Study to Compare Cardiovascular Side Effects of Teysuno Versus Capecitabine

Pancreatic Cancer Clinical Trial

— TOFFEE  

Official title:

Toxicity OF Fluoropyrimidines: A Comparative Study of the Cardiotoxicity of capEcitabine and tEysuno

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01845337
• Other study ID #: 2012-005282-12
• Status: Completed
• Phase: Phase 2
• Start date: February 5, 2014
• Est. completion date: October 8, 2020

Study information

• Verified date: May 2023
• Source: University of Edinburgh
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Capecitabine is a chemotherapy drug used to treat many types of cancer including bowel and stomach cancer. Unfortunately a side effect of this drug is that it causes heart problems including heart attacks. An alternative drug, called teysuno is used extensively in other countries instead of capecitabine and appears to have less of a bad effect on the heart whilst still killing cancer cells. This study will investigate the effect of these two drugs on the heart and blood vessels and will be the first of its kind in humans.

Description:

Fluoropyrimidines (FPs) are widely used chemotherapy agents for the management of patients with colorectal, breast, upper gastrointestinal, head and neck cancers. Capecitabine is an oral prodrug of 5-fluorouracil (5FU) which is used extensively in the UK but is associated with clinically overt cardiotoxicity in up to 9% of patients. Cardiotoxicity occurs more commonly in patients with cardiovascular disease and manifests as chest pain, myocardial infarction, congestive heart failure, or sudden death with a mortality as high as 30%. In a study of continuous ECG Holter monitoring in patients receiving 5FU infusion, the majority (68%) of patients had ischaemic ECG changes and 2 patients died suddenly. We conducted a national survey of UK oncologists and 60% felt that 5FU/capecitabine cardiotoxicity was a significant problem in their clinical practice. Hypotheses for this toxicity include ischaemia secondary to coronary artery spasm, direct endothelial cell toxicity, myocardial toxicity and interactions with the coagulation system. Studies implicate a catabolite of 5FU, in particular fluoro-alanine (FBAL). FBAL is further metabolized to fluoroacetate (FAC), a cardiac toxin that inhibits mitochondrial aconitase, resulting in cell death. Teysuno is an oral fluoropyrimidine that has recently obtained a European licence. It is a combination of tegafur (5-FU prodrug), gimeracil (dihydropyrimidine dehydrogenase (DPD) inhibitor) and oteracil (phosphorylation inhibitor). There have been no reports of cardiac toxicity with teysuno. The incorporation of a DPD inhibitor should reduce FBAL concentrations which may prevent FP cardiotoxicity. However, this remains to be established.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 59
• Est. completion date: October 8, 2020
• Est. primary completion date: March 18, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 100 Years

Eligibility

Inclusion Criteria:

• Male or female patients at least 18 years or over with no upper age limit.
• Confirmed advanced or metastatic oesophageal, gastric, gastro-oesophageal, small bowel, colorectal, hepatobiliary or pancreatic cancer or cancer of unknown primary.
• Suitable for treatment with fluoropyrimidine, either alone or in combination with oxaliplatin.
• WHO performance status (PS) 0, 1 or 2 and considered by responsible consultant to be fit to undergo planned chemotherapy and cardiac investigations.
• Baseline laboratory tests (within 1 week prior to starting treatment):
• Neutrophils >1.5 x109 /L and platelet count > 100 x109 /L
• Serum bilirubin <1.5 x upper limit of normal (ULN), alkaline phosphatase <5x ULN, and serum transaminase (either AST or ALT) <3 x ULN
• Estimated glomerular filtration rate (eGFR) >30 mL/min (Patients with eGFR 30-50 mL/min will be included but should be treated at a reduced dose (see master prescription chart).
• For women of childbearing potential; negative pregnancy test and adequate contraceptive precautions.
• Effective contraception for male patients if the risk of conception exists.
• Written informed consent for participation in the trial.

Exclusion Criteria:

• Patients who are unfit for the chemotherapy regimens in this protocol, such as:
• Known intolerance to CAP or other FPs
• Severe uncontrolled concurrent medical illness likely to interfere with protocol treatments
• Poorly controlled angina or MI in previous 6 months
• Any psychiatric or neurological condition which is felt likely to compromise the patient's ability to give informed consent or to comply with oral medication
• Partial or complete bowel obstruction
• Pre-existing neuropathy > grade 1 if combination therapy proposed
• Patients on therapeutic anticoagulation (warfarin or LMWH).
• Patients unable to lie flat.
• Patients unable to withstand the visits and cardiovascular investigations proposed within the study.

Related Conditions & MeSH terms

• Bile Duct Neoplasms
• Cancer of Unknown Primary Site
• Gastrointestinal Cancer
• Gastrointestinal Neoplasms
• Neoplasms, Unknown Primary
• Pancreatic Cancer

Intervention

Drug:
• Teysuno

• Capecitabine

Locations

Country	Name	City	State
United Kingdom	Edinburgh Cancer Centre	Edinburgh	Scotland

Sponsors (2)

Lead Sponsor	Collaborator
University of Edinburgh	NHS Lothian

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary endpoint of the study will be a difference in the duration of ST deviation pre-treatment and during treatment.	This will be recorded using Del Mar Reynolds Lifecard CF/Lifecard 12 recorders, which will record 12 leads over 24 hours and continuously if the storage card is changed daily. Pre-treatment control ECGs will be recorded for 24 hours. Continuous 12-lead monitoring shall be recorded for three days between day 5 and 7 of treatment.	Pre treatment and between day 5-7