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

Squamous Cell Carcinoma of the Oral Cavity Clinical Trial

— DIREKHT2  

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06030440
• Other study ID #: DIREKHT2
• Status: Recruiting
• Phase: Phase 2/Phase 3
• Start date: January 26, 2024
• Est. completion date: September 2033

Study information

• Verified date: August 2023
• Source: University of Erlangen-Nürnberg Medical School
• Contact: Marlen Haderlein, PD
• Phone: +49913185
• Email: marlen.haderlein[@]uk-erlangen.de
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 508
• Est. completion date: September 2033
• Est. primary completion date: December 2031
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Histologically proven squamous cell carcinoma of the oral cavity/larynx/oro-or hypopharynx (except glottis cancer (pT1/2pN0))

2. Surgery of primary tumor and neck dissection performed according to predefined surgical standard

3. Indication for postoperative radio(chemo)therapy

4. No lymph node metastases > 6cm

5. Lymph node metastases in not more than 3 lymph node level

6. No distant metastases (cM0)

7. Age = 18 years, no upper age limit

8. Eastern Cooperative Oncology Group (ECOG) = 2

9. Patients who understood protocol contents and are able to behave according to protocol

10. Signed study-specific consent form prior to therapy

11. 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:

1. macroscopic incomplete resection R2

2. Distant metastases (cM1)

3. Radiologically or histologically proven early recurrence after surgery (time frame from surgery to start of radio(chemo)therapy)

4. Lymph node metastases in > 3 lymph node level

5. pregnant or lactating/nursing women

6. fertile patients that are not willing to use highly effective methods of contraception (per institutional standards) during treatment

7. Any condition potentially hampering compliance with the study protocol and follow-up schedule

8. On-treatment participation on other clinical therapeutic trials

9. Prior tumor-specific therapy any other than surgery (like prior radiotherapy in the head and neck region, prior chemo- or immunotherapy (neoadjuvant/induction))

10. Patients who have contraindication for MRI and CT with contrast agent (both)

11. Prior (> 2 months before beginning of radio(chemo)therapy) neck dissection or surgery in the head and neck area affecting lymph drainage

12. 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

Related Conditions & MeSH terms

• Carcinoma
• Carcinoma, Squamous Cell
• Squamous Cell Carcinoma of Head and Neck
• Squamous Cell Carcinoma of the Hypopharynx
• Squamous Cell Carcinoma of the Larynx
• Squamous Cell Carcinoma of the Oral Cavity
• Squamous Cell Carcinoma of the Oropharynx

Intervention

Radiation:
• Eliminating RT to the elective neck
Reduction of radiation volume by eliminating radiotherapy to the elective neck
• RT standard of care
postoperative radiotherapy of the head and neck region according to current standard including elective nodal irradiation

Locations

Country	Name	City	State
Germany	Universitätsklinikum Erlangen, Strahlenklinik	Erlangen	Bavaria

Sponsors (1)

Lead Sponsor	Collaborator
University of Erlangen-Nürnberg Medical School

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Phase II: 1-year PEG feeding tube dependence rate	observe change of PEG-dependence due to different target volumes	PEG-dependent 1 year after radiotherapy
Primary	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)	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	Disease-free survival	Disease-free survival	up to 26 months
Secondary	Distant-metastasis-free survival	Distant-metastasis-free survival	through study completion, an average of 26 months
Secondary	Overall survival (OS)	Overall survival (OS)	up to 26 months
Secondary	Cause of death (tumor-related, not tumor-related)	Cause of death (tumor-related, not tumor-related)	through study completion, an average of 26 months
Secondary	Acute toxicity according to Common Terminology Criteria (CTC) version 5.0	Acute toxicity according to CTC version 5.0	up to 2 months
Secondary	Late toxicity according to CTC version 5.0	Late toxicity according to CTC version 5.0	up to 24 months