Unique ID issued by UMIN | UMIN000011785 |
---|---|
Receipt number | R000013762 |
Scientific Title | Phase II randomized controlled trial of epirubicin hydrochloride and miriplatin hydrate as anticancer agents for transcatheter arterial chemoembolization of hepatocellular carcinoma |
Date of disclosure of the study information | 2013/09/20 |
Last modified on | 2025/03/03 13:13:11 |
Phase II randomized controlled trial of epirubicin hydrochloride and miriplatin
hydrate as anticancer agents for transcatheter arterial
chemoembolization of hepatocellular carcinoma
NHO-TGMC-2013-02 (HCC-Epirubicin &Miriplatin-P-II)
Phase II randomized controlled trial of epirubicin hydrochloride and miriplatin
hydrate as anticancer agents for transcatheter arterial
chemoembolization of hepatocellular carcinoma
NHO-TGMC-2013-02 (HCC-Epirubicin &Miriplatin-P-II)
Japan |
hepatocellular carcinoma
Hepato-biliary-pancreatic medicine | Hepato-biliary-pancreatic surgery |
Malignancy
NO
To compare the local control effects of transcatheter arterial chemoembolization
(TACE) using epirubicin with lipiodol and miriplatin with lipiodol for hepatocellular carcinoma, not indicated ressection nor ablation.
Safety
response rate
frequency of adverse events, changes of tumor markers, overall survival, one year survival rate, progression free survival
Interventional
Parallel
Randomized
Individual
Open -no one is blinded
Active
Numbered container method
2
Treatment
Medicine |
transcatheter arterial
chemoembolization for hepatocellular carcinoma by epirubicin
transcatheter arterial
chemoembolization for hepatocellular carcinoma by miriplatin
20 | years-old | <= |
Not applicable |
Male and Female
1) Histologically or clinically diagnosed hepatocellular carcinoma (HCC).
2) No previous history of TACE by epirubicin or miriplatin
3) No previous history of treatment with anticancer agents (neither by systemic nor arterial infusion)
4) No tyreatment effect expected by locoregional treatment.
5) Advanced HCC (BCLC stage-B or C).
6) Child-Pugh A or B.
7) Age of 20 years or more.
8) ECOG Performance Status of 0 or 1 or 2.
9) Existence of mesurable lesion by modified RECIST.
10) No major organ failure and all the laboratory data, below are conserved.
11) At least 3 months survival expected.
12) Written informed consent obtained from the patient.
1) Drug allergy by miriplatin or epirubicin.
2) Extrahepatic metastasis.
3) Portal venous invasion in the major trunk or first order branch.
4) Remarkable arterio-portal or arterio-venous shunting.
5) Hepatic artery occlusion.
6) Biliary reconstruction.
7) Comorbid diseases
*Cardiac failure
*Renal failure
*Active infection
*Active gastrointestinal bleeding
*Active associated cancers
*Hepatic encephalopathy
*Refractory ascites or pleural effusion
8) Fever (more than 38 degrees Celsius)
9) Allergy to contrast media
10) Pregnant or lactating
11) Other reasons not indicated to this study judged by doctors.
60
1st name | |
Middle name | |
Last name | Atsushi Naganuma |
Takasaki General Medical Center, National Hospital Organization
Department of Gastroenterology
36 Takamatsu-machi, Takasaki city, Gunma, Japan
027-322-5901
numackey@pa2.so-net.ne.jp
1st name | |
Middle name | |
Last name | Miyuki Toma |
Takasaki General Medical Center, National Hospital Organization
Clinical Research Department
36 Takamatsu-machi, Takasaki city, Gunma, Japan
027-322-5901
tcr-jimu3@takasaki-hosp.jp
Takasaki General Medical Center, National Hospital Organization
Takasaki General Medical Center, National Hospital Organization
NO
国立病院機構高崎総合医療センター
2013 | Year | 09 | Month | 20 | Day |
Unpublished
Completed
2013 | Year | 09 | Month | 19 | Day |
2023 | Year | 09 | Month | 19 | Day |
2013 | Year | 09 | Month | 20 | Day |
2025 | Year | 03 | Month | 03 | Day |
2025 | Year | 03 | Month | 03 | Day |
2013 | Year | 09 | Month | 17 | Day |
2025 | Year | 03 | Month | 03 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013762