Upfront Surgery Vs Induction Chemotherapy Followed By Surgery In Oral Cavity Squamous Cell Cancers With Advanced Nodal Disease (SurVIC Trial): A Phase 3 Multicentric Randomized Controlled Trial
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 300
- 试验地点
- 7
- 主要终点
- To study the 2 year disease free survival by adding induction chemotherapy before surgery in patients of oral cancer with advanced nodal disease as compared to upfront surgery.
研究概览
简要总结
| Title |
Upfront Surgery Vs Induction Chemotherapy Followed By Surgery In Oral Cavity Squamous Cell Cancers With Advanced Nodal Disease (SurVIC Trial): A Phase 3 Multicentric Randomized Controlled Trial
|Rationale and Knowledge gap
Majority of oral cancers in India present in the advanced stage hence tend to have poor oncological outcomes. Chemotherapy has been associated with improved oncological outcomes in various cancers, but its role in oral cancer is still not well defined in curative settings, beyond radio sensitization. Attempted trials of Neoadjuvant chemotherapy failed to show oncological advantage despite an excellent response rate, in part due to poor patient selection. Patients with a biologically aggressive disease are more likely to benefit, hence we intend to find out the oncological advantage of adding induction chemotherapy to oral squamous cell cancer with advanced nodal disease (N2-N3).
|Novelty
Earlier studies suffered from their heterogeneous patient population- all head and neck subsites together and included either inoperable cancer/ early-stage operable cases. Due to such patient selection, the intended results were never met. The current study is intended to study the role of chemotherapy in curable patients who are most likely to benefit (biologically aggressive and advanced stage of presentation).
|Objective
Primary:
â— To study the 2 year disease free survival by adding induction chemotherapy before surgery in patients of oral cancer with advanced nodal disease as compared to upfront surgery.
Secondary:
â— To assess treatment related outcomes between the treatment arms- Response rate; Treatment compliance; treatment related toxicity, postoperative complications and Quality of life.
â— To study the overall survival at 2 years.
â— Oral cancer tissue biobanking for future translational research.
|Study population
Operable Oral cavity Squamous cell carcinoma with advanced nodal disease (N2-N3)
|Study Design
Open label, Multi centric, randomized controlled trial with allocation ratio of 1:1
|Study
Sites
Leading Center: AIIMS Jodhpur
Collaborating Centers:
1. AIIMS Bhubaneswar
2. AIIMS Rishikesh
3. AIIMS Bathinda
4. King’s George Medical university Lucknow
5. Shri Mahant Indiresh Hospital, Dehradun
6. Geetanjali Medical College, Udaipur
|Sample Size
The primary end point is disease-free survival. In order to have 80% power to detect a hazard ratio of 0.67, using a two-sided significance level, a total of 184 events are needed. Assuming an accrual rate of 15 patients a month, 300 patients need to be recruited. The analysis of DFS will take place 32 months after the start of the trial. The follow-up of patients will continue for 5 years. The analysis of OS will be conducted when 184 deaths are observed.
|Inclusion Criteria
Biopsy proven, operable oral Squamous cell carcinoma cT1-T4; cN2-N3, with adequate organ function, Age- 18-75 years, ECOG-PS:0-2
|Treatment Arms
Standard Arm (SURG arm):
Surgery (Wide local Excision/composite resection with neck dissection) followed by adjuvant Radiotherapy ± Concurrent Chemotherapy
Experimental Arm (ICT):
2# TPF based induction chemotherapy followed by Surgery (Wide local Excision/composite resection with neck dissection) followed by adjuvant Radiotherapy ± Concurrent Chemotherapy
|Study endpoints
Primary- Disease free survival
Secondary- Overall survival/ Quality of life/ Toxicity of treatment/ Treatment tolerance
|Study duration
1. Preparation/ site initiation/IEC clearances/ MOUs- 3 Months
2. Participants accrual- 24 Months
3. Follow up and trial completion report- 9 Months
4. Follow up for Overall survival- 24 Months
|Feasibility
As per past institutional experience, we expect to enrol the desired number of cases in 2 years. The approximate number of case accrual per centre is as follows-
â— AIIMS Jodhpur- 50/ year
◠King’s George Medical university Lucknow- 40 patients/ year
â— AIIMS Bhubaneswar- 25 patients/ year
â— AIIMS Rishikesh- 25 patients/ year
â— AIIMS Bathinda- 20 patients/ year
â— Shri Guru Ram Rai Institute of medical and Health Sciences & Shri Mahant Indiresh Hospital, Dehradun- 20 patients/ year
â— Geetanjali Medical College, Udaipur- 20 patients/ year
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 75.00 Year(s)(—)
- 性别
- All
入选标准
- •Biopsy proven, operable oral Squamous cell carcinoma cT1-T4; cN2-N3, with adequate organ function, Age- 18-75 years, ECOG-PS:0-2.
排除标准
- •Pregnant, History of moderate to severe hearing loss, History of previous malignancy excluding non-melanoma skin cancers or cervical carcinoma in situ, Documented Weight loss of more than 15% in the last 6 months, or Patients with known HIV, hepatitis B or C infection.
结局指标
主要结局
To study the 2 year disease free survival by adding induction chemotherapy before surgery in patients of oral cancer with advanced nodal disease as compared to upfront surgery.
时间窗: 2 Years
次要结局
- Oral cancer tissue biobanking for future translational research.
- To assess treatment related outcomes between the treatment arms- Response rate; Treatment compliance; treatment related toxicity, postoperative complications & Quality of life.(3 Months)
- To study the overall survival at 2 years.(2 Years)
- Oral cancer tissue biobanking for future translational research.(NA)
研究者
Dharma Ram Poonia
AIIMS Jodhpur
