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Head and Neck (HNSCC)NCT07801235

HYperfractionated Radiation Therapy Versus Concurrent Chemoradiation for Head and Neck Cancer (HYTC)

A study testing 70 gy 35 fractions/7weeks+high dose of cisplatin and 81.6 Gy /68 fractions BID FOR 7 WEEKS in people with Head and Neck (HNSCC), run by King Hussein Cancer Center at 1 site in Jordan.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This is an international multi-centre, non-inferiority phase III randomized controlled trial comparing concurrent chemoradiation with high dose cisplatin (Arm A) vs. hyperfractionated radiation therapy (Arm B) in patients with head and neck squamous cell carcinoma. Read more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Head and Neck (HNSCC)
What is being tested?
70 gy 35 fractions/7weeks+high dose of cisplatin and 81.6 Gy /68 fractions BID FOR 7 WEEKS
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
604 participants
Where
1 siteJordan
Study dates
20 Aug 2026to 1 Apr 2033
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Inclusion Criteria: Patients with pathologically (histologically or cytologically) proven diagnosis of HNSCC (larynx, hypopharynx, or oropharynx). Pathologic confirmation may be from either nodal or primary tumour. If a biopsy is obtained from nodal disease, a clinically apparent primary tumour on imaging and/or clinical examination must be present.

Diagnostic tonsillectomy or local excision of the primary without removal of nodal disease is permitted.

Diagnostic lymph node excision or limited neck dissections (retrieving ≤ 4 nodes) are permitted HPV positive or negative (by p16 immunohistochemistry). OPC will be classified as p16 at local sites based on greater than 70% strong diffuse nuclear or nuclear and cytoplasmic staining.

For patients with OPC: analysis of p16 status is required For patients with laryngeal/hypopharyngeal cancer: analysis of p16 status is NOT required

Clinical stage T1-2 N1-2 M0 or T3 N0-2 M0 (UICC/AJCC TNM 8th Edition). Staging will be determined based on clinical examination, axial imaging (CT and/or MRI), and whenever available, PET-CT imaging.

The following radiological investigations must be done within 8 weeks of registration:

CT or MRI of the head and neck; PET-CT scan or chest CT scan (PET-CT scan is strongly preferred and highly recommended to be used for eligibility).

Planned definitive RT. Based on clinical and laboratory evaluation and in keeping with local institutional standards, the treating oncologist must declare upfront, that in the absence of the present clinical trial, the patient would be candidate for treatment with concurrent high dose cisplatin every 3 weeks. This would include:

Adequate hematologic function must be documented within 8 weeks prior to registration:

Hemoglobin levels of > 8g/dL (the use of transfusion or other intervention to achieve hemoglobin ≥ 8 g/dL is acceptable) Platelet count of >100,000 cells/mm3. ANC of > 1500 cells/mm3.

Adequate hepatic function must be documented within 8 weeks prior to registration:

Total bilirubin < 2 X institutional upper limit of normal. AST (SGOT)/ALT (SGPT) ≤ 2.5 X institutional upper limit of normal. Albumin ≥ 3.0 g/dL.

Adequate renal function must be documented within 8 weeks prior to registration:

Serum creatinine < 1.5 mg/dl or creatinine clearance (CC) ≥ 50 ml/min determined by 24-hour collection or estimated by Cockcroft-Gault formula

Patients known to be Human Immunodeficiency Virus (HIV)+ are permitted.

Patients with CD4>200 and serum HIV viral load of < 200 copies/mm3 are eligible

HIV+ patients must receive appropriate care and treatment for HIV infection, including antiretroviral medications when clinically indicated, and should be under the care of a physician experienced in HIV management.

HIV testing is not required for eligibility. Must be ≥ 18 years of age.

Must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.

Patient consent must be appropriately obtained in accordance with applicable local and regulatory requirements. Each patient must sign a consent form prior to enrollment in the trial to document their willingness to participate.

Patient is able (i.e. sufficiently fluent) and willing to complete the PRO questionnaires in English or Arabic. The baseline assessment must be completed within required timelines, prior to treatment start. Inability (lack of comprehension in English/Arabic, or other equivalent reason such as cognitive issues or lack of competency) to complete the questionnaires will not make the patient ineligible for the study.

Consent to provision of samples of blood and plasma for correlative studies is optional.

The treatment team must be able to commence definitive RT within 6 weeks of randomization.

Women of child bearing potential must use an accepted and effective method of contraception and/or abstain from sexual intercourse while on protocol treatment and for at least 6 months after the last day of RT. Sexually active males must use an accepted and effective method of contraception and/or abstain from sexual intercourse while on protocol treatment and for at least 6 months after the last day of RT.

