Apatinib Plus XELOX as Neoadjuvant Therapy in Locally Advanced Gastric Cancer
- Sponsor
- Shanghai Zhongshan Hospital
- Study ID
- NCT03229096
- Phase
- PHASE2
- Status
- Unknown
Conditions
- Chemotherapeutic Toxicity
- Chemotherapy Effect
- Gastric Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Apatinib plus XELOX — DRUGthree weeks is one cycle, 4 cycles followed by radical gastrectomy. Apatinib: 250 mg, p.o., qd, every 3 weeks for the first two cycles. if no level 3 or severer AEs happened, change apatinib to 500mg, p.o.,qd, otherwise keep 250mg in the third cycle. no apatinib in the fourth cycle. Capecitabine: 1000mg/m2, p.o., bid, D1-14, every 3 weeks (treatment for 2 weeks and rest 1 week). Oxaliplatin: 130mg/m2, i.v. over 2h, D1, every 3 weeks.
Study Details
Apatinib plus XELOX regime as Neoadjuvant Therapy in Locally Advanced Gastric Cancer PatientsWith lymph node metastasis
Key Dates
- Start date
- Feb 1, 2017
- Status verified
- Jun 2019
- Primary completion
- Nov 1, 2021
- Completion
- Dec 1, 2021
Study Design
- Enrollment
- 35 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Apatinib plus XELOXPatients will be given the perioperative chemotherapy of Apatinib plus XELOX once recruited
Primary Outcome Measure
Objective response rate (ORR) [ Time Frame: 3 months ]
Central Contacts
- Zhaoqing Tang, MD86-21-64041990
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