Rectal CancerPhase 2NCT02288078
Oral Steroids for Regorafenib-induced Fatigue/Malaise in Unresectable mCRC (KSCC1402/HGCSG1402)
A Phase 2 study testing General condition, Blood pressure and Patient Reported Outcome in people with Rectal Cancer, run by Clinical Research Support Center Kyush at 1 site in Japan.
Trial summary
The objective of this randomized placebo-controlled Phase 2 study is to evaluate prophylactic effects of dexamethasone for fatigue and malaise (weakness, lethargy, malaise) resulting from regorafenib treatment, as well as to assess treatment continuation of regorafenib. Read more about this study
- Who is it for?
- Ages 20 years and older
- Conditions the study is for
- Rectal Cancer
- What is being tested?
- General condition, Blood pressure and Patient Reported Outcome
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 74 participants
- Where
- 1 siteJapan
- Study dates
- Oct 2014to Sep 2016
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Capable of granting informed consent in writing for receiving treatment outlined in this protocol
- The investigators determines that the patient can receive the treatment outlined in this protocol
- Histological diagnosis of adenocarcinoma of either the colon or the rectum, regardless of RAS mutation
- Metastatic colorectal cancer scheduled for treatment with regorafenib
- Lesions are either measurable or non-measurable according to RECIST ver. 1.1
- Contrasted torso CT within 28 days before enrollment
Show all 10Show fewer
- At least 20 years of age
- PS 0-1
- Bone marrow, hepatic, and renal functions have all been confirmed as normal within 14 days prior to initiation of regorafenib treatment
- Life expectancy of at least 3 months
Who cannot join
- Used regorafenib previously
- Blood transfusion or granulocyte-colony stimulating factor (G-CSF) administration within 14 days
- Grade 2 or higher fatigue or malaise or asthenia according to NCI-CTCAE ver. 4.0
- History of a different type of cancer according to histological findings or cancer of a different primary focus within the past 5 years. The following are excluded: carcinoma in situ of the cervix, non-melanoma skin cancer, superficial bladder cancer (Ta, Tis, and T1), gastric cancer,non-invasive breast cancer, etc
- Highly invasive surgery, an open biopsy, or who have received significant trauma within 28 days of initiating regorafenib treatment
- Congestive cardiac failure of New York Heart Association (NYHA) >=Class 2
Show all 34Show fewer
- Unstable angina (symptoms at rest),new-onset angina (onset within past 3 months), or a history of myocardial infarction within 6 months of initiating treatment
- Arrhythmia requiring treatment with anti-arrhythmia drugs
- Uncontrollable hypertension
- Pleural effusion or ascites causing dyspnea (NCI-CTCAE >=Grade 2)
- History of venous or arterial thrombosis or embolism within 6 months prior to initiation of treatment, including cerebrovascular accidents, deep vein thrombosis, or pulmonary embolism
- Patients with active infections of NCI-CTCAE >=Grade 3
- Positive for either hepatitis B (HB)s antigen or hepatitis C virus (HCV) antibody
- Seizure disorders requiring drug treatment
- Cerebral metastases or history of such
- History of organ transplant
- Symptoms or history of hemorrhagic tendency, regardless of severity
- Some form of hemorrhaging (NCI-CTCAE >=Grade 2) within 4 weeks prior to initiating treatment
- Incurable wound, fracture or ulcer
- Renal failure requiring either hemodialysis or peritoneal dialysis
- Dehydration symptoms of NCI-CTCAE >=Grade 1
- Abusing drugs or who are in a physical, psychological, or social state which might impair study participation or evaluation of results
- Interstitial lung disease with active signs or symptoms
- Have difficulty taking oral drugs
- Digestion absorption disorders
- Adverse events resulting from previous treatments or procedures which have not yet resolved (NCI-CTCAE >=Grade 2)
- Received systemic anti-cancer treatments within 2 weeks prior to initiation of regorafenib treatment, including chemotherapy, molecular target drugs, immunotherapy, or hormone therapy
- Poorly controlled glucose tolerance abnormalities due to diabetes mellitus (patients using insulin)
- Active GI ulcers or a history of such
- Glaucoma
- Oral steroids are otherwise contraindicated
- Either pregnant or nursing. Women who may become pregnant must have a negative pregnancy test within 7 days prior to initiating treatment
- Women who may become pregnant, or men whose partners may become pregnant, must agree to use appropriate contraceptives from granting of consent to 3 months after conclusion of regorafenib therapy
- Other illnesses or conditions which, according to the judgment of the investigator, may result in physical harm caused by the study, or which may impair study compliance
Trial locations and contacts
1 site in 1 country.
