NCT03649048Recruiting
Low-Dose Weekly vs High-Dose Cisplatin
Randomized Trial Comparing Low-Dose Weekly to High-Dose Cisplatin Concurrent With Radiation for Locally Advanced Head and Neck Cancer.
Source: ClinicalTrials.gov · Last updated 31 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
This study is a prospective open-label randomized clinical trial. Following informed consent eligible LASCCHN patients (n=100) planned for CRT will be stratified by tumor p16 status and then randomized in a 1:1 fashion to either concurrent HD cisplatin or concurrent weekly LD cisplatin.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- First submitted
- 29 Jun 2018
- Start date
- 5 Nov 2018
- Primary completion date
- 30 Sept 2028
- Lead sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
- Diseases
- Head and neck cancer
- NCT number
- NCT03649048
What you commit to
- Study type: Interventional
- Planned participants: 100
- From 5 Nov 2018 to the primary completion date, 30 Sept 2028
- 3 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Serious medical comorbidities or other contraindications to radiotherapy and/or chemotherapy.
- Prior history of head and neck cancer within 5 years.
- Prior or planned neoadjuvant chemotherapy prior to CRT.
- Prior head and neck radiation at any time.
- Inability to attend full course of radiotherapy or follow-up visits.
Other illness
- Distant metastatic disease.
- Prior invasive malignant disease unless disease-free for at least 5 years or more, with the exception of non-melanoma skin cancer or in-situ carcinoma.
Other
- Nasopharyngeal primary confirmed or suspected.
- Severe hearing loss as determined clinically Pre-existing use of hearing aids.
- Peripheral neuropathy .grade 2 (CTCAE v4.02).
- Unable or unwilling to complete QOL questionnaires.
- Pregnant or lactating women.
- Unable to use dual method of contraception.
Who the study is looking for
- Age 18 or older
- Willing and able to provide written informed consent
- Eastern Cooperative Oncology Group (ECOG) performance status 0-2
- Histologically or cytologically confirmed squamous cell carcinoma
- Primary tumor site includes oral cavity, oropharynx, nasal cavity, salivary glands (excluding parotid), hypopharynx, or larynx and primary unknown
- Patients must be deemed suitable for HD cisplatin therapy based on tumor characteristics, clinical condition and comorbidities in the judgement of the treating medical oncologist.
- Patients must be planned to receive radical intent radiation treatment based on clinical condition, comorbidities and tumor characteristics in the judgment of the treating radiation oncologist
- Adequate organ and marrow function independent of transfusion for at least 7 days prior to randomization defined as:
- Hemoglobin \> 80 g/L; Absolute neutrophil count \>1.5x10⁹ /L, platelets \>100x10⁹/L; Bilirubin \< 35 umol/L; AST or ALT \< 3 x the upper limit of normal; Calculated creatinine clearance (as determined by Cockcroft- Gault) \> 50 ml/min
- Males:
- Creatinine Clearance = Weight (kg) x (140 - Age) (mL/min) 72 x serum creatinine (mg/dL)
- Females:
- Creatinine Clearance = Weight (kg) x (140 - Age) x 0.85 (mL/min) 72 x serum creatinine (mg/dL)
- Patient must be assessed at head and neck cancer multidisciplinary clinic (with assessment by radiation oncologist and surgeon) and presented at multidisciplinary tumor board prior to randomization.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Juravinski Cancer Centre Coordinator of this site? Confirm its status | Hamilton | Canada | Recruiting |
| London Regional Cancer Program Coordinator of this site? Confirm its status | London | Canada | Active, not recruiting |
| Sunnybrook Health Sciences Centre Coordinator of this site? Confirm its status | Toronto | Canada | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.