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Chemotherapy With or Without Bevacizumab or Lapatinib to Treat Operable Oesophagogastric Cancer

Phase 2
Conditions
Oesophagogastric Cancer
Interventions
Biological: bevacizumab
Procedure: adjuvant therapy
Procedure: neoadjuvant therapy
Procedure: conventional surgery
Registration Number
NCT00450203
Lead Sponsor
Professor David Cunningham
Brief Summary

RATIONALE: Drugs used in chemotherapy, such as epirubicin, cisplatin, and capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as bevacizumab, and small molecule tyrosine kinase inhibitors, such as lapatinib, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Lapatinib targets a specific growth receptor, HER-2. Chemotherapy together with bevacizumab or lapatinib, in HER-2 positive tumours, may kill more tumor cells.

PURPOSE: This randomized phase II/III trial is studying the side effects and how well giving combination chemotherapy together with bevacizumab works compared with combination chemotherapy alone in treating patients with previously untreated stomach cancer, gastroesophageal junction cancer or lower oesophageal cancer that can be removed by surgery. The feasibility study is studying the safety of adding lapatinib to chemotherapy in patients with HER-2 positive previously untreated stomach cancer, gastroesophageal junction cancer or lower oesophageal cancer that can be removed by surgery. The feasibility study will also assess the feasibility of timely HER-2 testing and estimate the HER-2 positivity rate in this patient population.

Detailed Description

OBJECTIVES:

Primary

* Assess the safety and efficacy of neoadjuvant and adjuvant chemotherapy comprising epirubicin hydrochloride, cisplatin, and capecitabine with or without bevacizumab in patients with previously untreated, resectable gastric, gastroesophageal junction or lower oesophageal cancer.

* Assess the safety of neoadjuvant and adjuvant chemotherapy comprising epirubicin hydrochloride, cisplatin, and capecitabine with or without lapatinib in patients with HER-2 positive previously untreated, resectable gastric, gastroesophageal junction or lower oesophageal cancer.

OUTLINE: This is a multicenter, randomized, open-label, controlled study. Patients are randomized to 1 of 4 treatment arms.

* Arm I and II: Patients receive epirubicin hydrochloride IV and cisplatin IV over 4 hours on day 1 and capecitabine orally twice daily on days 1-21. Treatment repeats every 21 days for up to 3 courses in the absence of disease progression or unacceptable toxicity.

Patients undergo surgery 5-6 weeks after completion of chemotherapy. Patients then receive 3 additional courses of chemotherapy beginning 6-10 weeks after surgery.

* Arm II: Patients receive bevacizumab IV over 30-90 minutes, epirubicin hydrochloride IV, and cisplatin IV over 4 hours on day 1 and capecitabine orally twice daily on days 1-21. Treatment repeats every 21 days for up to 3 courses in the absence of disease progression or unacceptable toxicity.

Patients undergo surgery 5-8 weeks after completion of chemotherapy. Patients then receive 3 additional courses of chemotherapy and bevacizumab beginning 6-10 weeks after surgery. Patients then receive maintenance therapy comprising bevacizumab IV over 30-90 minutes on day 1. Maintenance therapy repeats every 21 days for up to 6 courses in the absence of disease progression or unacceptable toxicity.

* Arm IV: Patients receive lapatinib orally once daily, epirubicin hydrochloride IV, and cisplatin IV over 4 hours on day 1 and capecitabine orally twice daily on days 1-21. Treatment repeats every 21 days for up to 3 courses in the absence of disease progression or unacceptable toxicity.

Patients undergo surgery 5-8 weeks after completion of chemotherapy. Patients then receive 3 additional courses of chemotherapy and lapatinib beginning 6-10 weeks after surgery. Patients then receive maintenance therapy comprising lapatinib orally once daily on days 1-21. Maintenance therapy repeats every 21 days for up to 6 courses in the absence of disease progression or unacceptable toxicity.

Quality of life is assessed at baseline, during treatment, and during the follow-up period.

After completion of study treatment, patients are followed at 9, 18, and 27 weeks after the start of course 4, 1 year post surgery, every 6 months for 2 years, and then annually thereafter.

