UMIN-CTR Clinical Trial

Basic information
Official scientific title of the study	Prospective cohort study of neoadjuvant chemotherapy using tri-weekly carboplatin and weekly paclitaxel for patients with locally advanced cervical cancer
Title of the study (Brief title)	CC-NAC
Region	Japan

Condition
Condition	cervical cancer
Classification by specialty	Obsterics and gynecology
Classification by malignancy	Malignancy
Genomic information	NO

Objectives
Narrative objectives1	To assess the efficacy and safety of neoadjuvant chemotherapy using tri-weekly carboplatin and weekly paclitaxel in patients with locally advanced cervical cancer.
Basic objectives2	Others
Basic objectives -Others	To construct pathological mapping of residual tumor after neoadjuvant chemotherapy.
Trial characteristics_1	Exploratory
Trial characteristics_2	Explanatory
Developmental phase	Not applicable

Assessment
Primary outcomes	2 year recurrence free survival rate
Key secondary outcomes	Response rate, Pathological CR rate, 2 year overall survival rate, Toxicity, Site of recurrence, Completion rate of the neoadjuvant chemotherapy

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	Neoadjuvant chemotherapy (3 cycles of dose dense TC therapy)
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	Female
Key inclusion criteria	1. Histologically proven cervical cancer. 2. FIGO stage Ib2, IIa2, IIb. 3. ECOG Performance Status: 0 to 2.
Key exclusion criteria	1. Previous chemotherapy. 2. Concomitant malignancy. 3. Severe complication.
Target sample size	100

Research contact person
Name of lead principal investigator	Shoji Nago
Organization	Hyogo Cancer Center
Division name	Gynecologic Oncology
Address	13-70Kitaoji-cho, Akashi-city
TEL	078-929-1151
Email	nagao@hp.pref.hyogo.jp

Public contact
Name of contact person	Shoji Nagao
Organization	Hyogo Cancer Center
Division name	Gynecologic Oncology
Address	13-70Kitaoji-cho, Akashi-city
TEL	078-929-1151
Homepage URL
Email	nagao@hp.pref.hyogo.jp

Sponsor
Institute	Hyogo Cancer CEnter
Institute
Department

Funding Source
Organization	Hyogo Cancer Center
Organization
Division
Category of Funding Organization	Local Government
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	兵庫県立がんセンター

Other administrative information
Date of disclosure of the study information	2016 Year 10 Month 01 Day

Progress
Recruitment status	Open public recruiting
Date of protocol fixation	2016 Year 09 Month 14 Day
Anticipated trial start date	2016 Year 09 Month 23 Day
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

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

Management information
Registered date	2016 Year 09 Month 23 Day
Last modified on	2016 Year 09 Month 23 Day

Link to view the page
URL(English)	https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000027792