Yuji Miyamoto, MD, PhD contact
Yasunori Emi, MD, PhD contact
Japan1 site, 1 recruiting
- Recruiting
Saiseikai Fukuoka General Hospital
Fukuoka, 810-0001
Yasunori Emi, MD, PhD, +81-92-771-8151, emi-y@saiseikai-hp.chuo.fukuoka.jp
About this study
Official title: A Study of Prophylactic Oral Steroids for Fatigue and Malaise Due to Regorafenib Treatment for Unresectable Metastatic Colorectal Cancer: a Randomized, Placebo-controlled, Double-blind Phase 2 Clinical Study (KSCC1402/HGCSG1402)
The objective of this randomized placebo-controlled Phase 2 study is to evaluate prophylactic effects of dexamethasone for fatigue and malaise (weakness, lethargy, malaise) resulting from regorafenib treatment, as well as to assess treatment continuation of regorafenib.
Read the detailed description
- Patient registration procedure If it is confirmed that the subject meets the inclusion criteria and correspondent none of the exclusion criteria, the subject is registered by using Clinical Research Support Center (CReS) Kyushu registration/allocation system. The registration with the registration/allocation system is available for 24 hr (URL: https://reg.cres-kyushu.or.jp/qmin/login/) and needs for individual identifier (ID) and password.
- Quality management
- Preparation and management of the test drugs
The test drugs are an active drug, which is a capsule filled with dexamethasone powder and lactose, and a placebo, which is a capsule filled with only lactose. The test drugs will be prepared by the Department of Pharmacy (manager: Professor Masuda), Kyushu University Hospital in accordance with the procedures for preparation of the test drugs. Dexamethasone powder and lactose will be purchased by Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University from Tomita Pharmaceutical and delivered to the pharmacy department. Research funds will be used for the purchase. The capsule will be purchased from Tomita Pharmaceutical. The test drugs will be delivered to CReS-Kyushu (enrollment/data center) and managed using a double-blind method in accordance with the procedures. The double-blind code will be kept by the person responsible for management of the test drugs Shoji Tokunaga, Medical Information Center, Kyushu University, and a backup of the code will be kept by Hidekazu Aratani of CReS-Kyushu.
The test drugs will be managed according to the investigational drug number and stored at the warehouse of the Fukuoka branch of Yamato Logistics Co., Ltd. The warehouse is certified to store drugs for humans for more than 2 years under the supervision of pharmacists.
In the participating medical institution, manager and vice manager for the management of the test drugs will be appointed. It is preferable that the manager and vice managers are selected from among personnel who are experienced in drug management including personnel from the Department of Pharmacy or clinical trial management office. The manager is not allowed to become the investigator or sub-investigator. A physician who may treat subjects is not allowed to become the manager.
The electronic data capture (EDC) system will be used for communications between the enrollment/data center, Yamato Logistics and participating medical institution. Information on subjects will be reported by e-mail to the data center, and the data center will ensure the information by telephone to Yamato Logistics and the investigational drug management division of the medical institution. The test drugs will be delivered by Yamato Logistics to the medical institution. The test drugs for only a subject will be delivered once (allocation adjustment factor). Considering that a number of days are necessary for delivery, there should be at least 3 working days between enrollment and start of treatment. The interval between enrollment and start of treatments should be up to 14 days. Physicians treating subjects are not allowed to manage the test drugs. The vice manager will manage the test drugs according to subjects under the supervision of the manager. Orders for the test drugs will be made by letter or e-mail in accordance with the medical institution's procedures. A sufficient number of capsules of the test drugs until the next hospital visit will be ordered/prescribed once. If the test drugs are used properly in accordance with the protocol, an order/prescription for the test drugs will be made every 7 days. Subjects (patients) will be advised to keep records of the use of regorafenib and test drugs in the medication diary. The remaining number of capsules of the test drugs will be checked in consideration of the use of the test drugs. The remaining test drugs will be returned to the study office. In accordance with the protocol, the test drugs should be prescribed for 28-day treatment, but will be prescribed for 30-day treatment considering loss and damage. The test drug for 2-day treatment should be left unused when treatment is completed. The remaining test drugs will be returned to the enrollment/data center.
