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OncoMatch/Clinical Trials/NCT07801235

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

Is NCT07801235 recruiting? Yes, currently enrolling (Sep 2026). This NA trial studies non-drug interventions for head and neck (hnscc).

NARecruitingKing Hussein Cancer CenterNCT07801235Data as of Sep 2026Location: Jordan

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.

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Extracted eligibility criteria

Cancer type

Head and Neck Squamous Cell Carcinoma

Disease stage

Required: Stage T1 N1-2 M0, T2 N1-2 M0, T3 N0-2 M0 (other)

Excluded: Stage T1 N0 M0, T2 N0 M0

Clinical stage T1-2 N1-2 M0 or T3 N0-2 M0 (UICC/AJCC TNM 8th Edition). Excluded: cT1-2 N0 M0, cT4, cN3, cM1

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

Cannot have received: induction or neoadjuvant chemotherapy for the study cancer

Previous induction or neo-adjuvant chemotherapy for the study cancer; note that prior chemotherapy for a different cancer is allowable

Cannot have received: cisplatin (cisplatin)

any prior exposure to cisplatin is excluded

Cannot have received: radiation therapy to the head and neck

Previous RT to the head and neck

Cannot have received: neck dissection of at least 3 levels on either side

neck dissection of at least 3 levels on either side

Lab requirements

Blood counts

Hemoglobin > 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.

Kidney function

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

Liver function

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 hematologic, hepatic, and renal function must be documented within 8 weeks prior to registration

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07801235 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior induction or neoadjuvant chemotherapy for the study cancer, cisplatin, radiation therapy to the head and neck disqualifies patients from enrollment.

What disease stage is eligible?

Stage T1 N1-2 M0 or T2 N1-2 M0 or T3 N0-2 M0 is required.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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