Eligibility Details:
Inclusion Criteria:
Arm 1:
- Patients with suspected or histologically confirmed localized gastroesophageal
adenocarcinoma amenable to curative intent therapy with surgery as standard of care,
either with or without induction chemotherapy or chemo radiotherapy.
- Age ≥18 years.
- Eastern Cooperative Group (ECOG) performance status 0-2
Arm 2
- Patients must have a histological or radiological diagnosis of advanced
gastroesophageal cancer.
- Patient must have a tumour lesion that is amenable to a core needle biopsy as judged
by a staff radiologist. A minimum of 3 x 18G good quality tumour cores must be safely
obtainable under CT or US guidance. Biopsy to be completed before systemic therapy
begins.
- Patients must have a measurable lesion by RECIST 1.1 in addition to the lesion that is
going to be biopsied. See Section 13.1.3 for the evaluation of measurable disease.
Patients with locally advanced gastroesophageal cancer with no metastatic disease who
are not candidates for curative intent therapy as per part 1 of the protocol, are
eligible for part 2 and are exempt from this criterion.
- Patients must be fit enough to safely undergo a tumour biopsy as judged by the
investigator.
- Age ≥ 18 years.
- Eastern Cooperative Group (ECOG) performance status 0-2
- Life expectancy of greater than 90 days, as judged by the investigator.
- Patients plan to undergo systemic treatment with platinum-based chemotherapy (e.g.
FOLFOX, CF, CX with or without Herceptin) as first line standard systemic palliative
treatment, or as part of a first line clinical trial.
- Within 14 days of the proposed biopsy date, patients must have normal organ and marrow
functions.
Exclusion Criteria:
Arm 1
- Patients who are planned for definitive chemoradiation without surgical resection will
be excluded from this study.
- Any other condition that would, in the Investigator's judgment, contraindicate the
patient's participation in the clinical study due to safety concerns or compliance
with clinical study procedures.
Arm 2
- Patients with one or more contraindications to tumour biopsy according to UHN's
standard biopsy procedures.
- Patients who had prior systemic treatment for advanced or metastatic gastroesophageal
cancer.
- Patients who are currently on anti-cancer treatment including chemotherapy for another
malignancy.
- Patients with known brain metastases are excluded from participation in this clinical
study.
- Patients with advanced gastroesophageal cancer who are going to be treated with
non-platinum based chemotherapy in the first line setting.
- Uncontrolled inter-current illness including, but not limited to, ongoing or active
infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia, or psychiatric illness/social situations that would limit compliance with
study requirements.
- Any condition that would, in the investigators' judgment, contraindicate the patient's
participation in the clinical study due to safety concerns or compliance with clinical
study procedures.
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