A Phase II Study of Cisplatin in Patients with Biliary Tract Carcinoma

Oncology ◽  
1994 ◽  
Vol 51 (6) ◽  
pp. 515-517 ◽  
Author(s):  
Shuichi Okada ◽  
Hiroshi Ishii ◽  
Haruhiko Nose ◽  
Masayoshi Yoshimori ◽  
Takuji Okusaka ◽  
...  
2020 ◽  
Vol 40 (2) ◽  
pp. 929-938 ◽  
Author(s):  
JOSEPH SGOUROS ◽  
GERASIMOS ARAVANTINOS ◽  
GEORGIA-ANGELIKI KOLIOU ◽  
GEORGE PENTHEROUDAKIS ◽  
FLORA ZAGOURI ◽  
...  

Hepatology ◽  
2015 ◽  
Vol 62 (5) ◽  
pp. 1456-1465 ◽  
Author(s):  
Andrej Wagner ◽  
Ulrike W. Denzer ◽  
Daniel Neureiter ◽  
Tobias Kiesslich ◽  
Andreas Puespoeck ◽  
...  

BMC Cancer ◽  
2006 ◽  
Vol 6 (1) ◽  
Author(s):  
Kazuma Kobayashi ◽  
Akihito Tsuji ◽  
Sojiro Morita ◽  
Tadashi Horimi ◽  
Tetsuhiko Shirasaka ◽  
...  

2011 ◽  
Vol 29 (15_suppl) ◽  
pp. e14653-e14653 ◽  
Author(s):  
J. Yi ◽  
S. Thongprasert ◽  
D. Doval ◽  
J. Lee ◽  
M. N. Cho ◽  
...  

2020 ◽  
Vol 38 (15_suppl) ◽  
pp. e16684-e16684
Author(s):  
Chenchen Wang ◽  
Weijian Guo ◽  
Mingzhu Huang

e16684 Background: There is no standard second-line therapy for advanced biliary tract carcinoma (BTC). Apatinib, a VEGFR2 tyrosine kynase inhibitor, showed an inhibitary effect on tumor formation in BTC tumorgraft mouse model in previous study, with tolerable toxicity in clinical trials for other types of advanced cancer such as gastric cancer. We conducted an exploratory study to evaluate the efficacy and safety of apatinib in patients with advanced BTC. Methods: This is a single-center, single-arm phase II study (NCT03427242). The key inclusion criteria were:(1) histologically confirmed advanced or metastatic BTC; (2) Prior lack of response or intolerance to at least one chemotherapeutic regimens; (3) At least one measurable lesion as defined by RECIST 1.1; (4) No prior use of anti-angiogenic targeted drugs. Eligible patients received oral apatinib 500mg each day continuously until unacceptable toxicity or tumor progression. The primary endpoint was progression free survival (PFS). The secondary endpoints were overall survival (OS), objective response rate (ORR), disease control rate (DCR) and treatment safety. Results: From Dec 1, 2017 to Jan 31, 2020, a total of 18 patients (12 males and 6 females) had been recruited, and 16 patients who had received the medication of apatinib were included in this analysis. Among these patients, 10 were previously treated with only first-line chemotherapy and 6 were treated with two or more lines of therapy. The median age was 65 (range 45-76) years old. Fourteen patients had received the efficacy evaluation after treatment. Two patients achieved partial response (PR, 14.3%), 6 patients with stable disease (SD, 42.9%),and 6 patients with progressive disease(PD). The ORR and DCR were 14.3% and 57.1%, respectively. At the last follow-up date on Jan 30, 2020, 4 patients are still on apatinib medication. The median PFS was 2.70 months (95% CI, 1.94 - 3.46), and the median OS was 7.03 months (95% CI, 3.16 - 10.9). Grade 3 or 4 adverse events were reported in 7 patients (43.8%). The detailed grade 3 or 4 adverse events were proteinuria in 5 patients, hand-foot syndrome in 2 patients, platelet count decrease in 1 patients, diarrhea in 1 patients and urine bilirubin in 1 patients (Table). Conclusions: For the patients with advanced biliary tract carcinoma, apatinib showed an anti-tumor activity with acceptable safety. Clinical trial information: NCT03427242 . [Table: see text]


2012 ◽  
Vol 48 (2) ◽  
pp. 196-201 ◽  
Author(s):  
Jun Ho Yi ◽  
Sumitra Thongprasert ◽  
Jeeyun Lee ◽  
D.C. Doval ◽  
Se Hoon Park ◽  
...  

2021 ◽  
Vol 13 ◽  
pp. 175883592110390
Author(s):  
Chenchen Wang ◽  
Mingzhu Huang ◽  
Qirong Geng ◽  
Wenhua Li ◽  
Jinjia Chang ◽  
...  

Background: There is no standard therapy for metastatic biliary tract carcinoma (BTC) refractory to first-line chemotherapy. Apatinib, a VEGFR2 tyrosine kynase inhibitor, showed an activity against BTC xenografts in preclinical models. We conducted an exploratory study to evaluate the efficacy and safety of apatinib in patients with metastatic BTC. Methods: This is a single-arm phase II study [ClinicalTrials.gov identifier: NCT03427242]. Eligible patients were aged 18 years or older; histologically confirmed metastatic BTC; refractory or intolerance to at least one chemotherapeutic regimen; no prior use of anti-angiogenic targeted drugs; Eastern Cooperative Oncology Group performance status of 0–2. Patients received oral apatinib 500 mg each day continuously until unacceptable toxicity or tumor progression. The primary endpoint was progress free survival (PFS). The secondary endpoint was overall survival (OS), objective response rate (ORR) and treatment safety. Results: A total of 22 patients were recruited. All of them received apatinib medication. The median age was 63 (44–75) years old. Twenty patients received efficacy evaluation after treatment. The objective response rate (ORR) and disease control rate (DCR) were 15.0% and 60.0%, respectively. The median PFS was 2.73 months [95% confidence interval (CI): 1.74–3.72 months], with 6 months PFS rate of 27.3% (95% CI: 8.7–45.9%). The median OS was 4.81 months (95% CI: 3.16–10.9 months), with 12 months OS rate of 36.4% (95% CI: 16.2–56.6%). Nine out of 22 patients (40.9%) had grade 3/4 adverse events. The most common grade 3/4 adverse events were hand-foot skin syndrome [three (13.6%) patients] and hypertension [two (9.1%) patients]. No treatment-related death occurred. Conclusions: For patients with metastatic BTC, apatinib showed an anti-tumor activity with acceptable safety, which deserves the further clinical trial. This trial was prospectively registered on ClinicalTrials.gov [NCT03427242]. Date of first patient enrollment: 26 January 2018. Date of registration (date of first posted): 9 February 2018.


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