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De-Intensification of Postoperative Radiotherapy in Patients With Squamous Cell Carcinoma of the Head and Neck (DIREKHT2)

Primary Purpose

Squamous Cell Carcinoma of the Oral Cavity, Squamous Cell Carcinoma of the Larynx, Squamous Cell Carcinoma of the Hypopharynx

Status
Not yet recruiting
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
Eliminating RT to the elective neck
RT standard of care
Sponsored by
University of Erlangen-Nürnberg Medical School
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Squamous Cell Carcinoma of the Oral Cavity

Eligibility Criteria

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

Inclusion Criteria: Histologically proven squamous cell carcinoma of the oral cavity/larynx/oro-or hypopharynx (except glottis cancer (pT1/2pN0)) Surgery of primary tumor and neck dissection performed according to predefined surgical standard Indication for postoperative radio(chemo)therapy No lymph node metastases > 6cm Lymph node metastases in not more than 3 lymph node level No distant metastases (cM0) Age ≥ 18 years, no upper age limit Eastern Cooperative Oncology Group (ECOG) ≤ 2 Patients who understood protocol contents and are able to behave according to protocol Signed study-specific consent form prior to therapy Start of radiotherapy at least 6 weeks after last tumor-specific surgery (e.g. resection primary tumor, neck dissection, excluded are surgeries according to wound healing complications) Exclusion Criteria: macroscopic incomplete resection R2 Distant metastases (cM1) Radiologically or histologically proven early recurrence after surgery (time frame from surgery to start of radio(chemo)therapy) Lymph node metastases in > 3 lymph node level pregnant or lactating/nursing women fertile patients that are not willing to use highly effective methods of contraception (per institutional standards) during treatment Any condition potentially hampering compliance with the study protocol and follow-up schedule On-treatment participation on other clinical therapeutic trials Prior tumor-specific therapy any other than surgery (like prior radiotherapy in the head and neck region, prior chemo- or immunotherapy (neoadjuvant/induction)) Patients who have contraindication for MRI and CT with contrast agent (both) Prior (> 2 months before beginning of radio(chemo)therapy) neck dissection or surgery in the head and neck area affecting lymph drainage History of another primary malignancy except for malignancy treated with curative intent and with no known active disease ≥5 years before diagnosis of head and neck cancer, adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease, adequately treated carcinoma in situ without evidence of disease

Sites / Locations

  • Universitätsklinikum Erlangen, Strahlenklinik

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Control Arm

Investigational Arm

Arm Description

postoperative radiotherapy of the head and neck region according to current standard including elective nodal irradiation

postoperative radiotherapy of the head and neck region without elective nodal irradiation

Outcomes

Primary Outcome Measures

Phase II: 1-year PEG feeding tube dependence rate
observe change of PEG-dependence due to different target volumes
Phase III: Time to local relapse
difference between the date of randomization and the date of observation of local relapse (LR), or the date of last observation if no LR occurred (censored observation)

Secondary Outcome Measures

Disease-free survival
Disease-free survival
Distant-metastasis-free survival
Distant-metastasis-free survival
Overall survival (OS)
Overall survival (OS)
Cause of death (tumor-related, not tumor-related)
Cause of death (tumor-related, not tumor-related)
Acute toxicity according to Common Terminology Criteria (CTC) version 5.0
Acute toxicity according to CTC version 5.0
Late toxicity according to CTC version 5.0
Late toxicity according to CTC version 5.0

Full Information

First Posted
August 11, 2023
Last Updated
September 8, 2023
Sponsor
University of Erlangen-Nürnberg Medical School
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1. Study Identification

Unique Protocol Identification Number
NCT06030440
Brief Title
De-Intensification of Postoperative Radiotherapy in Patients With Squamous Cell Carcinoma of the Head and Neck
Acronym
DIREKHT2
Official Title
De-Intensification of Postoperative Radiotherapy in Patients With Squamous Cell Carcinoma of the Head and Neck
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 2023 (Anticipated)
Primary Completion Date
September 2031 (Anticipated)
Study Completion Date
September 2033 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Erlangen-Nürnberg Medical School

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This randomized, prospective, multicenter phase II/III trial will study the reduction of radiation volume by eliminating radiotherapy (RT) to the elective neck using strictly defined surgical and radio-oncological standards to reduce radiotherapy-related long-term side effects without affecting locoregional control.
Detailed Description
This study aims to determine whether it is possible to achieve an individual target volume concept that eliminates elective irradiation of uninvolved lymph drainage areas while maintaining clearly defined surgical standards and using modern imaging and radiation techniques. The aim of this study is to achieve reduced late toxicity without compromising locoregional control. Patients will be randomized to: either RT to primary tumor region, regions with lymph node metastases and elective nodal irradiation (control arm) or RT to primary tumor region and regions with lymph node metastases without elective nodal irradiation (investigational arm) A two-stage design was chosen for this purpose. Phase II: A randomized phase II study whose primary endpoint is the 1-year percutaneous endoscopic gastrostomy (PEG) tube dependence rate will be performed first. Phase III: If the primary endpoint of the phase II study is met and the interim analysis shows no increase in the locoregional recurrence rate in the study/investigational arm, the study will be continued as a phase III study whose primary endpoint is the locoregional control rate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Squamous Cell Carcinoma of the Oral Cavity, Squamous Cell Carcinoma of the Larynx, Squamous Cell Carcinoma of the Hypopharynx, Squamous Cell Carcinoma of the Oropharynx

