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Evaluation of the Efficacy and Safety of Local Cryotherapy Treatment of Recurrent Head and Neck Cancer in Irradiated Areas: a Pilot Study (CRYORL)

Primary Purpose

Recurrent Head and Neck Cancer, Local Cryotherapy Treatment

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
local cryotherapy treatment
Sponsored by
University Hospital, Strasbourg, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Recurrent Head and Neck Cancer

Eligibility Criteria

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

Inclusion Criteria: Malignant head/neck tumor Unresectable locoregional recurrence in a previously irradiated area Contraindication to re-irradiation Age > 18 years Performance index ≤ 2 (WHO) Life expectancy > 12 weeks Absence of hemostasis disorders Renal function: creatinine clearance ≥ 30 mL/min by CKD-EPI method (Cockcroft-Gault formula or MDRD) Subject affiliated to a social security health insurance plan Subject able to understand the objectives and risks of the research and to give dated and signed informed consent For a woman of childbearing age, negative blood pregnancy test at the inclusion visit Exclusion Criteria: Stage IV with distant metastases or multiple tumors Melanoma, sarcoma, and lymphoma Participants who have received chemotherapy or radiation therapy within 4 weeks Other active cancer within the past 2 years (patients with carcinoma in situ, papillary thyroid carcinoma, basal cell skin carcinoma, localized Gleason 6 prostate cancer, or breast cancer in situ are allowed) Concomitant therapy with any other systemic anticancer treatment Contraindication of anaesthesiology character Contraindication to MRI Participation in another clinical study Any social, medical or psychological condition that may prevent the patient from complying with the constraints of the protocol Any significant pathology that may interfere with the patient's participation in the study Subject under court protection Subject under guardianship or curatorship Pregnant or breastfeeding women

Sites / Locations

  • Hôpitaux Universitaires de Strasbourg

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

local cryotherapy treatment

Arm Description

Outcomes

Primary Outcome Measures

Local tumour control rate
Tumour control is defined as no increase in size and no suspicious contrast (or radiotracer) in the ablation area. Any suspected recurrence on cross-sectional imaging will be confirmed by biopsy.

Secondary Outcome Measures

Local tumour control rate
Tumour control is defined as no increase in size and no suspicious contrast (or radiotracer) in the ablation area. Any suspected recurrence on cross-sectional imaging will be confirmed by biopsy.
Rate of complications/adverse events (including serious) possibly related to cryotherapy
assessed by the NCI-CTCAE severity scale version 5.0
To evaluate the quality of life of patients
Scale EORTC-QLQ-C30
To evaluate the quality of life of patients
Scale EORTC - QLQ - H&N35
To evaluate the quality of life of patients
Scale VHI 10
To evaluate the quality of life of patients
Scale MDADI_v1.0
To evaluate the quality of life of patients
Scale DHI

Full Information

First Posted
January 30, 2023
Last Updated
August 10, 2023
Sponsor
University Hospital, Strasbourg, France
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1. Study Identification

Unique Protocol Identification Number
NCT05738187
Brief Title
Evaluation of the Efficacy and Safety of Local Cryotherapy Treatment of Recurrent Head and Neck Cancer in Irradiated Areas: a Pilot Study
Acronym
CRYORL
Official Title
Evaluation of the Efficacy and Safety of Local Cryotherapy Treatment of Recurrent Head and Neck Cancer in Irradiated Areas: a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 30, 2023 (Anticipated)
Primary Completion Date
October 30, 2025 (Anticipated)
Study Completion Date
November 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Strasbourg, France

