CTRI/2023/04/051617已完成2 期
eoadjuvant Chemo-Immunotherapy using Carboplatin, Paclitaxel, Oral Metronomic Chemotherapy and Low Dose Nivolumab for Locally Advanced Borderline Resectable ? Oral Cavity squamous cellcarcinoma - A Prospective Study - NeoLOCUS
CMC Vellore Fluid Research Grant0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Inclusion Criteria: Patients with newly diagnosed Locally Advanced Oral Cavity cancers fitting the below criteria:
- •1. Adults more than 18 years of age with ECOG Performance Status 0-1
- •2. Clinical AJCC Eighth edition stage III to IVB
- •3. Biopsy-proven Oral cavity squamous cell carcinoma
- •4. Deemed Borderline Resectable ? in MDT
- •5. Written informed consent obtained from subject or subject’s legal representative and ability for subject to comply with the requirements of the study
- •6. Required initial laboratory parameters:
- •Neutrophils more than 1,500/cu.mm; Platelets more than 100,000/cu.mm; Hemoglobin more than 8g/dl; Estimated creatinine clearance more than 30 ml/min (Cockcroft Gault formula)
排除标准
- •1. Pregnant, breastfeeding, or unwilling to practice birth control during participation in the study
- •2. Prior treatment with chemotherapy, surgery, or radiation therapy for the current oral cavity cancer
- •3. Major surgical procedure within 28 days prior to randomization or anticipation of need for major surgery during the course of study other than that required for the cancer treatment itself
- •4. Documented baseline neuropathy CTCAE v5.0 grade 2 or worse
- •5. Patients with congestive heart failure symptomatic NYHA class III or worse
- •6. Pre-treatment documented LV dysfunction and/or ejection fraction less than 50%
研究者
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