EUCTR2005-005464-92-DE
Active, not recruiting
Not Applicable
A randomized phase II study of docetaxel in combination with oxaliplatin with or without 5-FU or capecitabine in metastatic or locally recurrent gastric cancer previously untreated with chemotherapy for advanced disease. - DOCOX GASTRIC (Docetaxel-Oxaliplatin in Gastric Cancer)
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Sanofi-aventis groupe
- Enrollment
- 270
- Status
- Active, not recruiting
- Last Updated
- 13 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patient’s consent form obtained, signed and dated before beginning specific protocol procedures.
- •2\.Histologically proven gastric adenocarcinoma, including adenocarcinoma of the gastro\-oesophageal junction,
- •3\.Metastatic or locally recurrent disease
- •4\.Prior adjuvant (and/or neo\-adjuvant) chemotherapy with 5\-FU, CDDP, epirubicin is allowed provided that the patient has relapsed \> 12 months after the end of the chemotherapy.
- •5\.At least 4 weeks from prior radiotherapy for palliation of metastases and 3 weeks from surgery.
- •6\.Patient age \= 18
- •7\.Performance status Karnofsky index \> 70
- •8\.Hematology within 7 days before randomization:
- •Hb \=10g/dl, ANC \=2\.0 109/L, platelets \=100 x 109/L
- •9\.Blood chemistry within 7 days before randomization:
Exclusion Criteria
- •Patients will be excluded from this study if they meet any of the following criteria:
- •1\.Other tumor type than adenocarcinoma
- •2\.Any prior palliative chemotherapy.
- •3\.Any prior adjuvant (and/or neo\-adjuvant) chemotherapy other than those specified in inclusion criterion \#4\.
- •4\.No prior Taxotere® or Eloxatin® or Xeloda®
- •5\.Neurosensory symptoms NCI\-CTCAE grade\=2
- •6\.Prior radiotherapy other than (neo) adjuvant. In case of (neo)adjuvant radiotherapy, the relapse must be outside the radiotherapy fields
- •7\.Previous or other current malignancies, with the exception of adequately treated in situ carcinoma of the cervix uteri or non melanoma skin cancer and of (any) cancers cured more than 5 years before study entry
- •8\.Other serious illness or medical conditions:
- •\-unstable cardiac disease despite treatment, myocardial infarction within 6 months prior to study entry,
Outcomes
Primary Outcomes
Not specified
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