When the test drugs are delivered, the enrollment number, investigational drug number, reception date, the number of capsules of the test drugs delivered will be entered in the EDC system. Also, the number of capsules prescribed, date of prescription, remaining number of capsules (total number of capsules stored including the number of capsules returned), confirmation date of completion/discontinuation of the protocol treatment, total remaining number of capsules including the number of capsules returned will be entered in the EDC system.
The number of capsules lost and reasons for the loss will be entered in the EDC system.
- Monitoring
A central monitoring or in-site monitoring are carried out based on the data from case report form (CRF) collecting at data coordinating center. In principle, an on-site monitoring is not carried out, but it may be carried out when the on-site monitoring is determined to need by Kyushu Study group of Clinical Cancer (KSCC) steering committee from the results of the central monitoring so on.
Data Monitoring Committee A Data Monitoring Committee (DMC) has been established.
- Data entry all data will be entered by the double entry method. Referential data rules, valid values, range checks, and consistency checks against data already stored in the database will be supported. Checks will be applied at the time of data entry into a specific field. Additional errors will be detected by programs designed to detect missing data or specific errors in the data. The investigator who receives the inquiry will respond by checking the original forms for inconsistency, checking other sources to determine the correction, modifying the original paper form entering a response to the query.
- Regular monitoring report
A regular monitoring report generated by data coordinating center is submitted to KSCC Steering Committee, principal investigator, the DMC etc and it is reviewed according to "KSCC regulation on the monitoring". The information on the status of site ethics committee (EC) approval and the achievement of enrollment: number of enrollment- total/per periodical, total/per site, is reported monthly using e-mail.
- Contents of monitoring report
Study abstract: schema/purpose/subject/endpoint/definition of treatment/anticipated enrollment number/progress of the study Enrollment status: per participating site/total Monitoring activity: contents of activity/CRF collection per site/uncollected CRF, inquiry Review of the eligible treatment case：the case of ineligible possibility/the case determined as ineligible/number of eligible case/the case determined as non-treatment/total number of treatment case Review of a target population for analysis: the number of cases targeted for efficacy analysis/safety analysis Patient background Treatment time-course: summary of on-treatment and discontinuation/summary of reason for discontinuation/list of reason for discontinuation Protocol violation/deviation Safety evaluation: serious adverse reaction, event/the case which was notified to the study group among the adverse reactions, events with an ordinary report/general adverse events Others
- Audit
A site audit is carried out by the audit members of KSCC Coordinating Center, data coordinating center, medical staff of other site under the approval of the site director according to "KSCC regulation for site audit". The results of the audit are reported to the site director, KSCC Steering Committee, principal investigator etc. (if required, to DMC).
- Conditions
- Rectal Cancer
- Being tested
- General condition, Blood pressure, Patient Reported Outcome, Clinical findings, Hematology/blood chemistry
- Keywords
- unresectable colorectal cancer, regorafenib, Steroid, fatigue and malaise, Phase 2 randomized, controlled trial (RCT)
- Medical subject headings
- Rectal Neoplasms, Fatigue
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
General conditionOther
Eastern Cooperative Oncology Group (ECOG) performance status (PS), height and body weight
Blood pressureOther
systolic blood pressure (SBP)/diastolic blood pressure (DBP)
Patient Reported OutcomeOther
Also called PRO
Incidence of fatigue or malaise (All grade of CTCAE ver. 4), anorexia, Brief fatigue inventory (BFI), FACT-C.
