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Differentiated Thyroid CancerPhase 2TRITON 02NCT07823686

Tracheal Replacement Using A Cryopreserved Aortic Allograft For R0 Resection In Locally Advanced Thyroid Cancer (TRITON 02 Tracheal Replacement In ThyrOid caNcer)

A Phase 2 study testing Tracheal replacement using a cryopreserved aortic allograft for R0 resection in locally advanced thyroid cancer and Conventional treatment in people with Differentiated Thyroid Cancer, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Differentiated Thyroid Cancer
What is being tested?
Tracheal replacement using a cryopreserved aortic allograft for R0 resection in locally advanced thyroid cancer and Conventional treatment
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
1 siteFrance
Study dates
27 Jul 2027to 27 Aug 2030
Phase
Phase 2
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

  • 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;
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  • 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Christophe TRESSALLET, Pr contact

+33148955231

France1 site
  • Hôpital Avicenne

    Bobigny, Île-de-France Region, 93009 Bobigny Cedex

Other trials in France

About this study

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.

Read the detailed description

The main objective of the study is to compare the use of this innovative approach (tracheal replacement with stented cryopreserved aortic allograft) with standard therapy (local therapy, irradiation) in patients with extended thyroid cancer invading the trachea. Secondary objectives are to analyze R0 resection, postoperative mortality and morbidity rates, postoperative complications and quality of life.

Being tested
Tracheal replacement using a cryopreserved aortic allograft for R0 resection in locally advanced thyroid cancer, Conventional treatment
Keywords
differentiated thyroid cancer, Tracheal replacement, aortic allograft supported by a silicone stent, cryopreserved aortic allograft

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Tracheal replacement using a cryopreserved aortic allograft for R0 resection in locally advanced thyroid cancerProcedure or surgery

    Resection and replacement of the invaded tracheal segment with a cryopreserved aortic allograft supported by a silicone tracheal prosthesis (in the surgery arm).

  • Conventional treatmentOther

    radiotherapy and/or medical treatment

Study groups in NCT07823686
Study groupRoleWhat they receive
SurgeryExperimentalSurgical resection using the innovative approach
Receives: Procedure: Tracheal replacement using a cryopreserved aortic allograft for R0 resection in locally advanced thyroid cancer
Conventional treatmentActive comparatorradioactive iodine treatment +/- external beam radiotherapy +/- tyrosine kinase inhibitor, based on multidisciplinary team (MDT) decisions
Receives: Other: Conventional treatment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. SAFETY / TOLERABILITY / EFFICACY

    local recurrence-free survival

    Measured: Throughout the follow-up period of a minimum of 12 months and a maximum of 36 months.

Secondary outcomes (4)
  1. SAFETY / TOLERABILITY / EFFICACY

    • Overall mortality during the follow-up period (minimum 12 months, maximum 36 months).

    Measured: During minimum 12 months and maximum 36 months.

  2. SAFETY / TOLERABILITY / EFFICACY

    Rates of in-hospital and late postoperative complications during the follow-up period (minimum 12 months, maximum 36 months).

    Measured: minimum 12 months and maximum 36 months

  3. SAFETY / TOLERABILITY / EFFICACY

    Quality of life assessed using the St George's questionnaire (before treatment initiation, and at 6 and 12 months).

    Measured: Before treatment initiation, and at 6 and 12 months

  4. SAFETY / TOLERABILITY / EFFICACY

    R0 resection status (assessed postoperatively based on the pathological findings of the resected specimen) will be evaluated for patients in the surgical arm.

    Measured: POST-OPERATIVE (from M0 to M1)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Sep 2026
  2. Study start27 Jul 2027 (estimated)
  3. Primary completion27 Aug 2030 (estimated)
  4. Study completion27 Aug 2030 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Two parallel groups: Group 1: surgical group involving resection and replacement of the invaded tracheal segment with a cryopreserved aortic allograft supported by a silicone tracheal prosthesis; Group 2 : conventional treatment group (radiotherapy and/or medical treatment) recommended during a multidisciplinary team meeting.
Masking
None (open label)
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07823686
Sponsor's protocol ID
APHP200131
Acronym
TRITON 02
Status last verified
Sep 2026
First submitted
3 Sep 2026
Last updated
16 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Martinod E, Chouahnia K, Radu DM, Joudiou P, Uzunhan Y, Bensidhoum M, Santos Portela AM, Guiraudet P, Peretti M, Destable MD, Solis A, Benachi S, Fialaire-Legendre A, Rouard H, Collon T, Piquet J, Leroy S, Venissac N, Santini J, Tresallet C, Dutau H, Sebbane G, Cohen Y, Beloucif S, d'Audiffret AC, Petite H, Valeyre D, Carpentier A, Vicaut E. Feasibility of Bioengineered Tracheal and Bronchial Reconstruction Using Stented Aortic Matrices. JAMA. 2018 Jun 5;319(21):2212-2222. doi: 10.1001/jama.2018.4653.

    PubMed 29800033

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Tracheal replacement using a cryopreserved aortic allograft for R0 resection in locally advanced thyroid cancer and Conventional treatment in people with Differentiated Thyroid Cancer, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 16 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Emmanuel MARTINOD, Pr (+33148955231, +33689785327, emmanuel.martinod@aphp.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

SAFETY / TOLERABILITY / EFFICACY (time frame: Throughout the follow-up period of a minimum of 12 months and a maximum of 36 months.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07823686, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Sep 2026; AzTrials last refreshed its copy on 30 Oct 2026.

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