NCT06238882Recruiting
Nitroglycerin Plus Radiotherapy Versus Conventional Radiotherapy in Patients With Lung Cancer.
A Phase III Study Comparing Concurrent Nitroglycerin With Radiation Therapy vs Radiation Therapy Alone in Patients With Non-small Cell Lung Cancer With EGFR Mutations and Brain Metastases.
Source: ClinicalTrials.gov · Last updated 9 Apr 2026
Brief summary (registry, in English)
The goal of this interventional phase III clinical trial is to evaluate objective intracranial response rate (iORR) after a treatment with total cranial radiation therapy plus concomitant transdermal nitroglycerin (NTG) addition or total cranial radiation therapy only in patients with stage IV non-small cell lung cancer with brain metastases and EGFR mutation. The main questions it aims to answer are: Determine progression-free survival (PFS) to CNS and overall survival (OS). Evaluate and compare the quality of life (QoL) of patients during and after treatment. Evaluate the cognitive function of patients before, during and after treatment. Evaluate treatment-associated toxicity to grade adverse treatment events Evaluation of HIF1α, VEGF and ROS1 in peripheral blood before and after nitroglycerin treatment. All participants will have laboratory tests at the beginning and end of radiation therapy. Cranial MRI will be performed prior to treatment and 12 weeks after the end of treatment, then every 16 weeks until intracranial progression. Patients in the interventional group will be given 36 mg patches of transdermal nitroglycerin for 24 hours with a 12-hour rest interval during treatment with radiation therapy. The control group will only receive total cranial radiation therapy at the same doses and with the same schedule.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 74 (estimated)
- First submitted
- 22 Jan 2024
- Start date
- 23 Feb 2023
- Primary completion date
- 23 Dec 2026
- Lead sponsor
- Instituto Nacional de Cancerologia de Mexico
- Diseases
- Lung cancer
- NCT number
- NCT06238882
What you commit to
- Study type: Interventional
- Planned participants: 74
- From 23 Feb 2023 to the primary completion date, 23 Dec 2026
- 1 site 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
- Any other malignant pathology within the previous 5 years (except for cervical carcinoma in situ or basal-cell skin cancer, treated appropriately).
Other illness
- Any unstable systemic disease (including active infection, grade 4 hypertension, unstable angina, congestive heart failure, ischemic heart disease, liver, kidney disease).
- Patients with a history of allergy to glyceryl tinistate
- Failure to follow protocol rules.
Other
- Pregnant and/or breastfeeding women.
- Meningeal carcinomatosis corroborated by cytopathological study.
- Disposal Criteria:
- Loss of patient follow-up.
- Patients who express their desire not to continue the study.
- Patients with unacceptable toxicity
Who the study is looking for
- Patients diagnosed with advanced non-small cell lung cancer (which includes de novo stage IIIB-IV, according to the 8th edition AJCC, or recurrent disease), documented by histology and/or cytology.
- Presence of brain metastases, candidates for treatment with holocranial radiation therapy.
- Documented EGFR sensitivity mutation.
- Disease measurable by criteria: The Response Assessment in Neuro-Oncology Brain Metastases (RANO-BM).
- 18 years and up.
- Functional status, by ECOG scale 0-2
- Life expectancy at least 12 weeks.
- Not receive vasodilator treatment as calcium channel blockers.
- Electrocardiogram
- Neutrophil count 1.5 x 103/mm3, platelet count \>100 x (103/mm3).
- Serum bilirubin should be 1.5 of the upper normal limit (ULN, upper normal limit).
- AST and/or ALT 2 ULN (or 5 x ULN in patients with liver metastases).
- Serum creatinine 1.5 (ULN), or creatinine clearance 60ml/min.
- Ability to comply with study and follow-up procedures.
- Informed written (signed) consent to participate in the study.
- Have tumor tissue (paraffin blocks from diagnostic biopsy) obtained before systemic treatment
Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Instituto Nacional de Cancerologia Coordinator of this site? Confirm its status | Mexico City | Mexico | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.