IORT in Local Advanced Laryngocarcinoma (ILAL)
Primary Purpose
Laryngeal Neoplasms
Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
IORT
surgery
External radiotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Laryngeal Neoplasms
Eligibility Criteria
Inclusion Criteria:
- adults over the age of 18;
- radiographic or pathological diagnosis of local advanced laryngocarcinoma (according to NCCN guidelines);
- the expected survival time ≥ 3 months;
- sign informed consent for treatment and research with self-knowledge.
Exclusion Criteria:
- there is distant metastasis;
- pregnant women;
- patients with CT/MRI contraindications;
- the patient fails to receive treatment and/or follow-up as scheduled;
- bad fluid and organ function decompensation;
- multiple primary cancers;
- patients participating in other trials.
Sites / Locations
- Tianjin First Central HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
with IORT
without IORT
Arm Description
Outcomes
Primary Outcome Measures
2-year local recurrence rate
In this study, no matter whether distant metastases occurred, if there was the presence of any anastomotic or lateral node recurrences, it was defined as local recurrence.
Criteria for local recurrence include (1) MRI results suggests local tumor recurrence, (2)Laryngoscopy indicates local tumor recurrence.
Secondary Outcome Measures
2-year disease free survival
Compare 2-year disease free survival in patients with local advanced laryngocarcinoma treated with or without IORT.
Criteria for disease free survival means MRI and laryngoscopy (PET-CT if possible) indicate tumor free.
2-year overall survival
Compare 2-year overall survival in patients with local advanced laryngocarcinoma treated with or without IORT.
tissue necrosis
Compare the risk of tissue necrosis as determined visually by the Laryngoscope at 2 years after treatment in patients with local advanced laryngocarcinoma treated with or without IORT.
fibrosis
Compare the risk of fibrosis as determined visually by the Laryngoscope at 2 years after treatment in patients with local advanced laryngocarcinoma treated with or without IORT.
time of wound healing
Compare the time of wound healing after surgery in patients with local advanced laryngocarcinoma treated with or without IORT.
Full Information
NCT ID
NCT04278638
First Posted
January 16, 2020
Last Updated
October 21, 2020
Sponsor
Tianjin First Central Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04278638
Brief Title
IORT in Local Advanced Laryngocarcinoma
Acronym
ILAL
Official Title
Study of Safety and Feasibility With or Without Intraoperative Radiation in Local Advanced Laryngocarcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
July 1, 2022 (Anticipated)
Study Completion Date
December 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tianjin First Central Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The incidence of laryngeal cancer accounts for about 1 ~ 5% of the total body tumors. For the surgical treatment of laryngeal cancer, the development trend of laryngocarcinoma treatment is to improve the local control rate, preserve the laryngeal function of patients as far as possible, and improve the life quality of patients. The efficacy, safety and feasibility of intraoperative radiotherapy (IORT) in head and neck cancer has been demonstrated in multiple institutional (3-5) studies to optimize local control. It is still unclear whether IORT can improve the local control and have efficacy, safety and feasibility in clinic. The purpose of this study was to observe the efficacy, safety and feasibility of IORT in local advanced laryngocarcinoma .
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Laryngeal Neoplasms
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
with IORT
Arm Type
Experimental
Arm Title
without IORT
Arm Type
Active Comparator
Intervention Type
Radiation
Intervention Name(s)
IORT
Intervention Description
IORT in surgery of laryngocarcinoma
Intervention Type
Procedure
Intervention Name(s)
surgery
Intervention Description
total laryngectomy or hemilaryngectomy
Intervention Type
Radiation
Intervention Name(s)
External radiotherapy
Intervention Description
External radiotherapy
Primary Outcome Measure Information:
Title
2-year local recurrence rate
Description
In this study, no matter whether distant metastases occurred, if there was the presence of any anastomotic or lateral node recurrences, it was defined as local recurrence.
Criteria for local recurrence include (1) MRI results suggests local tumor recurrence, (2)Laryngoscopy indicates local tumor recurrence.
Time Frame
2 year
Secondary Outcome Measure Information:
Title
2-year disease free survival
Description
Compare 2-year disease free survival in patients with local advanced laryngocarcinoma treated with or without IORT.
Criteria for disease free survival means MRI and laryngoscopy (PET-CT if possible) indicate tumor free.
Time Frame
2 years
Title
2-year overall survival
Description
Compare 2-year overall survival in patients with local advanced laryngocarcinoma treated with or without IORT.
Time Frame
2 years
Title
tissue necrosis
Description
Compare the risk of tissue necrosis as determined visually by the Laryngoscope at 2 years after treatment in patients with local advanced laryngocarcinoma treated with or without IORT.
Time Frame
2 years
Title
fibrosis
Description
Compare the risk of fibrosis as determined visually by the Laryngoscope at 2 years after treatment in patients with local advanced laryngocarcinoma treated with or without IORT.
Time Frame
2 years
Title
time of wound healing
Description
Compare the time of wound healing after surgery in patients with local advanced laryngocarcinoma treated with or without IORT.
Time Frame
up to 1 month
Other Pre-specified Outcome Measures:
Title
pharyngeal fistula
Description
Pharyngeal fistula means that saliva is stored in subcutaneous or subincisional tissues, resulting in abscess cavity rupture to the skin or incision margin, making the hypopharyngeal and esophageal lumen communicate with the skin to form a sinus tract, through which saliva or food can spill out to the skin, forming a skin fistula.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
adults over the age of 18;
radiographic or pathological diagnosis of local advanced laryngocarcinoma (according to NCCN guidelines);
the expected survival time ≥ 3 months;
sign informed consent for treatment and research with self-knowledge.
Exclusion Criteria:
there is distant metastasis;
pregnant women;
patients with CT/MRI contraindications;
the patient fails to receive treatment and/or follow-up as scheduled;
bad fluid and organ function decompensation;
multiple primary cancers;
patients participating in other trials.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xinyuan Gong
Phone
+8613436640313
Email
gxy0007@163.com
Facility Information:
Facility Name
Tianjin First Central Hospital
City
Tianjin
State/Province
Tianjin
ZIP/Postal Code
300000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xinyuan Gong
Phone
+8613436640313
Email
gxy0007@163.com
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
32762662
Citation
Yang Y, Li L, Zheng Y, Liu Q, Wei X, Gong X, Wang W, Lin P. A prospective, single-arm, phase II clinical trial of intraoperative radiotherapy using a low-energy X-ray source for local advanced Laryngocarcinoma (ILAL): a study protocol. BMC Cancer. 2020 Aug 6;20(1):734. doi: 10.1186/s12885-020-07233-1.
Results Reference
derived
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IORT in Local Advanced Laryngocarcinoma
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