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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05057143
Other study ID # CWP-2021-7-3
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 10, 2022
Est. completion date December 2025

Study information

Verified date March 2024
Source Blokhin's Russian Cancer Research Center
Contact Alexander Salkov
Phone +79629346738
Email salkov1994@icloud.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A patient with a tumor lesion of the chest wall undergoes CT scan with a step width of less than 1 mm, then engineers design an individual model to replace the defect. Using a 3D printer, a model is made based on titanium alloy powder. Preoperative preparation takes an average of 14-21 days. The next stage is surgical treatment in the amount of resection of the chest wall with plastic defect with an individual titanium implant. In some cases, the titanium framework is separated from the pleural cavity by a polytetrafluoroethylene plate in order to seal and prevent the development of pulmonary hernias. The advantages of titanium individual prostheses include accurate matching of the implant to the size and characteristics of the defect, individual modeling allows you to repeat the anatomical features of the patient. This method helps to recreate the original shape of the chest, and most importantly, symmetrical, relatively healthy half. With the help of titanium, individualized prostheses are made based on 3D modeling, which will reduce the incidence of complications, accelerate rehabilitation and improve the quality of life of patients with tumor lesions of the chest wall. The postoperative period takes 15-30 days.


Description:

A patient with a tumor lesion of the chest wall undergoes CT scan with a step width of less than 1 mm, then engineers design an individual model to replace the defect. Using a 3D printer, a model is made based on the patient's anthropometric data. Manufacturing takes place by 3D printing on a titanium alloy powder certified for the manufacture of medical implants. The technology used is a type of SLS (Selective Laser Sintering) -technology, layer-by-layer laser melting of metal-powder compositions. The printing process begins with dividing the digital 3D model of the product into layers with a thickness of 20 to 100 microns in order to create a 2D image of each layer of the product (section). The industry standard format is STL (Stereolithography) file. This file enters a special machine software, where the information is analyzed and compared with the technical capabilities of the machine. Based on the data obtained, a production cycle of construction is launched, consisting of many cycles of building individual layers of the product. The cycle for constructing a layer (section) consists of typical operations: - applying a layer of powder of a given thickness to the construction plate; - scanning by a laser beam of the section of the product layer. The laser beam is a source of heat, under the influence of which the particles of the material are sintered along the profile of the section of the model; - lowering the platform into the depth of the construction well by an amount corresponding to the thickness of the construction layer. The process of building products takes place in the SLM (Selective Laser Melting) chamber of the machine, filled with an inert gas argon. After construction, the product is removed from the printer chamber and sent for heat treatment, annealing, to relieve internal stresses and improve mechanical properties. After annealing, the product is separated from the platform and undergoes finishing, which combines various types of machining. The final stages of the technological process are product cleaning and technical quality control. Preoperative preparation takes an average of 14-21 days. The next stage is surgical treatment in the amount of resection of the chest wall with plastic defect with an individual titanium implant. In all cases, the titanium framework is separated from the pleural cavity by a synthetic polyester (Dacron) plate in order to seal and prevent the development of pulmonary hernias. The advantages of titanium individual implants include accurate matching of the implant to the size and characteristics of the defect, individual modeling allows you to repeat the anatomical features of the patient. This method helps to recreate the original shape of the chest, and most importantly, symmetrical, relatively healthy half. With the help of titanium, individualized prostheses are made based on 3D modeling, which will reduce the incidence of complications, accelerate rehabilitation and improve the quality of life of patients with tumor lesions of the chest wall. The postoperative period takes 15-30 days.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 2025
Est. primary completion date December 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Malignant neoplasm of ribs, sternum and clavicle - Malignant neoplasm of the connective and soft tissues of the chest - Neoplasm of uncertain or unknown nature of ribs, sternum and collarbone - Benign neoplasm of ribs, sternum and collarbone - Tumor lesions of the chest wall of any localization, malignant and benign, as well as of an uncertain or unknown nature - For malignant tumors: Grade 1-3 - Lack of distant metastases - Signed informed consent Exclusion Criteria: - Children, women during pregnancy, childbirth, women during breastfeeding. - Military personnel, with the exception of contract military personnel. - Persons with mental disorders. - Persons detained, taken into custody, serving a sentence in the form of restriction of freedom, arrest, imprisonment or administrative arrest. - Patients with distant metastases (except for a solitary focus in the chest wall without other manifestations of the disease) - Inoperable tumor - The presence of another malignant tumor at the time of examination - ECOG 4 - Having an active or chronic fungal / bacterial / viral infection - Uncontrolled chronic diseases of the liver, kidneys in the acute stage - Presence of metastases

Study Design


Intervention

Device:
Implants
3D printed implants
Plates
Titanium plates

Locations

Country Name City State
Russian Federation Federal State Budgetary Institution "N.N. Blokhin National Medical Research Center of Oncology" ?f the Ministry of Health of the Russian Federation Moscow

Sponsors (1)

Lead Sponsor Collaborator
Blokhin's Russian Cancer Research Center

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary Disease-free survival Time after treatment during which no sign of cancer is found 24 months
Secondary Comparison of hospitalization rate Time after surgery till the end of hospitalization 30 days
Secondary Comparison of safety assessment Adverse Event Assessment and Serious Adverse Event Assessment according to CTCAE 5.0 24 months
Secondary Comparison of performance status according Karnofsky scale Improvement on the Karnofsky scale by 10-30 points 24 months
Secondary Comparison of pain relief according Visual Analogue Scale Improvement on the Visual Analogue Scale by 3-5 points 24 months
Secondary Comparison of pain relief according Whatkins scale Improvement on the Whatkins scale by 1-2 points 24 months
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