Sorafenib Plus Capecitabine Efficacy Assessment in Patients With Advanced Pre-treated Colorectal Cancer
18 Years
N/A
Both
Colorectal Cancer
Trial Information
Sorafenib Plus Capecitabine Efficacy Assessment in Patients With Advanced Pre-treated Colorectal Cancer
Treatment doses :
Sorafenib 200mg in the morning,400mg in the evening; escalation to 400mg twice daily after 1
cycle Capecitabine 850mg/m2 twice daily Oral Days 1-14, weeks 1-2
Fluoro-Deoxy Glucose Positron Emitting Tomography (FDG-PET)imaging at baseline and after
17-21 days while on therapy.
Sample size justification/statistical analysis
Sample size has been estimated in order to be able to test the null hypothesis that the
overall survival rate at 6 months is less than 30%. This hypothesis will be tested using a
binomial distribution. The study should be able to reject the null hypothesis, using a
1-sided test with α = 0.025, with a power of 90% in case of a true overall survival ≥ 50%
(rate at 6 months). The sample size required is 66 eligible patients (to be followed for 6
months minimum). Analysis will be done on all registered patients using an ITT approach on
all eligible patients.
A co-primary endpoint is to compare the overall survival of patients assessed as early PET
responders and of patients assessed as early PET non responders (the clinicians will remain
blinded for PET response assessment). For this primary analysis, patients who will undergo
the second PET assessment will be eligible and time zero for measuring survival will be the
date of this second PET examination. It is anticipated that 95% of the patients will be
eligible for the analysis with a 50% expected rate of early PET non-responders (result
obtained from an unpublished study conducted at Jules-Bordet Institute). With 66 patients
registered, we anticipate then that 63 patients will be available for the co-primary
endpoint. With 63 patients and our assumption that the HR for the comparison between the
survival distributions will be around 0.385 (based on the previously mentioned unpublished
study), we will need using a two-sided logrank test at the 2.5% level (2.5% chosen because
of the existence of 2 co-primary endpoints), 54 events (power of 90%). With 63 patients and
a follow-up after accrual of 1 year, we should reach this number of 54 events. However, to
account for another possible 5% drop-out (patient's refusal for undergoing the second PET
examination for instance), sample size should be increased to 70 eligible patients.
However, our estimation of 50% expected rate of early PET responders is coming from a
prospective unicentric cohort of 38 patients undergoing chemotherapy for 1st line or 2nd
line treatment of advanced colorectal cancer with a few of them having received biological
agents together with chemotherapy. Our estimation may then not be reliable due to small
sample size and different patients population. If this rate of early PET responders proves
to be higher, we should be prepared to increase our sample size for targeting the same power
of 90%. For instance, if the rate is 67% instead of 50%, the required number of events would
be 62 in-stead of 54. If the rate is 75%, the number of events should be increased to 73.
The number of patients would have then to be adapted according to the rate of evaluable
patients for this PET objective and the rate of patients lost to follow-up. For reassessing
the required numbers of events, we did not change our hypothesis of detecting, if true, a
hazard ratio of 0.385 in favor of early PET responders.
We plan, during the course of accrual, to assess the rate of patients evaluable for the PET
objective, of early PET responders and, if possible the rate of patients lost to follow-up
in order to check whether we need to review our planned sample size. However, no interim
analysis will be done on the primary endpoints.
Secondary endpoints are to estimate progression-free survival and objective response rate,
and to describe the adverse reactions associated with the study regimen in the study
population. Also, to determine the correlation of early metabolic response, as assessed by
FDG-PET/CT immediately before the first and the second cycles of treatment with the study
regimen, with overall survival, progression-free survival, and response rate, and to
determine the correlation of growth modulation index (GMI), defined as the time to
progression under the study regimen over the time to progression under the latest regimen
administered to the patient, with overall survival and progression-free survival.
The study is designed as a single-arm phase II study, with all patients accrued in one
stage. No early stopping rules will be used.
Inclusion Criteria:
- Participants must have histologically confirmed colorectal cancer that is metastatic
or unresectable and for which standard curative or palliative measures do not exist
or are no longer effective.
