SOX Regimen as Neoadjuvant Chemotherapy for AJCC Stage II-III Gastric Cancer
Launched by LIN CHEN · Apr 23, 2012
Trial Information
Current as of June 28, 2025
Unknown status
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Histologically confirmed gastric adenocarcinoma
- • 2. Gastroesophageal junction tumour type II or III(NCCN 2009) can be enrolled
- • 3. All patients must undergo EUS,CT(or PET-CT) and laparoscopy to evaluate tumor stage classification (TNM), and only stage II or III (AJCC 7th) gastric cancer patients can be enrolled
- • 4. planning to undergo gastric cancer D2 surgery after neoadjuvant chemotherapy
- • 5. KPS \> 60; ECOG performance status 0-2
- • 6. Life expectancy \> 6 months
- • 7. Age: 20 to 75 years
- • 8. No other severe disease and life expectancy less than five years
- 9. 7 days before enrolled, baseline data should be finished including:
- • Granulocyte count ≥ 1.5×109/L;
- • platelet count ≥ 100×109/L;
- • Hemoglobin ≥ 90g/L;
- • hepatic \< 1.5×ULN;
- • total bilirubin ≤ 1.0×ULN;
- • creatinine \< 1.5×ULN;
- • PT-INR/PTT \< 1.7× ULN
- • 10. Disease had to be measurable by the Response Evaluation Criteria in Solid Tumors (RECIST1.1) criteria
- • 11. Written informed consent and able to comply with the protocol
- Exclusion Criteria:
- • 1. Patient cannot undergo surgery or chemotherapy because of other severe disease
- • 2. Be allergic to chemotherapy drugs
- • 3. Patients receiving any chemotherapy or drugs involved in this trial in four weeks before enrolled
- • 4. Patients received cytotoxic chemotherapy, targeted therapy, immunotherapy or radiotherapy for gastric cancer
- • 5. Within the last 5 years in patients with a history of other malignant diseases
- • 6. Pregnant or breast-feeding women
- • 7. Severe heart disease like symptoms of coronary heart disease, New York Heart Association (NYHA) grade II or worse congestive heart failure or cardiac arrhythmia having medications or myocardial infarction within the last 12 months
- • 8. Patients with upper gastrointestinal obstruction or absorption anomaly; patient in obstruction of the Helicobacter pylori failure like effect S-1 to take and absorb
- • 9. Patients with a history of peripheral nerve disease
- • 10. Patients who get organ transplant
- • 11. lack of dihydropyrimidine dehydrogenase (DPD)
- • 12. Infection or other disease failure to control
About Lin Chen
Lin Chen is a dedicated clinical trial sponsor specializing in the development and oversight of innovative therapeutic solutions. With a focus on advancing medical research, Lin Chen collaborates with healthcare professionals and research institutions to design and implement clinical trials that adhere to the highest standards of regulatory compliance and scientific integrity. Committed to improving patient outcomes, Lin Chen leverages cutting-edge methodologies and a patient-centered approach to facilitate the successful evaluation of new treatments across various medical fields. Through strategic partnerships and a robust infrastructure, Lin Chen aims to accelerate the delivery of safe and effective therapies to the market.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Beijing, , China
Beijing, Beijing, China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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