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
In France, squamous cell carcinomas of the head and neck (SCCHN) are the 5th most common cancer. 60% of patients present with locally advanced tumors (stage III/IV), characterized by a poor prognosis (5-year survival not exceeding 60%). The standard treatment consists of either surgical removal followed by adjuvant radiochemotherapy or exclusive radiochemotherapy. In case of locoregional recurrence (about 40% of patients), salvage surgery can be proposed, allowing prolonged survival for less than one third of eligible patients. However, more than half of locoregional recurrences are unresectable. The standard treatment then consists of immunotherapy and/or chemotherapy for palliative purposes with a median survival of no more than 15 months. Stereotactic radiotherapy is another potentially curative option that allows a local control of 30-60% at 1 year, but at the cost of significant toxicity (up to 50% of grade 3-4 toxicities), thus limiting its indication. The issue of salvage treatment also applies to other rarer histological forms, including naso-sinus and salivary gland tumors, for which the probability of overall survival at 5 years does not exceed 65% due to locoregional evolution, despite advances in surgical techniques and the addition of radiotherapy. During the last two decades, minimally invasive interventional radiology techniques have been developed in the field of oncology. Among these techniques, cryotherapy is now commonly used for the treatment of several cancers. The multiplication of its indications is based on numerous clinical advantages (good post-operative analgesia, good toxicity profile, good tumor control). Cryotherapy could thus be a therapeutic alternative in head and neck cancers in recurrence situation in irradiated and unresectable territory, allowing to maintain a curative project in a higher proportion of patients and also to have a more favorable toxicity profile than re-irradiation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Head and Neck Cancer, Local Cryotherapy Treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
local cryotherapy treatment
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
local cryotherapy treatment
Intervention Description
cryotherapy
Primary Outcome Measure Information:
Title
Local tumour control rate
Description
Tumour control is defined as no increase in size and no suspicious contrast (or radiotracer) in the ablation area. Any suspected recurrence on cross-sectional imaging will be confirmed by biopsy.
Time Frame
at 12 months
Secondary Outcome Measure Information:
Title
Local tumour control rate
Description
Tumour control is defined as no increase in size and no suspicious contrast (or radiotracer) in the ablation area. Any suspected recurrence on cross-sectional imaging will be confirmed by biopsy.
Time Frame
at 6 months post-procedure
Title
Rate of complications/adverse events (including serious) possibly related to cryotherapy
Description
assessed by the NCI-CTCAE severity scale version 5.0
Time Frame
at 12 months
Title
To evaluate the quality of life of patients
Description
Scale EORTC-QLQ-C30
Time Frame
at 1, 3, 6 and 12 months after cryotherapy
Title
To evaluate the quality of life of patients
Description
Scale EORTC - QLQ - H&N35
Time Frame
at 1, 3, 6 and 12 months after cryotherapy
Title
To evaluate the quality of life of patients
Description
Scale VHI 10
Time Frame
at 1, 3, 6 and 12 months after cryotherapy
Title
To evaluate the quality of life of patients
Description
Scale MDADI_v1.0
Time Frame
at 1, 3, 6 and 12 months after cryotherapy
Title
To evaluate the quality of life of patients
Description
Scale DHI
Time Frame
at 1, 3, 6 and 12 months after cryotherapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Malignant head/neck tumor Unresectable locoregional recurrence in a previously irradiated area Contraindication to re-irradiation Age > 18 years Performance index ≤ 2 (WHO) Life expectancy > 12 weeks Absence of hemostasis disorders Renal function: creatinine clearance ≥ 30 mL/min by CKD-EPI method (Cockcroft-Gault formula or MDRD) Subject affiliated to a social security health insurance plan Subject able to understand the objectives and risks of the research and to give dated and signed informed consent For a woman of childbearing age, negative blood pregnancy test at the inclusion visit Exclusion Criteria: Stage IV with distant metastases or multiple tumors Melanoma, sarcoma, and lymphoma Participants who have received chemotherapy or radiation therapy within 4 weeks Other active cancer within the past 2 years (patients with carcinoma in situ, papillary thyroid carcinoma, basal cell skin carcinoma, localized Gleason 6 prostate cancer, or breast cancer in situ are allowed) Concomitant therapy with any other systemic anticancer treatment Contraindication of anaesthesiology character Contraindication to MRI Participation in another clinical study Any social, medical or psychological condition that may prevent the patient from complying with the constraints of the protocol Any significant pathology that may interfere with the patient's participation in the study Subject under court protection Subject under guardianship or curatorship Pregnant or breastfeeding women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Luigi Roberto CAZZATO, MD
Phone
03 69 55 16 35
Ext
0033
Email
roberto-luigi.cazzato@chru-strasbourg.fr
Facility Information:
Facility Name
Hôpitaux Universitaires de Strasbourg
City
Strasbourg
ZIP/Postal Code
67000
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luigi Roberto CAZZATO, MD
Phone
03 69 55 16 35
Ext
0033
Email
robertoluigi.cazzato@chru-strasbourg.fr

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Evaluation of the Efficacy and Safety of Local Cryotherapy Treatment of Recurrent Head and Neck Cancer in Irradiated Areas: a Pilot Study

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