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

Heikki Joensuu

Status and phase: Terminated; Phase 2

Conditions: Esophagus Cancer; Rectum Cancer; Colon Cancer; Stomach Cancer; Small Bowel Cancer

Treatments: Drug: S-1; Drug: Capecitabine; Drug: Oxaliplatin

Study type: Interventional

Funder types: Other

Identifiers

NCT02216149

2013-003976-11 (EudraCT Number)

HUS-01/2013

Details and patient eligibility

About

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.

Full 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.

Enrollment: 20 patients

Sex: All

Ages: 18 to 100 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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20 participants in 2 patient groups

S-1 plus oxaliplatin (SOX)

Experimental group

Description:

Oxaliplatin 130 mg/m2 d. 1 followed by oral S-1 25 mg/m2/day BID d1-14.

Treatment:

Drug: Oxaliplatin

Drug: S-1

Oxaliplatin plus capecitabine (XELOX)

Active Comparator group

Description:

Intravenous oxaliplatin 130 mg/m2 d.1 followed by oral capecitabine 2000 mg/m2/day divided in 2 daily doses d1-14.

Treatment:

Drug: Oxaliplatin

Drug: Capecitabine