Clinical findingsOther
- Blood and lymphatic system disorders: febrile neutropenia
- Gastrointestinal disorders: constipation, diarrhea, oral mucositis, nausea, and vomiting
- General disorders and administration site conditions: fatigue and malaise
- Immune system disorders: allergic reaction
- Metabolism and nutrition disorders: anorexia
- Nervous system disorders: dysgeusia and peripheral sensory neuropathy
- Respiratory, thoracic and mediastinal disorders: hoarseness (change of voice)
- Skin and subcutaneous tissue disorders: alopecia, skin hyperpigmentation, urticaria, and palmar-plantar erythrodysesthesia syndrome
- Vascular disorders: hypertension
- Symptomatic pancreatitis
Hematology/blood chemistryOther
White blood cell count, absolute neutrophil count (stab + segmented), hemoglobin, platelet count, albumin, total bilirubin, aspartate aminotransferase(AST) (GOT), alanine aminotransferase (ALT) (GPT), serum creatinine, Na, K
Coagulation and fibrinolysis systemOther
international normalized ratio (INR)
UrinalysisOther
Proteinuria (qualitative)
Medication checkOther
Medicine taking situation (regorafenib, dexamethasone and placebo) determined by subject's diary at every courses
Adverse eventOther
Also called AE
CTCAE ver.4.0
Thyroid function testOther
Thyroid-stimulating hormone (TSH), T4, and T3
Contrast-enhanced torso CTOther
It is recommended that CT images should be taken every 4 weeks (if possible) or at least every 8 weeks (allowable time window: ± 2 weeks), with the treatment phase taken into consideration.
Brain MRIOther
If any symptom of brain metastasis is suspected
DexamethasoneDrug
Also called DX
Capsule filled with dexamethasone and lactose
RegorafenibDrug
Also called Stivarga
Film-coating tablet contains 40 mg of regorafenib
PlaceboDrug
Also called PL
Capsule filled with lactose
Proton pump inhibitorDrug
Also called PPI
PPIs (omeprazole, lansoprazole, etc, as not specified) for prevention of peptic ulcer
| Study group | Role | What they receive |
|---|---|---|
| Treatment group | Active comparator | Treatment with regorafenib (160 mg/day, oral administration, 3 weeks on therapy followed by 1 week off therapy), test drug capsule (dexamethasone 2 mg) and proton pump inhibitors (PPIs) will be started within 14 days of enrollment. The protocol treatment period is 4 weeks.
Follow-up treatment for the underlying disease after the 4-week protocol treatment is not specified. The physician in charge will decide whether or not to continue treatment with regorafenib. For the prevention of fatigue/malaise, dexamethasone 2 mg can be used.
General condition, blood pressure, Patient Reported Outcome, clinical findings, hematology/blood chemistry, coagulation and fibrinolysis system, urinalysis, medicatiob check, adverse event, thyroid function test, brain MRI, Contrast-enhanced torso CT Receives: Other: General condition; Other: Blood pressure; Other: Patient Reported Outcome; Other: Clinical findings; Other: Hematology/blood chemistry; Other: Coagulation and fibrinolysis system; Other: Urinalysis; Other: Medication check; Other: Adverse event; Other: Thyroid function test; Other: Contrast-enhanced torso CT; Other: Brain MRI; Drug: Dexamethasone; Drug: Regorafenib; Drug: Proton pump inhibitor |
| Placebo group | Placebo comparator | Treatment with regorafenib (160 mg/day, oral administration, 3 weeks on therapy followed by 1 week off therapy), placebo capsule (lactose) and proton pump inhibitors (PPIs) will be started within 14 days of enrollment. The protocol treatment period is 4 weeks.
Follow-up treatment for the underlying disease after the 4-week protocol treatment is not specified. The physician in charge will decide whether or not to continue treatment with regorafenib. For the prevention of fatigue/malaise, dexamethasone 2 mg can be used.
General condition, blood pressure, Patient Reported Outcome, clinical findings, hematology/blood chemistry, coagulation and fibrinolysis system, urinalysis, medication check, adverse event, thyroid function test, brain MRI, Contrast-enhanced torso CT Receives: Other: General condition; Other: Blood pressure; Other: Patient Reported Outcome; Other: Clinical findings; Other: Hematology/blood chemistry; Other: Coagulation and fibrinolysis system; Other: Urinalysis; Other: Medication check; Other: Adverse event; Other: Thyroid function test; Other: Contrast-enhanced torso CT; Other: Brain MRI; Drug: Regorafenib; Drug: Placebo; Drug: Proton pump inhibitor |
What is being measured
The primary outcome is the main question the study is designed to answer.
incidence of fatigue or malaise (CTCAE ver. 4, all grades)
With the number of subjects in safety analysis set (SAS) as the denominator, the frequency of the worst grade of "fatigue" or "malaise"(according to CTCAE ver.4.0) is determined.
