Cancer of Lymph Node, Stomach Neoplasms
Conditions
Brief summary
The pattern of lymph node metastasis of the gastric cancer to each geographic lymph nose stations and the relation between each metastasis and survival are to be analyzed by retrospective review of medical records of who enrolled in the CLASSIC trial (NCT00411229) which have compared adjuvant chemotherapy and no adjuvant therapy after radical gastrectomy with extended lymphadenectomy.
Interventions
Sponsors
Saint Vincent's Hospital, Korea
Gachon University Gil Medical Center
Gangnam Severance Hospital
Kyungpook National University Hospital
Kyunghee University Medical Center
Keimyung University Dongsan Medical Center
Korea University Guro Hospital
Korea University Anam Hospital
Kosin University Gospel Hospital
National Cancer Center, Korea
Seoul Veterans Hospital
Seoul National University Bundang Hospital
Soonchunhyang University Hospital
Severance Hospital
Ajou University
Yeungnam University Hospital
Korea Cancer Center Hospital
Ewha Womans University Mokdong Hospital
Chonbuk National University Hospital
Chonnam National University Hospital
Seoul National University Hospital
Study design
Observational model
OTHER
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Criteria of previous CLASSIC trial: Inclusion Criteria: To be eligible for inclusion, each patient must fulfill each of the following criteria: * Ambulatory males or females, aged ≥18 years. * Karnofsky performance status of ≥70 %. * Histologically confirmed gastric adenocarcinoma, staged pathologically, AJCC/UICC stage II (T2N1, T1N2, T3N0), IIIa (T3N1, T2N2, T4N0), and IIIb (T3N2). At least 15 examined lymph nodes are required to ensure the adequate TNM classification) * Patients who underwent curative D2 lymphadenectomy resection for gastric cancer with no macroscopic or microscopic evidence for remaining tumor, who can be randomized to either study arm within 6 weeks after surgery. * Give written informed consent prior to study specific screening procedures, with the understanding that the patient has the right to withdraw from the study at any time, without prejudice.
Exclusion criteria
Patients who fulfill any of the following criteria will be excluded: * Serious concomitant medical illnesses that would limit life expectancy to \< 5 years. * Pregnant or lactating women. * Women of childbearing potential with either a positive or no pregnancy test at baseline. Postmenopausal women must have been amenorrheic for at least 12 months to be considered of non-child bearing potential. * Sexually active males and females (of childbearing potential) unwilling to practice contraception during the study. * Any evidence of metastatic disease (including presence of tumor cells in the ascites). * Previous cytotoxic chemotherapy, radiotherapy or immunotherapy except corticosteroids, for the currently treated gastric cancer. * History of another malignancy within the last five years except cured basal cell carcinoma of skin and cured carcinoma in-situ of uterine cervix. * History of uncontrolled seizures, central nervous system disorders or psychiatric disability judged by the Investigator to be clinically significant precluding informed consent or interfering with compliance for oral drug intake. * Clinically significant (i.e. active) cardiac disease e.g. symptomatic coronary artery disease, New York Heart Association (NYHA) grade II or greater congestive heart failure or serious cardiac arrhythmia requiring medication or myocardial infarction within the last 12 months. * Lack of physical integrity of the upper gastrointestinal tract or those who have malabsorption syndrome likely to influence absorption of capecitabine, or inability to take oral medication. * Known peripheral neuropathy ≥ CTCAEv3 grade 1. Absence of deep tendon reflexes (DTRs) as the sole neurologic abnormality does not render the patient ineligible. * Organ allografts requiring immunosuppressive therapy. * Serious uncontrolled intercurrent infections or other serious uncontrolled concomitant disease.- * Moderate or severe renal impairment \[creatinine clearance equal to or below 50 ml/min (calculated according to Cockroft and Gault)\], or serum creatinine \> 1.5 x upper limit of normal (ULN). * Any of the following laboratory values: * Absolute neutrophil count (ANC) \< 1.5 x 10\^9/L * Platelet count \< 100 x 10\^9/L * Total bilirubin \> 1.5 x ULN * ALAT, ASAT \> 2.5 x ULN * Alkaline phosphatase \> 2.5 x ULN. * Prior unanticipated severe reaction to fluoropyrimidine therapy (with or without documented DPD deficiency) or patients with Kknown dihydropyrimidine dehydrogenase (DPD) deficiency. * Hypersensitivity to platinum compounds or any of the components of the study medications. * Received any investigational drug or agent/procedure, i.e. participation in another trial, within 4 weeks before randomization. * Blood transfusions or growth factors to aid hematologic recovery within 2 weeks prior to study treatment start. * Requirement for concurrent use of the antiviral agent sorivudine (antiviral) or chemically related analogues, such as brivudine. * Unwilling or unable to comply with the protocol for the duration of the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Topographic pattern of metastasis to regional lymph node stations | at the time of surgery |
Secondary
| Measure | Time frame |
|---|---|
| survival according to the metastatic lymph node station | 3 and 5years |
| survival according to lymph node ratio | 3 and 5years |
| recurrence pattern | 3 and 5years |
Outcome results
None listed