Tracheal Replacement Using A Cryopreserved Aortic Allograft For R0 Resection In Locally Advanced Thyroid Cancer (TRITON 02 Tracheal Replacement In ThyrOid caNcer) (TRITON 02)
Airway transplantation remains a great surgical and biological challenge. This is still an unsolved problem for patients in therapeutic impasse because of major tracheobronchial lesions requiring surgical resection and airway reconstruction. Schematically, 5 principal ways of research have been explored with the use of synthetic prostheses, airway bio-prostheses, tracheal allografts, various autologous substitutes and more recently bio-engineered conduits. The lack of prospective human studies did not allow standardizing surgical approaches. Since 1997, airway bioengineering using aortic grafts as biological matrices, has been tested in our laboratory (Alain Carpentier Foundation) as a potential solution to the unsolved problem of tracheobronchial replacement. Preclinical studies showed that autologous aortic grafts, fresh and cryopreserved aortic allografts could be valuable tracheobronchial substitutes. The progressive regeneration of both epithelium and cartilage within the aortic matrices from recipient progenitor/stem cell homing permitted the restoration of new functional airways. These results allowed clinical applications in patients with extensive tracheal diseases or lung neoplasms. Recently the feasibility of this innovative approach using stented -80°C CAA was demonstrated in a prospective study including 20 patients (NCT01331863; Martinod E et al. Feasibility of bioengineered tracheal and bronchial reconstruction using stented aortic matrices. JAMA 2018;319:2212-22).
Two patients included in the series had a locally advanced thyroid cancer with a tracheal invasion. With a maximal follow-up of 2 years and 7 months, there was no complication related to surgery and no recurrence of thyroid cancer. De novo generation of cartilage within the aortic matrices allowed stent removal in both patients. Since the JAMA publication, a new prospective observational study using the same methodology has restarted on March 2019. Of the 7 new patients included, 2 had recurrent or extended thyroid cancer. Thus, 4 patients with thyroid cancer and tracheal invasion received this innovative approach of airway bioengineering using a stented cryopreserved aortic allograft. The survival of differentiated thyroid cancers is directly conditioned by a complete surgical resection and the absence of residual cancer or recurrence in the tracheal and/or esophageal wall. Locally invasive disease from differentiated thyroid cancer represents 13% to 15% of patients. T4 locally-advanced thyroid cancer includes gross extrathyroidal extension into major neck structures; T4a gross extrathyroidal extension invading subcutaneous soft tissues, larynx, trachea, esophagus or recurrent laryngeal nerve from a tumor of any size; T4b gross extrathyroidal extension invading prevertebral fascia or encasing carotid artery or mediastinal vessels from a tumor of any size. Papillary thyroid carcinoma represents the most common type of differentiated thyroid cancer associated with extrathyroidal spread. Invasion of local structures most commonly involves the strap muscles, recurrent laryngeal nerve, and trachea. Extrathyroidal spread may also affect the larynx, esophagus, and major vessels, although this is rare. Finally, 50% of all deaths are due to tracheal invasion that is poorly managed or not treated early. The incidence of these invasions is probably underestimated, reaching between 1 and 20% of patients operated for a differentiated cancer of the thyroid. Only radical surgery can improve the prognosis. No other current treatment (radiotherapy, chemotherapy) can be considered as curative. There is no recommendation for the treatment of these invasions (abstention, shaving, tracheal resection with direct anastomosis, pharyngo-laryngectomy) and therapeutic decisions are left to the discretion of the teams and their medical/surgical expertise. This study propose to evaluate the use of an innovative approach in patients with locally advanced thyroid cancer to provide a R0 surgical resection and then a better prognosis. The use of this approach could be proposed in case of incomplete resection after thyroidectomy, redo surgery, recurrence especially if there is a vocal cord paralysis and extensive tracheal invasion. This is the first known study proposing to evaluate a new approach for patients with extended thyroid cancer invading the trachea. In fact, this group of patients is usually referred to a palliative treatment including local therapy, radiotherapy and more rarely chemotherapy.
