Safety Study of Capecitabine With Radiation in Elderly Rectal Cancer
Phase I Study of Preoperative Concurrent Chemo-radiation With Capecitabine in Elderly Rectal Cancer Patients
1 other identifier
interventional
24
1 country
1
Brief Summary
This phase I study is designed to determine the maximum tolerant dose of capecitabine when used in preoperative concurrent chemo-radiation for locally advanced rectal patients over 75 years old.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_1
Started Jan 2011
Typical duration for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2011
CompletedFirst Submitted
Initial submission to the registry
April 20, 2012
CompletedFirst Posted
Study publicly available on registry
April 25, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2014
CompletedResults Posted
Study results publicly available
April 20, 2015
CompletedApril 20, 2015
April 1, 2015
3.3 years
April 20, 2012
April 7, 2015
April 17, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of Participants Experienced Dose Limited Toxicity
Dose related toxicity is defined as follows:1. luecopenia \> grade 2; granular cell decrease \> grade 2; anemia \> grade 1; platelet \> grade 1;SGPT/SGOT elevation \> grade 1; ALP \> grade 1; GGT \> grade 1; Tbil \> grade 1;renal function damag \> grade 2;Non-gradular cell decreased fever \> grade 1;nausea/vomiting \> grade 1; fatigue \> grade 2; weight loss \> grade 2;gastritis \> grade 2; dairrea \> grade 2; abdominal pain \> grade 2; upper gastrointestinal bleeding \> grade 1;other toxic reaction \> grade 2;KPS \< 50 during the treatment
up to 7 weeks from start of the treatment
Study Arms (5)
1000mg
EXPERIMENTALcapecitabine 1000mg/m2/d d1-14, d22-25 combined with concurrent radiotherapy will be given to enrolled patients.
1200mg
EXPERIMENTALcapecitabine 1200mg/m2/d d1-14, d22-35 combined with concurrent radiotherapy will be given to enrolled patients.
1350mg
EXPERIMENTALcapecitabine 1300mg/m2/d d1-14, d22-35 combined with concurrent radiotherapy will be given to enrolled patients.
1500mg
EXPERIMENTALcapecitabine 1500mg/m2/d d1-14, d22-35 combined with concurrent radiotherapy will be given to enrolled patients.
1650mg
EXPERIMENTALcapecitabine 1650mg/m2/d d1-14, d22-35 combined with concurrent radiotherapy will be given to enrolled patients.
Interventions
oral pills, 1000mg/m2/d, split in two times, d1-14, d22-35 combined with concurrent pelvic radiation
Eligibility Criteria
You may qualify if:
- rectal adenocarcinoma, clinical stage II/III(T3-4 or N+, AJCC 7th).
- KPS status no less than 70; Charlson comorbidity no more than 3.
- life expectancy more than 6 months.
- hemoglobin \>= 100g/L, white blood cell \>= 3.5\*10E9/L, neutrophil \>= 1.5\*10E9/L, platelet \>= 100\*10E9/L.Creatin normal, Total bilirubin normal, AST and AST normal, AKP normal.
- do not have allergy history to thymidine phosphorylase.
- do not receive surgery ( except palliative colostomy) or chemotherapy or other anti-cancer treatment
- no previously pelvic irradiation history
- informed consent signed
You may not qualify if:
- other cancer history, except curable non-melanoma skin cancer or cervix in-situ carcinoma
- previous pelvic irradiation history
- receiving surgery (except palliative colostomy), chemotherapy or other anti-cancer treatment
- allergy history to thymidine phosphorylase
- active infection existed
- severe complication, such as acute myocardial infarction in 6 months, uncontrolled diabetes ( Plasma glucose concentrations in any time of a day≥11.1mmol/L), severe cardiac arrhythmia, etc.
- anticipate other clinical trials in four weeks before enrollment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
radiation department, Cancer Hospital, CAMS
Beijing, Beijing Municipality, 100021, China
Related Publications (54)
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MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Results Point of Contact
- Title
- Dr. Jing Jin
- Organization
- Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College
Study Officials
- PRINCIPAL INVESTIGATOR
Jing Jin, Ph.D.
Chinese Academic Medical Science
- PRINCIPAL INVESTIGATOR
Yexiong Li, Ph.D.
Chinese Academic Medical Science
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- vice chair of radiation department
Study Record Dates
First Submitted
April 20, 2012
First Posted
April 25, 2012
Study Start
January 1, 2011
Primary Completion
May 1, 2014
Study Completion
May 1, 2014
Last Updated
April 20, 2015
Results First Posted
April 20, 2015
Record last verified: 2015-04