Pharmacokinetic Study of Capecitabine After Total Gastrectomy for Stomach Adenocarcinoma

Adenocarcinoma of the Stomach Clinical Trial

Official title:

A Pharmacokinetic Study of Capecitabine in Patients Undergoing Peri-operative Chemotherapy and a Total Gastrectomy for Adenocarcinoma of the Stomach

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00871273
• Other study ID #: CAP002
• Status: Terminated
• Phase: Phase 4
• First received: March 27, 2009
• Last updated: July 18, 2015
• Start date: November 2009
• Est. completion date: October 2014

Study information

• Verified date: July 2015
• Source: Cambridge University Hospitals NHS Foundation Trust
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the pharmacokinetics (PK) of capecitabine in patients who have undergone a total gastrectomy.

Description:

Primary Objective:

• To establish the pharmacokinetics (PK) of capecitabine in patients who have undergone a total gastrectomy

Secondary Objectives:

• To compare the pharmacokinetic profile of capecitabine administered to patients with gastric cancer pre- and post-gastrectomy and to compare this to historical data of capecitabine PK values in patients with other cancer types.

• To ensure equivalent capecitabine exposure when compared to PK data from the same patients prior to gastrectomy.

This is a clinical trial to evaluate the pharmacokinetics (PK) of capecitabine in patients who have undergone a total gastrectomy. The study also aims to establish the toxicity profile of capecitabine in these patients, to identify any dose limiting toxicities (DLT), and to ensure equivalent capecitabine exposure when compared to PK data from the same patients prior to gastrectomy. Screening tests will consist of demographic details, complete medical history, physical exam, vital signs, tumour serum markers, haematology and biochemistry tests. There will also be an ECG, chest X-Ray or CT thorax, CT abdomen and a serum or urine pregnancy test (for women of childbearing potential). Haematology and Biochemistry will be repeated prior to each study drug administration. All patients will receive 6 cycles of oral capecitabine chemotherapy at a dose of 625 mg/m2, administered twice daily at 12 hourly intervals for 21 consecutive days. Total proposed duration of therapy is 3 cycles pre-operatively and 3 cycles post-operatively. Capecitabine and its metabolites (DFCR, DFUR and 5-FU) plasma levels will be measured during the 1st and 4th cycles in all patients. Treatment should continue for 6 cycles unless there is evidence of disease progression, or unacceptable toxicity.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 13
• Est. completion date: October 2014
• Est. primary completion date: October 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients must have histologically confirmed gastric carcinoma suitable for potentially curative resection.

• Surgery must be planned to involve a total gastrectomy.

• No concurrent mechanical or malabsorptive disorders precluding affective oral administration of the drug (excluding early satiety related to the presence of the malignancy).

• Age = 18 years.

• World Health Organisation (WHO) performance status of = 2 (Appendix 1).

• Haematological and biochemical indices (These measurements must be performed within one week prior to the patient going on study.)

• Haemoglobin (Hb) = 9.0 g/dl

• Neutrophils = 1.5 x 109/L

• Platelets (Plts) = 100 x 109/L

• Serum bilirubin = 1.5 x upper normal limit

• Alanine amino-transferase (ALT) and / or aspartate amino-transferase (AST) = 2.0 x upper limit of normal (ULN). (If both are measured, both must be = 2.0 x ULN)

• Calculated creatinine clearance = 50 ml/min (uncorrected value) or isotope clearance measurement = 50ml/min

• Female patients of child-bearing potential must have a negative serum or urine pregnancy test prior to enrolment and agree to use appropriate medically approved contraception for four weeks prior to entering the trial, during the trial, and for six months afterwards.

• Male patients must agree to use appropriate medically approved contraception during the trial and for six months afterwards.

• Written, informed consent provided.

• Ability of the patient to co-operate with treatment and follow up must be ensured.

• Patients receiving oral anti-coagulation prior to entry into the study, must be converted to low molecular weight heparin in light of the interaction between capecitabine and warfarin.

Exclusion Criteria:

• Patients with gastric lymphoma or other histological diagnosis

• Any evidence of malignant ascites, peritoneal or liver metastasis, spread to other distant abdominal or extra-abdominal organs.

• History of confirmed Ischaemic Heart Disease, concurrent congestive heart failure or prior history of class III / IV cardiac disease (Appendix 2 - New York Heart Association (NYHA) Scale)

• Concurrent mechanical or malabsorptive disorders precluding effective oral administration of the drug

• Use of other concomitant chemotherapy

• Pregnancy or Lactation

• Patients known to be serologically positive for Hepatitis B, Hepatitis C or Human Immunodeficiency Virus (HIV).

• Patients who are high medical risks because of non-malignant systemic disease including active uncontrolled infection.

• Any other serious medical or psychological condition precluding adjuvant treatment

• Patients with any other condition which in the Investigator's opinion would not make the patient a good candidate for the clinical trial.

Study Design

Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science

Related Conditions & MeSH terms

• Adenocarcinoma
• Adenocarcinoma of the Stomach

Intervention

Drug:
• capecitabine
film-coated tablet 1250 mg/m2 twice daily 14 days for 14 days. Number of cycles: 3 cycles pre-operatively and 3 cycles post-operatively unless there is evidence of disease progression on chemotherapy

Locations

Country	Name	City	State
United Kingdom	Cambridge University Hospitals NHS Foundation Trust, University of Cambridge Oncology Centre	Cambridge
United Kingdom	Edinburgh Cancer Centre, Western General Hospital	Edinburgh

Sponsors (1)

Lead Sponsor	Collaborator
Cambridge University Hospitals NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To establish the pharmacokinetics (PK) of capecitabine in patients who have undergone a total gastrectomy.		Samples collected predose and 0.25, 0.5, 1, 2, 3, 4, 5, 6, 8, and 24 hours on day 1 of cycles 1 and 4	No
Secondary	To compare the pharmacokinetic profile of capecitabine administered to patients with gastric cancer pre- and post-gastrectomy and to compare this to historical data of capecitabine PK values in patients with other cancer types.		1 year	No
Secondary	To ensure equivalent capecitabine exposure when compared to PK data from the same patients prior to gastrectomy.		1 Year	No