UMIN-CTR Clinical Trial

Recruitment status Main results already published
Unique ID issued by UMIN C000000271
Receipt No. R000000342
Official scientific title of the study A phase II study of cisplatin with TS-1 for patients with cancer of primary unknown
Date of disclosure of the study information 2005/10/31
Last modified on 2018/03/04 (Ver. 9)

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Basic information
Official scientific title of the study A phase II study of cisplatin with TS-1 for patients with cancer of primary unknown
Title of the study (Brief title) A phase II study of cisplatin with TS-1
Region
Japan

Condition
Condition cancer of primary unknown
Classification by specialty
Hematology and clinical oncology
Classification by malignancy Malignancy
Genomic information NO

Objectives
Narrative objectives1 To investigate the effect of cisplatin with TS-1 for patients for patients with cancer of primary unknown
Basic objectives2 Safety
Basic objectives -Others
Trial characteristics_1 Exploratory
Trial characteristics_2
Developmental phase Phase II

Assessment
Primary outcomes Response Rate
Key secondary outcomes Safety Profile

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 Chemotherapy
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
99 years-old >=
Gender Male and Female
Key inclusion criteria The eligibility criteria are as follows;(1) histologic or cytologic confirmation of metastatic cancer with unknown primary site
(2) not subject to radiation or surgery(3) measurable or evaluable lesions;
(4) no previous treatments
(5) Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-2
(6)age more than 20
(7) adequate organ function
(8) written informed consent
Key exclusion criteria The exclusion criteria are as follows:
1.female adenocarcinoma with axillary lymph nodes swelling only, or pelvic cavity endolymph nodes only
2.squamous carcinoma with cervical lymph nodes swelling only, or inguen lymph nodes only
3.patients with germ cell tumor or have characteristic of neuroendocrine tumor
4.patients with high level of PSA in serum or tumor
(1) severe infection or other severe complications (such as gastrointestinal bleeding, heart disease)
(2) symptomatic brain metastasis
(3) patients who carried out bone marrow transplantation
(4) patients who carried out peripheral blood stem cell transplantation
(5) drug allergy
(6) pregnancy or lactating
(7) male patients who hope for pregnancy
(8) uncontrollable diabetes mellitus
Target sample size 45

Research contact person
Name of lead principal investigator Takayasu Kurata
Organization Kinki University School of Medicine
Division name Department of Medical Oncology
Address 377-2, Ohno-Higashi, Osakasayama, Osaka
TEL 072-366-0221
Email kuratat@hirakata.kmu.ac.jp

Public contact
Name of contact person Takayasu Kurata
Organization Kinki University School of Medicine
Division name Department of Medical Oncology
Address 377-2, Ohno-Higashi, Osakasayama, Osaka
TEL 072-366-0221
Homepage URL
Email t-kurata@med.kindai.ac.jp

Sponsor
Institute Department of Medical Oncology, Kinki University School of Medicine
Institute
Department

Funding Source
Organization Department of Medical Oncology, Kinki University School of Medicine
Organization
Division
Category of Funding Organization Self funding
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

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

Other administrative information
Date of disclosure of the study information
2005 Year 10 Month 31 Day

Progress
Recruitment status Main results already published
Date of protocol fixation
2005 Year 10 Month 01 Day
Anticipated trial start date
2005 Year 10 Month 01 Day
Last follow-up date
2010 Year 09 Month 01 Day
Date of closure to data entry
2011 Year 12 Month 01 Day
Date trial data considered complete
2011 Year 12 Month 01 Day
Date analysis concluded
2011 Year 12 Month 01 Day

Related information
URL releasing protocol
Publication of results Published
URL releasing results
Results
Other related information

Management information
Registered date
2005 Year 10 Month 31 Day
Last modified on
2018 Year 03 Month 04 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000000342