PROJECTED ACCRUAL: A total of 1063 patients were recruited to the bevacizumab comparison of the study (now closed to recruitment) and 40 patients with HER-2 positive tumours will be recruited into the ST03 feasibility study.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
1103
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Epirubicin, Cisplatin and Capecitabineneoadjuvant therapyECX chemotherapy
ECX + LapatinibEpirubicinECX + Lapatinib
ECX + Bevacizumabconventional surgeryECX + Bevacizumab
ECX + Bevacizumabneoadjuvant therapyECX + Bevacizumab
ECX + Lapatinibadjuvant therapyECX + Lapatinib
ECX + BevacizumabbevacizumabECX + Bevacizumab
ECX + Bevacizumabadjuvant therapyECX + Bevacizumab
Epirubicin, Cisplatin and Capecitabineadjuvant therapyECX chemotherapy
Epirubicin, Cisplatin and Capecitabineconventional surgeryECX chemotherapy
ECX + Lapatinibconventional surgeryECX + Lapatinib
ECX + Lapatinibneoadjuvant therapyECX + Lapatinib
ECX + BevacizumabcapecitabineECX + Bevacizumab
ECX + BevacizumabcisplatinECX + Bevacizumab
ECX + BevacizumabEpirubicinECX + Bevacizumab
Epirubicin, Cisplatin and CapecitabinecisplatinECX chemotherapy
Epirubicin, Cisplatin and CapecitabinecapecitabineECX chemotherapy
Epirubicin, Cisplatin and CapecitabineEpirubicinECX chemotherapy
ECX + LapatinibcapecitabineECX + Lapatinib
ECX + LapatinibcisplatinECX + Lapatinib
ECX + LapatinibLapatinibECX + Lapatinib
Primary Outcome Measures
NameTimeMethod
Overall survivalend of trial
Safetyat the end of phase II and phase III
Efficacyend of trial
Secondary Outcome Measures
NameTimeMethod
Treatment-related morbidityend of trial
Feasibilityend of trial
Surgical resection ratesend of trial
Cost-effectivenessend of trial
Quality of lifeend of trial
Response rates to pre-operative treatmentat phase II review and at end of trial
Disease-free survivalend of trial
HER-2 Positivity RateEnd of trial
Feasibility of centralised HER-2 testingAfter 60 patients tested and then after 110 patients tested and then at end of trial

Trial Locations

Locations (41)

Bristol Haematology and Oncology Centre

🇬🇧

Bristol, England, United Kingdom

Huddersfield Royal Infirmary

🇬🇧

Huddersfield, West Yorks, England, United Kingdom

Cumberland Infirmary

🇬🇧

Carlisle, England, United Kingdom

Rochdale Infirmary

🇬🇧

Rochdale, England, United Kingdom

Royal Bournemouth Hospital

🇬🇧

Bournemouth, England, United Kingdom

Bradford Royal Infirmary

🇬🇧

Bradford, England, United Kingdom

Addenbrooke's Hospital

🇬🇧

Cambridge, England, United Kingdom

Doncaster Royal Infirmary

🇬🇧

Doncaster, England, United Kingdom

Leeds Cancer Centre at St. James's University Hospital

🇬🇧

Leeds, England, United Kingdom

St. Luke's Cancer Centre at Royal Surrey County Hospital

🇬🇧

Guildford, England, United Kingdom

Lincoln County Hospital

🇬🇧

Lincoln, England, United Kingdom

Aintree University Hospital

🇬🇧

Liverpool, England, United Kingdom

Saint Bartholomew's Hospital

🇬🇧

London, England, United Kingdom

St. George's Hospital

🇬🇧

London, England, United Kingdom

St. Mary's Hospital

🇬🇧

London, England, United Kingdom

Mid Kent Oncology Centre at Maidstone Hospital

🇬🇧

Maidstone, England, United Kingdom

Christie Hospital

🇬🇧

Manchester, England, United Kingdom

Clatterbridge Centre for Oncology

🇬🇧

Merseyside, England, United Kingdom

Northern Centre for Cancer Treatment at Newcastle General Hospital

🇬🇧

Newcastle-Upon-Tyne, England, United Kingdom

Derriford Hospital

🇬🇧

Plymouth, England, United Kingdom

Berkshire Cancer Centre at Royal Berkshire Hospital

🇬🇧

Reading, England, United Kingdom

Dorset Cancer Centre

🇬🇧

Poole Dorset, England, United Kingdom

Salisbury District Hospital

🇬🇧

Salisbury, England, United Kingdom

Southampton General Hospital

🇬🇧

Southampton, England, United Kingdom

Wexham Park Hospital

🇬🇧

Slough, Berkshire, England, United Kingdom

Royal Marsden - Surrey

🇬🇧

Sutton, England, United Kingdom

Aberdeen Royal Infirmary

🇬🇧

Aberdeen, Scotland, United Kingdom

Velindre Cancer Center at Velindre Hospital

🇬🇧

Cardiff, Wales, United Kingdom

Basingstoke and North Hampshire Hospital

🇬🇧

Basingstoke, United Kingdom

Birmingham Heartlands Hospital

🇬🇧

Birmingham, United Kingdom

University Hospitals Coventry and Warwickshire

🇬🇧

Coventry, United Kingdom

Beatson West of Scotland Cancer Centre

🇬🇧

Glasgow, United Kingdom

Leicester Royal Infirmary

🇬🇧

Leicester, United Kingdom

Norfolk and Norwich University Hospital

🇬🇧

Norwich, United Kingdom

Churchill Hospital

🇬🇧

Oxford, United Kingdom

St James Hospital

🇬🇧

Leeds, United Kingdom

Queens Hospital

🇬🇧

Romford, United Kingdom

Great Western Hospital

🇬🇧

Swindon, United Kingdom

Weston Park

🇬🇧

Sheffield, United Kingdom

Musgrove Park Hospital

🇬🇧

Taunton, United Kingdom

Castle Hill Hospital

🇬🇧

Cottingham, United Kingdom

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