Author(s):  
M Alimagham ◽  
S Aminiafshar ◽  
SMM H Moghaddam ◽  
S Shokuhi

Two cases of miliary tuberculosis and elevated levels of cancer antigen 125 Ovarian carcinoma is one of the most dangerous malignancies in women. The serum level of cancer antigen (CA) 125, as a tumour marker, is useful in the diagnosis of ovarian cancer. CA 125 serum level is also elevated in ascites (1), ovarian tube abscess (2,3), biliary duct cancer and periampullary tumours (4), cholangitis (5), cancer of pancreas (6) and cervical adenocarcinoma (7). Additionally, sometimes the serum level of CA 125 increases spontaneously during the menstrual cycle (8,9). In bone marrow transplantation, this marker is a sensitive index in the diagnosis of veno-occlusive disease (10). We describe an elevated serum level of CA 125 in two cases of tuberculosis (TB): one with cryptogenic miliary TB, and the other with miliary TB and meningitis.


2020 ◽  
Vol 40 ◽  
pp. 554
Author(s):  
H.M. Alvarez del Castillo Salazar ◽  
M.G. Serna-Thomé ◽  
G.D. Leal González ◽  
A.E. Padilla-Rosciano

HPB ◽  
2019 ◽  
Vol 21 ◽  
pp. S328-S329
Author(s):  
Keisuke Okamura ◽  
Satoshi Hirano ◽  
Takehiro Noji ◽  
Yoshinobu Nakanishi
Keyword(s):  

2017 ◽  
Vol 35 (15_suppl) ◽  
pp. e15661-e15661
Author(s):  
Angela Tatiana Alistar ◽  
Boris Pasche ◽  
Bonny Morris ◽  
Rodwige Desnoyer ◽  
Ralph D'Agostino

e15661 Background: Biliary duct carcinoma is a rare but highly fatal malignancy. The five-year survival rate for advanced bile duct cancer is 2%, per SEER data. As such, new treatment options are desperately needed. CPI-613, a novel anticancer agent that selectively inhibits mitochondrial metabolism in cancer cells, was employed in this study. Methods: This phase 1 study utilized a two-stage dose-escalation schema to determine the maximum-tolerated dose (MTD) and safety of single agent CPI-613 in patients with locally advanced or metastatic bile duct cancers. The 1st cohort enrolled 4 patients at 2300 mg/m2, with no dose-limiting toxicities (DLT) observed. The 2nd cohort enrolled patients at 1200 mg/m2/day for pre-cycle (days 1-5) and 3000 mg/m2 on days 1 and 4 weekly for 3 weeks (28 day cycle). The 5th and 6th patient experienced a DLT. The 3rd cohort was initiated at 600 mg/m2 pre-cycle and 3000 mg/m2 weekly with no other DLTs observed. Results: To-date, 14 patients have been enrolled in the study. The MTD was determined at 600 mg/m2/day pre-cycle and 3000 mg/m2 as per schedule. Once the MTD was determined, the cohort was expanded and, 8 patients have been treated at the MTD with no DLTs observed. Two additional patients are planned to be enrolled at this dose prior to trial completion. Of these 8 patients, 3 are still alive with 1 having prolonged survival (15 months) and the other 2 still on treatment. The most commonly observed toxicities were mild, such as anemia, anorexia, dehydration, fatigue, nausea and thrombocytopenia. Conclusions: Treatment with CPI-613 was well tolerated by patients with heavy tumor burden and refractory disease. CPI-613 has recently been shown to be well tolerated in combination with FOLFIRINOX in pancreatic cancer patients. Due to the low toxicity of CPI-613 in this study, even among highly symptomatic patients, it is anticipated that combination with other active agents is feasible in patients with advanced bile duct cancer. CPI-613 represents a novel treatment that could prove to be an exciting therapeutic alternative for patients with previously limited options and poor survival. Clinical trial information: NCT01766219.


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