Measured: 4weeks
Secondary outcomes (3)
brief fatigue inventory （Patient Reported Outcome）
For all subjects enrolled in the present clinical study, the severity of fatigue/malaise is rated using the brief fatigue inventory (BFI) scale obtained every week following the start. Mean of numerical evaluating scale from 9 questions is defined as the global fatigue score. Details of the method to collect and analyze the BFI as a patient reported outcome (PRO) will be specified in a procedure separately prepared along the instruction by Professor Yamaguchi (Tohoku University).
Measured: 4weeks
adverse events
With the number of subjects in whom at least a part of the protocol treatment is provided (all treated subjects) set as the denominator, the frequencies of the following adverse events/toxicity (according to CTCAE ver.4.0) appearing at the worst grade whenever during the entire treatment course are determined by treatment group. Whether ineligible subjects are included in the analysis set or not is decided by the KSCC's research administration office through discussion with the Registration/Data Center.
With the number of subjects in Full analysis set (FAS) set as the denominator, the rate of treatment discontinuation due to adverse events other than disease progression is determined.
Measured: 1year
relative dose intensity (regorafenib)
With the planned dose of regorafenib in 1 course set as the denominator while the actual dose set as the numerator, the relative dose intensity (given in percentage) is determined for the FAS.
Measured: 4weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Nov 2014 (estimated)
- Study startOct 2014
- Primary completionSep 2015 (estimated)
- Study completionSep 2016 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Rectal CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 74 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Clinical Research Support Center Kyush
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Hideo Baba, Kumamoto University
- Investigators
- Yasunori Emi, MD, PhD, Study director, Saiseikai Fukuoka General Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02288078
- Sponsor's protocol ID
- KSCC1402/HGCSG1402
- Other IDs
- UMIN000015131
- Status last verified
- Nov 2014
- First submitted
- 28 Oct 2014
- Last updated
- 13 Nov 2014
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 13 Nov 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Study of Prophylactic Oral Steroids for Fatigue and Malaise Due to Regorafenib Treatment for Unresectable Metastatic Colorectal Cancer: a Randomized, Placebo-controlled, Double-blind Phase 2 Clinical Study (KSCC1402/HGCSG1402)
- ClinicalTrials.gov ID
- NCT02288078
- Acronym / sponsor ID
- KSCC1402/HGCSG1402
- Conditions
- Rectal Cancer
- Keywords
- unresectable colorectal cancer, regorafenib, Steroid, fatigue and malaise, Phase 2 randomized, controlled trial (RCT)
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 74 participants (estimated)
- Lead sponsor
- Clinical Research Support Center KyushUniversity, hospital or other
- Study start
- Oct 2014
- Primary completion
- Sep 2015 (estimated)
- Study completion
- Sep 2016 (estimated)
- First posted
- 11 Nov 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The objective of this randomized placebo-controlled Phase 2 study is to evaluate prophylactic effects of dexamethasone for fatigue and malaise (weakness, lethargy, malaise) resulting from regorafenib treatment, as well as to assess treatment continuation of regorafenib.
Detailed description
- Patient registration procedure If it is confirmed that the subject meets the inclusion criteria and correspondent none of the exclusion criteria, the subject is registered by using Clinical Research Support Center (CReS) Kyushu registration/allocation system. The registration with the registration/allocation system is available for 24 hr (URL: https://reg.cres-kyushu.or.jp/qmin/login/) and needs for individual identifier (ID) and password.
- Quality management
- Preparation and management of the test drugs
The test drugs are an active drug, which is a capsule filled with dexamethasone powder and lactose, and a placebo, which is a capsule filled with only lactose. The test drugs will be prepared by the Department of Pharmacy (manager: Professor Masuda), Kyushu University Hospital in accordance with the procedures for preparation of the test drugs. Dexamethasone powder and lactose will be purchased by Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University from Tomita Pharmaceutical and delivered to the pharmacy department. Research funds will be used for the purchase. The capsule will be purchased from Tomita Pharmaceutical. The test drugs will be delivered to CReS-Kyushu (enrollment/data center) and managed using a double-blind method in accordance with the procedures. The double-blind code will be kept by the person responsible for management of the test drugs Shoji Tokunaga, Medical Information Center, Kyushu University, and a backup of the code will be kept by Hidekazu Aratani of CReS-Kyushu.