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
508 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control Arm
Arm Type
Active Comparator
Arm Description
postoperative radiotherapy of the head and neck region according to current standard including elective nodal irradiation
Arm Title
Investigational Arm
Arm Type
Experimental
Arm Description
postoperative radiotherapy of the head and neck region without elective nodal irradiation
Intervention Type
Radiation
Intervention Name(s)
Eliminating RT to the elective neck
Intervention Description
Reduction of radiation volume by eliminating radiotherapy to the elective neck
Intervention Type
Radiation
Intervention Name(s)
RT standard of care
Intervention Description
postoperative radiotherapy of the head and neck region according to current standard including elective nodal irradiation
Primary Outcome Measure Information:
Title
Phase II: 1-year PEG feeding tube dependence rate
Description
observe change of PEG-dependence due to different target volumes
Time Frame
PEG-dependent 1 year after radiotherapy
Title
Phase III: Time to local relapse
Description
difference between the date of randomization and the date of observation of local relapse (LR), or the date of last observation if no LR occurred (censored observation)
Time Frame
From the date of randomization until the date of observation of local relapse or the date of last observation if no LR occurred, whichever came first (assessed up to 26 months)
Secondary Outcome Measure Information:
Title
Disease-free survival
Description
Disease-free survival
Time Frame
up to 26 months
Title
Distant-metastasis-free survival
Description
Distant-metastasis-free survival
Time Frame
through study completion, an average of 26 months
Title
Overall survival (OS)
Description
Overall survival (OS)
Time Frame
up to 26 months
Title
Cause of death (tumor-related, not tumor-related)
Description
Cause of death (tumor-related, not tumor-related)
Time Frame
through study completion, an average of 26 months
Title
Acute toxicity according to Common Terminology Criteria (CTC) version 5.0
Description
Acute toxicity according to CTC version 5.0
Time Frame
up to 2 months
Title
Late toxicity according to CTC version 5.0
Description
Late toxicity according to CTC version 5.0
Time Frame
up to 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically proven squamous cell carcinoma of the oral cavity/larynx/oro-or hypopharynx (except glottis cancer (pT1/2pN0)) Surgery of primary tumor and neck dissection performed according to predefined surgical standard Indication for postoperative radio(chemo)therapy No lymph node metastases > 6cm Lymph node metastases in not more than 3 lymph node level No distant metastases (cM0) Age ≥ 18 years, no upper age limit Eastern Cooperative Oncology Group (ECOG) ≤ 2 Patients who understood protocol contents and are able to behave according to protocol Signed study-specific consent form prior to therapy Start of radiotherapy at least 6 weeks after last tumor-specific surgery (e.g. resection primary tumor, neck dissection, excluded are surgeries according to wound healing complications) Exclusion Criteria: macroscopic incomplete resection R2 Distant metastases (cM1) Radiologically or histologically proven early recurrence after surgery (time frame from surgery to start of radio(chemo)therapy) Lymph node metastases in > 3 lymph node level pregnant or lactating/nursing women fertile patients that are not willing to use highly effective methods of contraception (per institutional standards) during treatment Any condition potentially hampering compliance with the study protocol and follow-up schedule On-treatment participation on other clinical therapeutic trials Prior tumor-specific therapy any other than surgery (like prior radiotherapy in the head and neck region, prior chemo- or immunotherapy (neoadjuvant/induction)) Patients who have contraindication for MRI and CT with contrast agent (both) Prior (> 2 months before beginning of radio(chemo)therapy) neck dissection or surgery in the head and neck area affecting lymph drainage History of another primary malignancy except for malignancy treated with curative intent and with no known active disease ≥5 years before diagnosis of head and neck cancer, adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease, adequately treated carcinoma in situ without evidence of disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marlen Haderlein, PD
Phone
+49913185
Ext
33968
Email
marlen.haderlein@uk-erlangen.de
First Name & Middle Initial & Last Name or Official Title & Degree
Studiensekretariat
Phone
+49913185
Ext
33968
Email
studiensekretariat.ST@uk-erlangen.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarina Müller, PD
Organizational Affiliation
Universitätsklinikum Erlangen, HNO
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Rainer Fietkau, Prof
Organizational Affiliation
Universitätsklinikum Erlangen, Radiation Oncology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universitätsklinikum Erlangen, Strahlenklinik
City
Erlangen
State/Province
Bavaria
ZIP/Postal Code
91054
Country
Germany
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marlen Haderlein, PD
Phone
+49913185
Ext
33968
Email
marlen.haderlein@uk-erlangen.de
First Name & Middle Initial & Last Name & Degree
Rainer Fietkau, Prof
Phone
+49913185
Ext
33968
Email
rainer.fietkau@uk-erlangen.de

12. IPD Sharing Statement

Plan to Share IPD
No

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De-Intensification of Postoperative Radiotherapy in Patients With Squamous Cell Carcinoma of the Head and Neck

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