研究概览
地位
条件
详细说明
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:Emmanuel MARTINOD, Pr
- 电话号码:+33148955231, +33689785327
- 邮箱:emmanuel.martinod@aphp.fr
研究联系人备份
- 姓名:Christophe TRESSALLET, Pr
- 电话号码:+33148955231
学习地点
-
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Île-de-France Region
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Bobigny、Île-de-France Region、法国、93009 Bobigny Cedex
- Hopital Avicenne
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
Study inclusion criteria will be approved by a multidisciplinary tumor board (local or national, e.g., TUTHYREF, if necessary) and will include the following:
- patients with thyroid cancer involving the trachea and/or cricoid cartilage that is not amenable to simple resection-anastomosis, regardless of prior treatment status;
- patients with any histological type of thyroid cancer, excluding the undifferentiated/anaplastic type;
- patients deemed eligible for surgical resection based on standard preoperative assessment;
- lesions considered unresectable via standard procedures;
- women using effective contraception throughout the study duration, in accordance with CTCG recommendations.
Exclusion Criteria:
- age under 18 years;
- patients unable to provide consent;
- patients not covered by the French Social Security system;
- patients with undifferentiated/anaplastic thyroid cancer;
- patients for whom standard preoperative assessment precludes surgical resection (e.g., severe malnutrition, limiting cardiovascular disease, limiting respiratory disease with DLCO < 35% or VO2max < 10 ml/min/kg);
- patients with *de novo* thyroid cancer and minimal tracheal invasion suitable for simple resection-anastomosis;
- patients with *RET* mutations;
- pregnant or breastfeeding women;
- patients participating in another interventional study;
- patients under legal guardianship or trusteeship. Note that for patients with metastatic disease, the decision regarding inclusion or exclusion will be made on a case-by-case basis during the multidisciplinary team (MDT) meeting; contraindications to standardized tracheal resection and primary anastomosis reconstruction will be determined by the MDT; and all histological types-including medullary carcinoma-will be included, with the exception of undifferentiated/anaplastic types, to ensure a homogeneous group regarding local invasion and prognosis. Note also that minimal invasion (<2 cm)-in the absence of repeat surgery, and regardless of the presence or absence of recurrent laryngeal nerve paralysis-requires resection-anastomosis.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Surgery
Surgical resection using the innovative approach
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Resection and replacement of the invaded tracheal segment with a cryopreserved aortic allograft supported by a silicone tracheal prosthesis (in the surgery arm).
|
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有源比较器:Conventional treatment
radioactive iodine treatment +/- external beam radiotherapy +/- tyrosine kinase inhibitor, based on multidisciplinary team (MDT) decisions
|
radiotherapy and/or medical treatment
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
SAFETY / TOLERABILITY / EFFICACY
大体时间:Throughout the follow-up period of a minimum of 12 months and a maximum of 36 months.
|
local recurrence-free survival
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Throughout the follow-up period of a minimum of 12 months and a maximum of 36 months.
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
SAFETY / TOLERABILITY / EFFICACY
大体时间:During minimum 12 months and maximum 36 months.
|
- Overall mortality during the follow-up period (minimum 12 months, maximum 36 months).
|
During minimum 12 months and maximum 36 months.
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SAFETY / TOLERABILITY / EFFICACY
大体时间:minimum 12 months and maximum 36 months
|
Rates of in-hospital and late postoperative complications during the follow-up period (minimum 12 months, maximum 36 months).
|
minimum 12 months and maximum 36 months
|
|
SAFETY / TOLERABILITY / EFFICACY
大体时间:Before treatment initiation, and at 6 and 12 months
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Quality of life assessed using the St George's questionnaire (before treatment initiation, and at 6 and 12 months).
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Before treatment initiation, and at 6 and 12 months
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SAFETY / TOLERABILITY / EFFICACY
大体时间:POST-OPERATIVE (from M0 to M1)
|
R0 resection status (assessed postoperatively based on the pathological findings of the resected specimen) will be evaluated for patients in the surgical arm.
|
POST-OPERATIVE (from M0 to M1)
|
合作者和调查者
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
关键字
其他研究编号
- APHP200131
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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