- All standard chemotherapy agents (fluoropyrimidines, irinotecan, and oxaliplatin) and
monoclonal antibodies (bevacizumab, cetuximab, and panitumumab) are allowed as
administered therapy before study entry. No more than two lines of treatment for
metastatic or recurrent disease are allowed, except for patients with KRAS-wt tumors,
for which third line with anti-EGFR agents is allowed.
- Age over 18 years.
- Life expectancy of greater than 12 weeks.
- ECOG performance status ≤ 1.
- Participants must have normal organ and marrow function as defined below:
- Leukocytes > 3,000/mcL
- Absolute neutrophil count > 1,500/mcL
- Platelets > 100,000/mcL
- total bilirubin within 2 × normal institutional limits
- AST/ALT/PAKL levels < 5 × institutional upper limit of normal
- creatinine within 2 × normal institutional limits or creatinine clearance > 35mL/min
- Women of child-bearing potential and men must agree to use adequate contraception
(hormonal or barrier method of birth control, abstinence) prior to study entry and
for the duration of study participation. Should a woman become pregnant or suspect
she is pregnant while participating in this study, she should inform her treating
physician immediately.
- Ability to understand and the willingness to sign a written informed consent
document.
Exclusion Criteria:
Participants who exhibit any of the following conditions at screening will not be eligible
for admission into the study.
- Participants who have had chemotherapy or radiotherapy within 4 weeks prior to
entering the study or those who have not recovered from adverse events due to agents
administered more than 4 weeks earlier.
- Participants may not be receiving any other experimental agents.
- Participants with known brain metastases should be excluded from this clinical trial
because of their poor prognosis and because they often develop progressive neurologic
dysfunction that would confound the evaluation of neurologic and other adverse
events.
- History of allergic reactions attributed to compounds of similar chemical or biologic
composition to sorafenib or capecitabine.
- Bleeding diathesis, history of cardiovascular ischemic disease or cerebrovascular
incident within the last six months, or major surgery within four weeks.
- Uncontrolled concurrent illness including, but not limited to ongoing or active
infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia, or psychiatric illness/social situations that would limit compliance with
study requirements.
- Pregnant women are excluded from this study because sorafenib and capecitabine are
antitumor agents with the potential for teratogenic or abortifacient effects. Because
there is an unknown but potential risk of adverse events in nursing infants secondary
to treatment of the mother with sorafenib or capecitabine, breastfeeding should be
discontinued if the mother is treated with sorafenib or capecitabine. These potential
risks may also apply to other agents used in this study.
- Uncontrolled Diabetes
- FDG PET/CT negative lesions or non metabolically assessable lesions (to small <2cm)
at the base line FDG PET/CT
- Individuals with a history of a different malignancy are ineligible except for the
following circumstances. Individuals with a history of other malignancies are
eligible if they have been disease-free for at least 5 years and are deemed by the
investigator to be at low risk for recurrence of that malignancy. Individuals with
the following cancers are eligible if diagnosed and treated within the past 5 years:
cervical cancer in situ, and basal cell or squamous cell carcinoma of the skin.
Type of Study:
Interventional
Study Design:
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Outcome Measure:
Overall survival at 6 months fixed endpoint
Outcome Description:
The 2 primary co-endpoints are : To obtain a preliminary assessment about the activity of the combination by estimating overall survival of the study population at a fixed time point (6 months) To compare as an exploratory analysis the overall survival of metabolic responders versus non-responders.
Outcome Time Frame:
6 months
Safety Issue:
Yes
Principal Investigator
Alain Hendlisz, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Institut Jules Bordet
Authority:
Belgium: Federal Agency for Medicinal Products and Health Products
Study ID:
EudraCT 2010-023695-91
NCT ID:
NCT01290926
Start Date:
February 2011
Completion Date:
July 2013
Related Keywords:
- Colorectal Cancer
- advanced chemorefractory colorectal cancer
- sorafenib
- capecitabine
- FDG-PET
- early metabolic response
- Colorectal Neoplasms
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