search
Back to results

Airway and/or Pulmonary Vessels Transplantation (TRACHBRONCAR)

Primary Purpose

Lung Cancer, Tracheal Neoplasm, Tracheal Stenosis

Status
Completed
Phase
Phase 1
Locations
France
Study Type
Interventional
Intervention
Airway and/or pulmonary Vessels Transplantation
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Lung Cancer focused on measuring Bronchial disease, Lung cancer surgery, Aorta/aortic Allograft, homograft, Tracheal disease, Benign, Malignant

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patient age ≥18 years and patient capable of giving consent to the carrying out of a medical research procedure
  • patient with proximal Lung Cancer (LC) requiring surgical resection (carinal resection, pneumonectomy, bronchoplastic lobectomy) after neoadjuvant chemotherapy or not and with adequate preoperative lung function tests
  • or patient with proximal LC requiring a pneumonectomy without adequate preoperative lung function tests
  • patients with extended lesions malignant or benign of the trachea without bronchitic lesion and who are in therapeutic impasse.
  • or patient older than 70 years with proximal LC requiring a pneumonectomy
  • decision made by a multidisciplinary team
  • patient information and consent

Exclusion Criteria:

  • patient age < 18 years or patient not capable of giving consent to the carrying out of a medical research procedure
  • patient with proximal or peripheral LC requiring a simple lobectomy
  • patient with unresectable LC because of major local involvement, N3 and/or M1 status(with the exception of a unique resectable brain metastasis)
  • patient with tracheal lesion that can be isolated from a simple resection anastomosis tracheal
  • iodine allergy
  • preoperative evaluation not allowing a simple lobectomy
  • patient not affiliated to the French Social Security System

Sites / Locations

  • Assistance Publique Hôpitaux de Paris, Hôpital Avicenne, CHU Paris-Seine-Saint-Denis

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

single arm surgery

Arm Description

Airway and/or pulmonary Vessels Transplantation

Outcomes

Primary Outcome Measures

90-day mortality

Secondary Outcome Measures

90-day morbidity

Full Information

First Posted
April 7, 2011
Last Updated
September 7, 2020
Sponsor
Assistance Publique - Hôpitaux de Paris
search

1. Study Identification

Unique Protocol Identification Number
NCT01331863
Brief Title
Airway and/or Pulmonary Vessels Transplantation
Acronym
TRACHBRONCAR
Official Title
Replacement of the Airways and/or the Pulmonary Vessels Using a Cryopreserved Arterial Allograft
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
May 31, 2011 (Actual)
Primary Completion Date
August 31, 2018 (Actual)
Study Completion Date
November 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
First study (BRONC-ART) The purpose of this prospective study is to evaluate the 90-day morbidity and mortality rates of bronchial transplantation using cryopreserved aortic allograft in proximal lung cancer surgery. The investigators hypothesize that this stage 1-2 surgical innovation could be safe and effective in order to reduce the 90-day morbidity and mortality rates compared to those observed with pneumonectomy, especially when some factors are present: age > 70 years, right side, neoadjuvant chemoradiotherapy. Current study (TRACHEO BRONC-ART) The BRONC-ART study was extended to major (malignant or benign) lesions of the trachea requiring airway transplantation. For these patients, resection followed by direct end to end anastomosis is not possible or at high risk.
Detailed Description
Surgery remains the best option for curative treatment of early stages Non-Small Cell Lung Cancer (NSCLC). Peripheral tumors are usually resected using lobectomy with a low 90-day morbidity and mortality rate (2%). Central NSCLC often require a pneumonectomy with a high 90-day morbidity and mortality rate (up to 24%), especially when some factors are present: age > 70 years, right side, neoadjuvant chemoradiotherapy. On the other hand, bronchoplastic lobectomies have been proposed in order to avoid pneumonectomy. However, more than fifty years after their first description, bronchoplastic lobectomies remain uncommon (<1% of all pulmonary resection). This could be explained by some technical difficulties showing the potential interest of a bronchial substitute. In a 10-year research phase on a sheep model (n=108), we demonstrated that aortic grafts could be valuable substitutes for tracheobronchial replacement. We observed a progressive transformation of the aortic tissue into airway tissue comprising epithelium and regenerated cartilage. The technique was extended to clinical tracheal replacement by us and others with encouraging results. We proposed to evaluate the feasibility of the use of a stent-supported cryopreserved aortic allograft as a bronchial substitute to prevent pneumonectomy and its associated high mortality rate in NSCLC surgery. Primary outcome will be the 90-day mortality. Secondary outcomes will be the postoperative complications, the 90-day morbidity. This prospective open study will include 20 to 30 patients according to eligibility criteria (see below). The operation will consist of the curative resection of the NSCLC followed by the replacement of a bronchial segment using a cryopreserved allograft in order to re-implant a functional pulmonary lobe. A stent will be placed in the graft to prevent airway collapse. -Current study (TRACHEO BRONC-ART) The BRONC-ART study was extended to major (malignant or benign) lesions of the trachea requiring airway transplantation. For these patients, resection followed by direct end to end anastomosis is not possible or at high risk.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer, Tracheal Neoplasm, Tracheal Stenosis
Keywords
Bronchial disease, Lung cancer surgery, Aorta/aortic Allograft, homograft, Tracheal disease, Benign, Malignant

7. Study Design

Primary Purpose
Other
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
single arm surgery
Arm Type
Experimental
Arm Description
Airway and/or pulmonary Vessels Transplantation
Intervention Type
Procedure
Intervention Name(s)
Airway and/or pulmonary Vessels Transplantation
Intervention Description
Use of a stent-supported aortic allograft to prevent pneumonectomy in lung cancer SURGERY
Primary Outcome Measure Information:
Title
90-day mortality
Time Frame
3 months
Secondary Outcome Measure Information:
Title
90-day morbidity
Time Frame
90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patient age ≥18 years and patient capable of giving consent to the carrying out of a medical research procedure patient with proximal Lung Cancer (LC) requiring surgical resection (carinal resection, pneumonectomy, bronchoplastic lobectomy) after neoadjuvant chemotherapy or not and with adequate preoperative lung function tests or patient with proximal LC requiring a pneumonectomy without adequate preoperative lung function tests patients with extended lesions malignant or benign of the trachea without bronchitic lesion and who are in therapeutic impasse. or patient older than 70 years with proximal LC requiring a pneumonectomy decision made by a multidisciplinary team patient information and consent Exclusion Criteria: patient age < 18 years or patient not capable of giving consent to the carrying out of a medical research procedure patient with proximal or peripheral LC requiring a simple lobectomy patient with unresectable LC because of major local involvement, N3 and/or M1 status(with the exception of a unique resectable brain metastasis) patient with tracheal lesion that can be isolated from a simple resection anastomosis tracheal iodine allergy preoperative evaluation not allowing a simple lobectomy patient not affiliated to the French Social Security System
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emmanuel MARTINOD, Pr, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Study Director
Facility Information:
Facility Name
Assistance Publique Hôpitaux de Paris, Hôpital Avicenne, CHU Paris-Seine-Saint-Denis
City
Bobigny
State/Province
Seine-Saint-Denis
ZIP/Postal Code
93000
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
29800033
Citation
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.
Results Reference
derived

Learn more about this trial

Airway and/or Pulmonary Vessels Transplantation

We'll reach out to this number within 24 hrs