Effects of S-1 and Capecitabine on Coronary Artery Blood Flow

Colon Cancer Clinical Trial

— FluoHeart  

Official title:

Effects of S-1 and Capecitabine in Combination With Oxaliplatin on the Coronary Artery Blood Flow in Patients Metastatic Gastrointestinal Tract Adenocarcinoma: a Randomized Phase II Study

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02216149
• Other study ID #: HUS-01/2013
• Secondary ID: 2013-003976-11
• Status: Terminated
• Phase: Phase 2
• Start date: January 2015
• Est. completion date: August 2018

Study information

• Verified date: August 2018
• Source: Helsinki University Central Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Fluoropyrimidine chemotherapy agents , such as 5-fluorouracil and capecitabine, are occasionally associated with cardiac toxicity. Clinical fluoropyrimidine cardiotoxicity is infrequent, but subclinical toxicity may be much more common. Cardiac toxicity may be less frequent with S-1 as compared with 5-fluorouracil and capecitabine, but head-to-head comparisons are lacking. The purpose of the study is to compare 2 measures of subclinical coronary artery microvascular dysfunction, the coronary flow reserve and the coronary flow response to a cold pressor test, in a patient population who are being treated for adenocarcinoma of the gastrointestinal tract with one of 2 oxaliplatin-containing regimens, either with oxaliplatin plus S-1 or with oxaliplatin plus capecitabine.

Description:

Patients diagnosed with adenocarcinoma of the gastroesophageal tract are randomly assigned to receive two 3-weekly cycles of either XELOX (intravenous oxaliplatin 130 mg/m2 d.1 followed by oral capecitabine 2000 mg/m2/day divided in 2 daily doses d1-14) or SOX (intravenous oxaliplatin 130 mg/m2 d. 1 followed by oral S-1 25 mg/m2/day BID d1-14). A cross-over between the 2 arms is carried out after the first 2 cycles; patients allocated to XELOX will receive 2 cycles of SOX (cycles 3 and 4), and those allocated to SOX will receive XELOX (cycles 3 and 4). Monitoring of the coronary artery flow, cardiac arrythmias, cardiac symptoms and blood biochemistry is done at baseline, during each chemotherapy cycle (cycles 1 to 4) and after treatment.Study treatment will continue until all patients have discontinued from treatment or maximum 24 weeks from the date of the first day of treatment, whichever occurs first. At that point, treatment may continue at the discretion of the Investigator. Each patient will be followed for survival status for a minimum of 12 months after first dose of study medication. Tumor assessments will be performed throughout the study period and analyzed using Response Evaluation Criteria in Solid Tumors (RECIST) criteria (Version 1.1, 2009). Computed tomography (CT) scans will be performed at the end of every 2 cycles. Cardiac assessments will be performed and analyzed using non-invasive transthoracic Doppler echocardiography, 24-h Holter registration, and plasma troponin concentration.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 20
• Est. completion date: August 2018
• Est. primary completion date: August 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 100 Years

Eligibility

Inclusion Criteria:

• Has given written informed consent.

• Is at least 18 years of age.

• Has advanced or metastatic gastrointestinal tract adenocarcinoma.

• No previous cancer chemotherapy for cancer.

• Measurable or evaluable lesions according to RECIST v1.1 criteria.

• Is able to take medications orally.

• Has ECOG performance status 0 or 1.

• Has a life expectancy of at least 3 months.

• Has adequate organ function.

Exclusion Criteria:

• Cancer considered operable without prior chemotherapy.

• Prior chemotherapy to cancer.

• Previous therapy with fluoropyrimidines or anthracyclines for any indication.

• Inability to swallow tablets.

• Known brain metastasis or leptomeningeal metastasis.

• History of myocardial infarction, coronary stenting/graft.

• History of unstable angina, coronary/peripheral artery bypass graft.

• History of cerebrovascular accident or transient ischemic attack.

• History of pulmonary embolism or deep vein thrombosis.

• Symptomatic congestive heart failure.

• Ongoing cardiac dysrhythmias.

• Patients with any cardiac disease that requires regular medication.

• Hypertensive crisis or severe hypertension that is not controlled.

• Is a pregnant or lactating female.

• The cardiac arterial flow tests cannot be done.

Related Conditions & MeSH terms

• Colon Cancer
• Esophageal Neoplasms
• Esophagus Cancer
• Rectal Neoplasms
• Rectum Cancer
• Small Bowel Cancer
• Stomach Cancer
• Stomach Neoplasms

Intervention

Drug:
• S-1
S-1 25 mg/m2/day BID d1-14, oxaliplatin injection 130 mg/m2 D1 every 3 weeks
• Capecitabine
capecitabine 2000 mg/m2/day divided in 2 daily doses d1-14, oxaliplatin injection 130 mg/m2 D1 every 3 weeks
• Oxaliplatin
Oxaliplatin 130 mg/m2 D1 every 3 weeks

Locations

Country	Name	City	State
Finland	Helsinki University Central Hospital	Helsinki

Sponsors (1)

Lead Sponsor	Collaborator
Heikki Joensuu

Country where clinical trial is conducted

Finland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Frequency of coronary artery dysfunction	The frequency of subclinical coronary artery dysfunction is as assessed by comparing the coronary flow reserve during chemotherapy with the baseline coronary flow reserve, and the coronary flow response to a cold pressor test.	3 months
Secondary	Coronary artery blood flow rate	The coronary artery blood flow rate is measured with ultrasound. The rates are compared with the baseline and between the groups.	3 months
Secondary	Cardiac arrythmias during 24-hour electrocardiogram registration	Cardiac arrythmias detected with Holter cardiac recording.	3 months
Secondary	Adverse events between the allocation groups	by CTCAE.4	3 months
Secondary	Response to chemotherapy	by RECIST 1.1	3 months
Secondary	Survival status	Survival from the first dose of study medication to study completion	12 months