The test drugs will be managed according to the investigational drug number and stored at the warehouse of the Fukuoka branch of Yamato Logistics Co., Ltd. The warehouse is certified to store drugs for humans for more than 2 years under the supervision of pharmacists.
In the participating medical institution, manager and vice manager for the management of the test drugs will be appointed. It is preferable that the manager and vice managers are selected from among personnel who are experienced in drug management including personnel from the Department of Pharmacy or clinical trial management office. The manager is not allowed to become the investigator or sub-investigator. A physician who may treat subjects is not allowed to become the manager.
The electronic data capture (EDC) system will be used for communications between the enrollment/data center, Yamato Logistics and participating medical institution. Information on subjects will be reported by e-mail to the data center, and the data center will ensure the information by telephone to Yamato Logistics and the investigational drug management division of the medical institution. The test drugs will be delivered by Yamato Logistics to the medical institution. The test drugs for only a subject will be delivered once (allocation adjustment factor). Considering that a number of days are necessary for delivery, there should be at least 3 working days between enrollment and start of treatment. The interval between enrollment and start of treatments should be up to 14 days. Physicians treating subjects are not allowed to manage the test drugs. The vice manager will manage the test drugs according to subjects under the supervision of the manager. Orders for the test drugs will be made by letter or e-mail in accordance with the medical institution's procedures. A sufficient number of capsules of the test drugs until the next hospital visit will be ordered/prescribed once. If the test drugs are used properly in accordance with the protocol, an order/prescription for the test drugs will be made every 7 days. Subjects (patients) will be advised to keep records of the use of regorafenib and test drugs in the medication diary. The remaining number of capsules of the test drugs will be checked in consideration of the use of the test drugs. The remaining test drugs will be returned to the study office. In accordance with the protocol, the test drugs should be prescribed for 28-day treatment, but will be prescribed for 30-day treatment considering loss and damage. The test drug for 2-day treatment should be left unused when treatment is completed. The remaining test drugs will be returned to the enrollment/data center.
When the test drugs are delivered, the enrollment number, investigational drug number, reception date, the number of capsules of the test drugs delivered will be entered in the EDC system. Also, the number of capsules prescribed, date of prescription, remaining number of capsules (total number of capsules stored including the number of capsules returned), confirmation date of completion/discontinuation of the protocol treatment, total remaining number of capsules including the number of capsules returned will be entered in the EDC system.
The number of capsules lost and reasons for the loss will be entered in the EDC system.
- Monitoring
A central monitoring or in-site monitoring are carried out based on the data from case report form (CRF) collecting at data coordinating center. In principle, an on-site monitoring is not carried out, but it may be carried out when the on-site monitoring is determined to need by Kyushu Study group of Clinical Cancer (KSCC) steering committee from the results of the central monitoring so on.
Data Monitoring Committee A Data Monitoring Committee (DMC) has been established.
- Data entry all data will be entered by the double entry method. Referential data rules, valid values, range checks, and consistency checks against data already stored in the database will be supported. Checks will be applied at the time of data entry into a specific field. Additional errors will be detected by programs designed to detect missing data or specific errors in the data. The investigator who receives the inquiry will respond by checking the original forms for inconsistency, checking other sources to determine the correction, modifying the original paper form entering a response to the query.
- Regular monitoring report
A regular monitoring report generated by data coordinating center is submitted to KSCC Steering Committee, principal investigator, the DMC etc and it is reviewed according to "KSCC regulation on the monitoring". The information on the status of site ethics committee (EC) approval and the achievement of enrollment: number of enrollment- total/per periodical, total/per site, is reported monthly using e-mail.
