UMIN-CTR Clinical Trial

Basic information
Official scientific title of the study	Multicenter Phese II Study of Optimal-XELOX plus Bevacizumab Therapy with Oxaliplatin Stop-and-Go Strategy and Oral capecitabin plus Bevacizumab Maintenance Therapy in Advanced Colorectal Cancer
Title of the study (Brief title)	Phese II Study of Optimal-XELOX plus Bevacizumab Therapy in Advanced Colorectal Cancer (CCOG-0902 Study)
Region	Japan

Condition
Condition	Colorectal cancer
Classification by specialty	Gastroenterology Gastrointestinal surgery
Classification by malignancy	Malignancy
Genomic information	NO

Objectives
Narrative objectives1	To evaluate the efficacy and safety of optimal-XELOX plus bevacizumab therapy considering Oxaliplatin Stop-and-Go Strategy in Advanced Colorectal Cancer.
Basic objectives2	Safety,Efficacy
Basic objectives -Others
Trial characteristics_1	Exploratory
Trial characteristics_2	Pragmatic
Developmental phase	Phase II

Assessment
Primary outcomes	Progression free survival
Key secondary outcomes	Overall response rate, Overall survival, Duration of disease control, Reintroduction rate of XELOX+bavacizumab therapy, Safety

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	(1)Initial therapy : XELOX+bevacizumab therapy (2)Maintenance therapy : capecitabine+bevacizumab therapy (3)Reintroduced therapy : XELOX+bevacizumab 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	Male and Female
Key inclusion criteria	(1) Histopathologically confirmed colorectal cancer. (2) Written informed consent. (3) Age of 20 years or older. (4) ECOG performance status 0-1. (5) Life expectancy greater than 3 months. (6) Measurable or evaluable disease (RECIST ver.1.1.). (7) Untreated colorectal cancer. (8) Adequate organ function.
Key exclusion criteria	(1) Previous history of severe drug-induced allergy (2) Brain metastasis (3) Cerebrovascular disease or its symptoms within 1 year. (4) Massive pleural effusion or ascites that required drainage. (5) History of active double cancer. (6) Previous history of thoromboembolitic disease, or necessity for antithrombotic drug. (7) Intestinal bleeding, ileus, bowel obstruction or uncontrolled peptic ulcer. (8) History of gastrointestinal perforation within 1 year. (9) Diathesis of bleeding (history of hemoptysis, including cavitation and/or necrosis in lung metastasis confirmed by imaging), coagulopathy. (10) Severe renal failure or urinary protein (more than 2+). (11) Uncontrolled severe complications (DM, hypertension, diarrhea, et al.). (12) Patient with symptomatic cardiovascular disease or asymptomatic disease but have been treated (>=Grade 2 according to NCI-CTCAE ver.4). History of myocardial infarction within a year. (13) Interstitial lung disease or pulmonary fibrosis. (14) Uncontrolled infection. (15) Patient receiving surgical procedure or such as skin-open biopsy, trauma surgery, or other more intensive surgeries within 4 weeks or aspiration biopsy within a week. (16) Pregnant women, possibly pregnant women, wishing to become pregnant, and nursing mothers. (17) Not appropriate for the study at the physician's assessment.
Target sample size	50

Research contact person
Name of lead principal investigator	Goro Nakayama
Organization	Nagoya University Graduate School of Medicine
Division name	Department of Gastroenterological Surgery
Address	65 Tsurumai-cho, Showa-ku, Nagoya-city, Aichi, Japan
TEL	052-744-2253
Email	goro@med.nagoya-u.ac.jp

Public contact
Name of contact person	Miyuki Aoki
Organization	Chubu Clinical Oncology Group (CCOG)
Division name	Data Center
Address	65 Tsurumai-cho, Showa-ku, Nagoya-city, Aichi, Japan
TEL	(81)52-744-2253
Homepage URL	http://www.med.nagoya-u.ac.jp/surgery2/scientific/ccog/
Email	goro@med.nagoya-u.ac.jp

Sponsor
Institute	Chubu Clinical Oncology Group (CCOG)
Institute
Department

Funding Source
Organization	None
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	2011 Year 10 Month 05 Day

Progress
Recruitment status	Main results already published
Date of protocol fixation	2010 Year 03 Month 15 Day
Anticipated trial start date	2010 Year 04 Month 01 Day
Last follow-up date	2015 Year 09 Month 15 Day
Date of closure to data entry	2015 Year 09 Month 30 Day
Date trial data considered complete	2015 Year 12 Month 31 Day
Date analysis concluded	2016 Year 05 Month 06 Day

Related information
URL releasing protocol
Publication of results	Partially published
URL releasing results
Results
Other related information

Management information
Registered date	2011 Year 10 Month 05 Day
Last modified on	2016 Year 11 Month 16 Day

Link to view the page
URL(English)	https://upload.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000007690