Women must not be pregnant or breast-feeding (Women in childbearing period will be instructed by treating physician to avoid pregnancy during and 6 months after end of RT). All females of child bearing potential must have a serum or urine pregnancy test to rule out pregnancy within 4 weeks prior to registration. All breastfeeding women should discontinue breastfeeding prior to study registration.

Participants must not be receiving any other standard anti-cancer therapy or experimental agent concurrently with the study drugs.

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Exclusion Criteria:Patients who fulfill any of the following criteria are not eligible for admission to the study:

HNC Patients with any of the following clinical stages/categories:

cT1-2 N0 M0 cT4 cN3 cM1

Patients with primary oral cavity cancer, nasopharynx cancer, or HNC of unknown primary.

Previous HNC or multiple synchronous primary HNCs.

Previous induction or neo-adjuvant chemotherapy for the study cancer; note that prior chemotherapy for a different cancer is allowable, however, any prior exposure to cisplatin is excluded.

Previous RT to the head and neck or neck dissection of at least 3 levels on either side.

Patients with severe, active co-morbidity including any of the following:

Chronic obstructive pulmonary disease or other pulmonary illness requiring hospitalization within 30 days of registration Unstable angina and/or congestive heart failure requiring hospitalization within 6 months of registration Acute myocardial infarction within 6 months of study registration Diseases precluding RT (e.g. scleroderma) Persistent grade 3-4 (CTCAE v5) electrolyte abnormalities that cannot be reversed despite replacement as indicated by repeat testing Active infection requiring IV antibiotics prior to registration; Chronic renal disease e.g., nephrotic syndrome, that could be worsened by cisplatin therapy History of allogenic organ transplantation Any symptomatic peripheral sensory neuropathy grade ≥ 2 (CTCAE v5)

Prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 3 years (carcinoma in situ of the breast, oral cavity, or cervix are all permissible).

Prior allergic reaction to cisplatin

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Issa Mohamad, Radiation oncologist contact

0799825592

imohamad@KHCC.JO

Ali Hosni, Radiation Onclogsit contact

+416-946_4483

ali.hosni@uhn.ca

Jordan1 site, 1 recruiting
  • King Hussein Cancer Center

    Amman, 11941

    Issa Mohamad, Radiation oncologist, 00962799825592, imohamad@khcc.jo

    Lina Alelaumi, PharmD, 00962796420055, LA.17435@KHCC.JO

    Recruiting

Other trials in Jordan

About this study

Official title: HYperfractionated Radiation Therapy Versus Concurrent Chemoradiation for Head and Neck Cancer (HYTC): A Phase III Randomized Controlled Trial

This is an international multi-centre, non-inferiority phase III randomized controlled trial comparing concurrent chemoradiation with high dose cisplatin (Arm A) vs. hyperfractionated radiation therapy (Arm B) in patients with head and neck squamous cell carcinoma.

Read the detailed description

This is an interventional randomized study in patients with head and neck squamous cell carcinoma , i twill compare between 2 arms (concurrent chemoradiation with high dose cisplatin (Arm A) vs. hyperfractionated radiation therapy (Arm B)

Being tested
70 gy 35 fractions/7weeks+high dose of cisplatin, 81.6 Gy /68 fractions BID FOR 7 WEEKS
Keywords
head and neck squamous cell carcinoma
Medical subject headings
Squamous Cell Carcinoma of Head and Neck

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 70 gy 35 fractions/7weeks+high dose of cisplatinRadiation

    70 Gy 35 fractions/7weeks+high dose of cisplatin

  • 81.6 Gy /68 fractions BID FOR 7 WEEKSRadiation

    81.6 Gy /68 fractions BID FOR 7 WEEKS

Study groups in NCT07801235
Study groupRoleWhat they receive
concurrent ChemoradiationActive comparatorconcurrent chemoradiation with high dose cisplatin (Arm A) ) in patients with head and neck squamous cell carcinoma
Receives: Radiation: 70 gy 35 fractions/7weeks+high dose of cisplatin
hyperfractionated radiation therapyExperimentalhyperfractionated radiation therapy 81.6 Gy
Receives: Radiation: 81.6 Gy /68 fractions BID FOR 7 WEEKS

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. OVERALL SURVIVAL

    To determine if hyperfractionated radiation therapy (Arm B) has a non-inferior overall survival (OS) compared to concurrent chemoradiation (CRT) with high dose cisplatin every 3 weeks (Arm A) in patients with locoregionally advanced head and neck squamous cell carcinoma (HNSCC).

