跳至主要内容
临床试验/ACTRN12607000146493
ACTRN12607000146493已完成3 期

Trans Tasman Radiation Oncology Group (TROG) 05.01 - Post-Operative Concurrent Chemo-Radiotherapy (Carboplatin) Versus Post-Operative Radiotherapy in High-Risk Cutaneous Squamous Cell Carcinoma of the Head and Neck to improve loco-regional relapse

Trans Tasman Radiation Oncology Group (TROG)0 个研究点目标入组 350 人开始时间: 2007年2月26日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
350

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • 1. Histologically proven Squamous Cell Carcinoma
  • 2. Complete macroscpoic resection of all known disease with or withour microscpoic positive margins. Surgery may consist of one or more of the following:a)Resection of the primary lesion; b) Any type of parotidectomy (superficial, total, partial, etc.); c) Any type of neck dissection(s)
  • 3. High risk feature(s); high risk nodal disease and/or advanced primary disease: a) High Risk Nodal Disease
  • Intra-parotid nodal disease (any number or size, with/without extracapsular extension, with/without an identifiable index lesion)
  • b) Cervical nodal disease with a synchronous index lesion or previously resected cutaneous primary tumour (<5 years) within the corresponding nodal drainage and a mucosal primary has been excluded with at least a Computed Tomography (CT) +/- Magnetic Resonance Imaging (MRI) and panendoscopy*
  • * For cervical nodal disease to be eligible there must be at least one of the following
  • (i) > 2 nodes
  • (ii) largest node > 3cm
  • (iii) Extracapsular extension
  • c) Advanced Primary Disease (Tumor, Node, Metastasis (TNM) 6th Edition 2002) (Appendix 1)
  • T3-4 primary disease (cartilage, skeletal, muscle, bone involvement, >4cm) of the
  • head and neck including lip, nose and external auditory canal with or without nodal
  • d) In transit metastases (metastases between the primary site and the adjoining nodal basin)
  • 4. Age >18 years
  • 5. Written informed consent
  • 6. Eastern Cooperative Oncology Group (ECOG) < 2
  • 7. Absolute neutrophil count > 1.5 X 109/L, platelet count > 100 X 109/L, and haemoglobin > 10g/dL (pre-radiotherapy blood transfusion to elevate the haemoglobin > 10g/dL is permissible)
  • 8. Calculated creatinine clearance (Cockcroft-Gault) >40mL/min
  • 9. Available for follow-up for up to 5 years
  • 10. Life expectancy greater than 6 months.

排除标准

  • 1. Intercurrent illness that will interfere with either the chemotherapy or radiotherapy
  • such as immunosuppression due to medication or medical condition
  • 2. Metastasis(es) below the clavicle
  • 3. Previous radical radiotherapy to the head and neck, excluding treatment of an early glottic cancer > 2 years ago and superficial radiotherapy to cutaneous Squamous Cell Carcinoma (SCC) or basal cell carcinoma
  • 4. High risk for poor compliance with therapy or follow-up as assessed by investigator
  • 5. Pregnant or lactating women
  • 6. Patients with prior cancers, except: those diagnosed > 5 years ago with no evidence of disease recurrence and clinical expectation of recurrence of less than 5%; or
  • successfully treated Level 1 cutaneous melanomas or early glottic cancer > 2 years
  • ago; or non-melanoma skin cancer; or carcinoma in situ of the cervix.
  • 7. Low risk cervical nodal disease* without advanced primary disease
  • *Low risk cervical nodal disease is defined as the presence of all of the following
  • (i) single nodal metastasis,
  • (ii) < 3 cm,
  • (iii) no extracapsular extension.

研究者

发起方
Trans Tasman Radiation Oncology Group (TROG)

相似试验