UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000008689
Receipt number R000008809
Scientific Title A clinical study on safety and efficacy of sorafenib as maintenance chemotherapy after percutaneous isolated hepatic perfusion chemotherapy (PIHP) for advanced hepatocellular carcinoma
Date of disclosure of the study information 2012/09/19
Last modified on 2018/02/17 21:21:32

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Basic information

Public title

A clinical study on safety and efficacy of sorafenib as maintenance chemotherapy after percutaneous isolated hepatic perfusion chemotherapy (PIHP) for advanced hepatocellular carcinoma

Acronym

A safety and efficacy of sorafenib as maintenance chemotherapy after percutaneous isolated hepatic perfusion (PIHP) for advanced hepatocellular carcinoma

Scientific Title

A clinical study on safety and efficacy of sorafenib as maintenance chemotherapy after percutaneous isolated hepatic perfusion chemotherapy (PIHP) for advanced hepatocellular carcinoma

Scientific Title:Acronym

A safety and efficacy of sorafenib as maintenance chemotherapy after percutaneous isolated hepatic perfusion (PIHP) for advanced hepatocellular carcinoma

Region

Japan


Condition

Condition

hepatocellular carcinoma

Classification by specialty

Hepato-biliary-pancreatic surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to analyze the safety and efficacy of sorafenib as maintenance therapy after percutaneous isolated hepatic perfusion (PIHP) for advanced hepatocellular carcinoma

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2


Developmental phase

Phase I,II


Assessment

Primary outcomes

One year overall survival

Key secondary outcomes

Progression or recurrence free survival
Overall survival
Safety of sorafenib administration after PIHP


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

After 4-8 weeks of PIHP, sorafenib therapy starts with a primary dose of 800mg/day. Sorafenib therapy continues until the appearance of unacceptable side effect or tumor progression.

Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1)Patients who underwent PIHP for advanced hepatocellular carcinoma
2)Patients who were diagnosed as hepatocellular carcinoma radiologically or pathologically
3)Patients who have no indication of surgical resection, local therapy (RFA, TACE, percutaneous ethanol injection)
4)Patients who satisfy the criteria of sorafenib administration
5)Patients who approve sorafenib therapy and sign a document for it.

Key exclusion criteria

1)Patients with a history of molecular- target therapy including sorafenib.
2)Patients with a history of hypersensitivity of sorafenib
3)Patients who are pregnant or on nurse.
4)Patients who are on dialysis
5)Patients with uncontrolled hypertension
6)Patients with a history of thrombosis, embolism, or ischemic Heart Disease
7)Patients with brain metastasis
8)Patients with esophageal varix with bleeding tendency
9)Patients with gastrointestinal bleeding within one month
10)Patients with ongoing or history of hepatic encephalopathy
11)Patients who undergo rifampin
12)Patients with HIV or AIDS
13)Patients with synclonous double cancer

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Fukumoto Takumi

Organization

Kobe University

Division name

Department of hepato-biliary-pancreatic surgery

Zip code


Address

7-5-2, Kusunokicho, Chuo-Ku, Kobe, Japan

TEL

078-382-6302

Email

fukumoto@med.kobe-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Motofumi Tanaka

Organization

Kobe University

Division name

Department of hepato-biliary-pancreatic surgery

Zip code


Address

7-5-2, Kusunokicho, Chuo-Ku, Kobe, Japan

TEL

078-382-6302

Homepage URL


Email

motofutanaka-gi@umin.net


Sponsor or person

Institute

Department of hepato-biliary-pancreatic surgery, Kobe University

Institute

Department

Personal name



Funding Source

Organization

Bayer Pharma

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

Kobe University Graduate School of Medicine


Other administrative information

Date of disclosure of the study information

2012 Year 09 Month 19 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2012 Year 08 Month 15 Day

Date of IRB


Anticipated trial start date

2012 Year 10 Month 01 Day

Last follow-up date

2017 Year 01 Month 19 Day

Date of closure to data entry


Date trial data considered complete

2017 Year 01 Month 19 Day

Date analysis concluded

2017 Year 01 Month 31 Day


Other

Other related information



Management information

Registered date

2012 Year 08 Month 15 Day

Last modified on

2018 Year 02 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000008809


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name