CApecitabine Prior to TUmor Resection in Ent Oncology (CAPTURE)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Capecitabine, Standard of Care (SOC).
- Who it may be relevant to
- Registry conditions: Head Neck Cancer, Mouth Cancer, Throat Cancer, Larynx Cancer. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
head and neck squamous cell carcinoma (HNSCC) is a type of cancer that affects areas such as the mouth, throat, and voice box. Despite medical progress, little has changed in the care for patients with HPV-negative cancer. The standard care involves surgery followed by radiation or chemotherapy if needed. However, delays in starting treatment - especially beyond six weeks - are linked to worse outcomes. Many patients also experience cancer returning within two years, often making it harder to treat. This study aims to improve outcomes by giving patients a short course of capecitabine, a chemotherapy pill, before surgery. Capecitabine is easier to tolerate than traditional intravenous chemotherapy and has shown promising results in shrinking tumors. Researchers believe that starting this oral treatment early could reduce delays, shrink tumors, make surgery less complex, and improve survival. The clinical trial will randomly assign patients with newly diagnosed stage III or IVa HPV-negative head and neck cancer to receive either standard care or capecitabine before surgery. Surgery will be performed within six weeks of diagnosis, followed by additional therapy as needed. The study will measure how well the tumor responds under the microscope after surgery, how much it shrinks on scans, the safety of the treatment, and cancer-free survival at two years. It will also explore biological markers linked to treatment response. If successful, this approach could offer a simpler, faster, and more effective way to treat head and neck cancer, leading to earlier treatment, less invasive surgery, and improved patient outcomes. The study plans to include about 62 patients to evaluate the benefits of this new treatment strategy
Interventions
- Drug Capecitabine
Patients will receive fixed-dose capecitabine prior to surgery - Other Standard of Care (SOC)
Standard of care (no intervention until surgery)
Primary outcome measures
- Pathologic response [Time frame: From initiation of capecitabine to surgery]
Secondary outcome measures (1)
- Treatment toxicity (grade 3 or greater) [Time frame: Within first 60 days of treatment initiation]
Eligibility criteria
Inclusion criteria
- • Previously untreated, histologically confirmed non-HPV related HNSCC and radiologically or histologically confirmed stage I or IVA (AJCC 8th edition).
- No evidence of distant metastatic disease.
- Able to undergo protocol therapy, including necessary imaging and surgery.
- If female: may participate if not actively pregnancy nor breastfeeding.
- If male: must agree to refrain from donating sperm and must either be abstinent or agree to use contraception.
- Performance status (ECOG) of 0, 1 or 2.
Exclusion criteria
- History of immunodeficiency, HBV, HCV, HIV. No HBV, HCV or HIV testing is required unless mandated by local health authority.
- Active infection requiring systemic therapy.
- Previous allogenic tissue/solid organ transplant.
- Known severe hypersensitivity (≥ Grade 3) to capecitabine, its active substance and/or any of its excipients.
- History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the participant's participation for the full duration of the trial, or is not in the best interest of the participant to participate, in the opinion of the treating investigator.
- Known DYPD mutation.
- Known psychiatric or substance abuse disorders that would interfere with cooperating with the requirements of the trial.
- Received prior systemic anticancer therapy including investigational agents for the current malignancy prior to allocation.
- Currently participating in or has participated in a trial of an investigational agent or has used an investigational device within 4 weeks prior to the first dose of trial treatment.
- Known additional malignancy that is progressing or requires active treatment within the past (5 years), excluding basal cell carcinoma or cutaneous squamous cell carcinoma.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07254962 · MP-37-2026-12048