- Contents of monitoring report
Study abstract: schema/purpose/subject/endpoint/definition of treatment/anticipated enrollment number/progress of the study Enrollment status: per participating site/total Monitoring activity: contents of activity/CRF collection per site/uncollected CRF, inquiry Review of the eligible treatment case：the case of ineligible possibility/the case determined as ineligible/number of eligible case/the case determined as non-treatment/total number of treatment case Review of a target population for analysis: the number of cases targeted for efficacy analysis/safety analysis Patient background Treatment time-course: summary of on-treatment and discontinuation/summary of reason for discontinuation/list of reason for discontinuation Protocol violation/deviation Safety evaluation: serious adverse reaction, event/the case which was notified to the study group among the adverse reactions, events with an ordinary report/general adverse events Others
- Audit
A site audit is carried out by the audit members of KSCC Coordinating Center, data coordinating center, medical staff of other site under the approval of the site director according to "KSCC regulation for site audit". The results of the audit are reported to the site director, KSCC Steering Committee, principal investigator etc. (if required, to DMC).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Treatment group | Active comparator | Other: General condition, Other: Blood pressure, Other: Patient Reported Outcome, Other: Clinical findings, Other: Hematology/blood chemistry, Other: Coagulation and fibrinolysis system, Other: Urinalysis, Other: Medication check, Other: Adverse event, Other: Thyroid function test, Other: Contrast-enhanced torso CT, Other: Brain MRI, Drug: Dexamethasone, Drug: Regorafenib, Drug: Proton pump inhibitorTreatment with regorafenib (160 mg/day, oral administration, 3 weeks on therapy followed by 1 week off therapy), test drug capsule (dexamethasone 2 mg) and proton pump inhibitors (PPIs) will be started within 14 days of enrollment. The protocol treatment period is 4 weeks. Follow-up treatment for the underlying disease after the 4-week protocol treatment is not specified. The physician in charge will decide whether or not to continue treatment with regorafenib. For the prevention of fatigue/malaise, dexamethasone 2 mg can be used. General condition, blood pressure, Patient Reported Outcome, clinical findings, hematology/blood chemistry, coagulation and fibrinolysis system, urinalysis, medicatiob check, adverse event, thyroid function test, brain MRI, Contrast-enhanced torso CT |
| Placebo group | Placebo comparator | Other: General condition, Other: Blood pressure, Other: Patient Reported Outcome, Other: Clinical findings, Other: Hematology/blood chemistry, Other: Coagulation and fibrinolysis system, Other: Urinalysis, Other: Medication check, Other: Adverse event, Other: Thyroid function test, Other: Contrast-enhanced torso CT, Other: Brain MRI, Drug: Regorafenib, Drug: Placebo, Drug: Proton pump inhibitorTreatment with regorafenib (160 mg/day, oral administration, 3 weeks on therapy followed by 1 week off therapy), placebo capsule (lactose) and proton pump inhibitors (PPIs) will be started within 14 days of enrollment. The protocol treatment period is 4 weeks. Follow-up treatment for the underlying disease after the 4-week protocol treatment is not specified. The physician in charge will decide whether or not to continue treatment with regorafenib. For the prevention of fatigue/malaise, dexamethasone 2 mg can be used. General condition, blood pressure, Patient Reported Outcome, clinical findings, hematology/blood chemistry, coagulation and fibrinolysis system, urinalysis, medication check, adverse event, thyroid function test, brain MRI, Contrast-enhanced torso CT |
Who may qualify
- Ages
- 20 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (10 listed)
- Capable of granting informed consent in writing for receiving treatment outlined in this protocol
- The investigators determines that the patient can receive the treatment outlined in this protocol
- Histological diagnosis of adenocarcinoma of either the colon or the rectum, regardless of RAS mutation
- Metastatic colorectal cancer scheduled for treatment with regorafenib
- Lesions are either measurable or non-measurable according to RECIST ver. 1.1
Key exclusion criteria (34 listed)
- Used regorafenib previously
- Blood transfusion or granulocyte-colony stimulating factor (G-CSF) administration within 14 days
- Grade 2 or higher fatigue or malaise or asthenia according to NCI-CTCAE ver. 4.0