    Measured: 7 YEARS

Secondary outcomes (13)
  1. Oncologic outcomes

    To compare between arms the following:

    Oncologic outcomes: loco-regional failure (LRF)

    Measured: 7 YEARS

  2. Change in hearing threshold levels as assessed by pure tone audiometry

    Hearing threshold levels will be measured using pure tone audiometry across standard audiometric frequencies. Changes from baseline hearing thresholds will be assessed and compared between study groups

    Measured: 7 YEARS

  3. Treatment-related toxicity/adverse events

    Treatment-related toxicity/adverse events: physician-assessed toxicities: National Cancer Institute (NCI) Common Terminology Criteria of Adverse Events (CTCAE) v.5

    Measured: 7 YEARS

  4. Change from baseline in Head and Neck Cancer-specific quality of life as assessed by the University of Washington Quality of Life Questionnaire

    Patient-reported quality of life and swallowing-related quality of life will be assessed using the University of Washington Quality of Life Questionnaire (UW-QOL) . Questionnaire with higher scores indicating better quality of life and swallowing function. Change from baseline scores will be evaluated at predefined study time points

    Measured: 7 YEARS

  5. Distant metastasis (DM) rate between treatment arms

    he occurrence of distant metastases will be assessed and compared between study arms during the study follow-up period

    Measured: From randomisation till 7 years for each study participant

  6. disease-free survival (DFS)

    Disease-free survival (DFS) will be defined as the time from randomization to the first occurrence of disease recurrence (local, regional, or distant) or death from any cause, whichever occurs first

    Measured: 7 years

  7. Change from baseline in ototoxicity severity as assessed by the Modified TUNE grading scale

    Ototoxicity severity will be evaluated using the Modified TUNE grading scale. The scale grades hearing impairment severity based on audiologic assessment findings. Changes from baseline grading scores will be assessed and compared at predefined study time points, with higher grades indicating worse ototoxicity.

    Measured: 7 years

  8. Change from baseline in speech recognition as assessed by Consonant-Nucleus-Consonant (CNC) word scores

    Speech recognition ability will be evaluated using speech audiometry with Consonant-Nucleus-Consonant (CNC) word testing. CNC word scores will be reported as the percentage of correctly identified words, with higher scores indicating better speech recognition performance. Changes from baseline scores will be assessed at predefined study time points

    Measured: 7 years

  9. Number of participants with abnormal tympanometry findings

    Tympanometry will be performed to assess middle ear function. Tympanogram results will be classified according to standard tympanogram types, and the number of participants with abnormal findings will be reported at predefined study time points.

    Measured: 7 years

  10. Treatment-related toxicity/adverse events-PRO

    Treatment-related toxicity/adverse events: patient-reported toxicity: Patient Reported Outcomes - Common Terminology Criteria of Adverse Events (PRO CTCAE) v1.

    Measured: 7 years

  11. Patient-reported outcomes (PRO):UW-QOL

    Patient-reported outcomes (PRO): instrument [University of Washington Quality of Life Questionnaire (UW-QOL)]

    Measured: 7 years

  12. Patient-reported outcomes (PRO): MDADI

    swallowing-related PRO [M.D. Anderson Dysphagia Inventory (MDADI)]

    Measured: 7 Years

  13. Change from baseline in Head and Neck Cancer-specific quality of life as assessed by the M. D. Anderson Dysphagia Inventory (MDADI)

    Patient-reported quality of life and swallowing-related quality of life will be assessed using the M. D. Anderson Dysphagia Inventory (MDADI). Questionnaire with higher scores indicating better quality of life and swallowing function. Change from baseline scores will be evaluated at predefined study time points

    Measured: 7 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Sep 2026
  2. Study start20 Aug 2026
  3. Primary completion1 Apr 2033 (estimated)
  4. Study completion1 Apr 2033 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
604 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07801235
Sponsor's protocol ID
23 KHCC 141
Status last verified
Oct 2026
First submitted
14 Jan 2026
Last updated
14 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing 70 gy 35 fractions/7weeks+high dose of cisplatin and 81.6 Gy /68 fractions BID FOR 7 WEEKS in people with Head and Neck (HNSCC), run by King Hussein Cancer Center at 1 site in Jordan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 14 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Jordan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Issa Mohamad, Radiation oncologist (0799825592, imohamad@KHCC.JO), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

OVERALL SURVIVAL (time frame: 7 YEARS). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Oct 2026.

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