- History of a different type of cancer according to histological findings or cancer of a different primary focus within the past 5 years. The following are excluded: carcinoma in situ of the cervix, non-melanoma skin cancer, superficial bladder cancer (Ta, Tis, and T1), gastric cancer,non-invasive breast cancer, etc
- Highly invasive surgery, an open biopsy, or who have received significant trauma within 28 days of initiating regorafenib treatment
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| General conditionEastern Cooperative Oncology Group (ECOG) performance status (PS), height and body weight | Other | Placebo group, Treatment group |
| Blood pressuresystolic blood pressure (SBP)/diastolic blood pressure (DBP) | Other | Placebo group, Treatment group |
| Patient Reported OutcomeAlso: PROIncidence of fatigue or malaise (All grade of CTCAE ver. 4), anorexia, Brief fatigue inventory (BFI), FACT-C. | Other | Placebo group, Treatment group |
| Clinical findings* Blood and lymphatic system disorders: febrile neutropenia * Gastrointestinal disorders: constipation, diarrhea, oral mucositis, nausea, and vomiting * General disorders and administration site conditions: fatigue and malaise * Immune system disorders: allergic reaction * Metabolism and nutrition disorders: anorexia * Nervous system disorders: dysgeusia and peripheral sensory neuropathy * Respiratory, thoracic and mediastinal disorders: hoarseness (change of voice) * Skin and subcutaneous tissue disorders: alopecia, skin hyperpigmentation, urticaria, and palmar-plantar erythrodysesthesia syndrome * Vascular disorders: hypertension * Symptomatic pancreatitis | Other | Placebo group, Treatment group |
| Hematology/blood chemistryWhite blood cell count, absolute neutrophil count (stab + segmented), hemoglobin, platelet count, albumin, total bilirubin, aspartate aminotransferase(AST) (GOT), alanine aminotransferase (ALT) (GPT), serum creatinine, Na, K | Other | Placebo group, Treatment group |
| Coagulation and fibrinolysis systeminternational normalized ratio (INR) | Other | Placebo group, Treatment group |
| UrinalysisProteinuria (qualitative) | Other | Placebo group, Treatment group |
| Medication checkMedicine taking situation (regorafenib, dexamethasone and placebo) determined by subject's diary at every courses | Other | Placebo group, Treatment group |
| Adverse eventAlso: AECTCAE ver.4.0 | Other | Placebo group, Treatment group |
| Thyroid function testThyroid-stimulating hormone (TSH), T4, and T3 | Other | Placebo group, Treatment group |
| Contrast-enhanced torso CTIt is recommended that CT images should be taken every 4 weeks (if possible) or at least every 8 weeks (allowable time window: ± 2 weeks), with the treatment phase taken into consideration. | Other | Placebo group, Treatment group |
| Brain MRIIf any symptom of brain metastasis is suspected | Other | Placebo group, Treatment group |
| DexamethasoneAlso: DXCapsule filled with dexamethasone and lactose | Drug | Treatment group |
| RegorafenibAlso: StivargaFilm-coating tablet contains 40 mg of regorafenib | Drug | Placebo group, Treatment group |
| PlaceboAlso: PLCapsule filled with lactose | Drug | Placebo group |
| Proton pump inhibitorAlso: PPIPPIs (omeprazole, lansoprazole, etc, as not specified) for prevention of peptic ulcer | Drug | Placebo group, Treatment group |
Primary outcome
incidence of fatigue or malaise (CTCAE ver. 4, all grades)
Time frame: 4weeks
With the number of subjects in safety analysis set (SAS) as the denominator, the frequency of the worst grade of "fatigue" or "malaise"(according to CTCAE ver.4.0) is determined.
3 secondary outcomes
brief fatigue inventory （Patient Reported Outcome）
Time frame: 4weeks
adverse events
Time frame: 1year
relative dose intensity (regorafenib)
Time frame: 4weeks
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Nov 2014.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Yuji Miyamoto, MD, PhD contact
Yasunori Emi, MD, PhD contact
Yasunori Emi, MD, PhD study director
Saiseikai Fukuoka General Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing General condition, Blood pressure and Patient Reported Outcome in people with Rectal Cancer, run by Clinical Research Support Center Kyush at 1 site in Japan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 10 inclusion and 34 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 13 Nov 2014. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Japan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Yuji Miyamoto, MD, PhD (miyamotoyuji@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
incidence of fatigue or malaise (CTCAE ver. 4, all grades) (time frame: 4weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Nov 2014.