Prophylactic Cranial Irradiation in Patients With Lung Adenocarcinoma With High Risk of Brain Metastasis
NCT ID: NCT01603849
Last Updated: 2023-04-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
84 participants
INTERVENTIONAL
2012-05-31
2020-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Radical Treatment of Synchronous Oligometastatic Non-Small Cell Lung Carcinoma
NCT02805530
Brain Irradiation in Treating Patients With Limited-Stage Small Cell Lung Cancer
NCT00057746
Radiation Therapy in Treating Patients With Extensive Stage Small Cell Lung Cancer
NCT01055197
Predictors of Radiation Pneumonitis in Locally Advanced Lung Cancer Treated With Chemoradiation
NCT01580579
Radiation Therapy to Prevent Brain Metastases in Patients With Previously Treated Extensive-Stage Small Cell Lung Cancer
NCT00016211
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
1. To obtain a greater PFS and CNS PFS in patients with NSCLC treated with PCI after locoregional or systemic treatment.
2. Evaluate the benefit in OS in the specific group of patients who are at increased risk of developing brain metastasis
3. Evaluate quality of life and mental function before and after treatment with PCI and compare it with patients in the observation group.
Methods: One hundred and twenty eight patients with locally advanced or metastatic (except CNS metastasis) NSCLC will be included and randomized to receive either observation or PCI 25 Gy in 10 fractions Whole Brain Radiotherapy (WBRT) once the initial treatment has been completed and progression of the disease ruled out.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
A Prophylactic Cranial Irradiation
Patients will received PCI 25 Gy in 10 fractions WBRT 4 weeks after initial treatment in the absence of disease progression.
Prophylactic Cranial Irradiation
Patients allocated to this arm will received treatment with whole brain radiotherapy 25 Gy in 10 fractions.
B Observation Group
Patients in this arm will be observed (not receiving WBRT)
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Prophylactic Cranial Irradiation
Patients allocated to this arm will received treatment with whole brain radiotherapy 25 Gy in 10 fractions.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Above 18 years
* General status with a Karnofsky \>80%
* Eastern Cooperative Group (ECOG) ≤2
* Negative CNS MRI at the beginning of any treatment
* Carcinoembryonic antigen \> 20 pg
* Hepatic and hematic cytology test within normal range
* Adequate renal function
* Those who accepted to participate in the study and who sign the letter of informed consent.
Exclusion Criteria
* Patients who refuse participate in the protocol
* General status with a Karnofsky \<80%
* Eastern Cooperative Group (ECOG) \>2
* Previous treatment with WBRT
* Previous treatment with chemotherapy
* Disease progression after initial treatment, either chemotherapy or chemoradiotherapy depending the case.
* CNS metastasis at diagnosis
* Abnormal laboratory test that interfere with chemotherapy or TKI administration
18 Years
60 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Instituto Nacional de Cancerologia de Mexico
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Oscar Gerardo Arrieta Rodríguez
Head of Lung Cancer Clinic
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Oscar MD Arrieta, MD
Role: PRINCIPAL_INVESTIGATOR
Instituto Nacional de Cancerologia, Columbia
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Instituto Nacional de Cancerología
Mexico City, , Mexico
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Arrieta O, Maldonado F, Turcott JG, Zatarain-Barron ZL, Barron F, Blake-Cerda M, Cabrera-Miranda LA, Cardona AF, de la Garza JG, Rosell R. Prophylactic Cranial Irradiation Reduces Brain Metastases and Improves Overall Survival in High-Risk Metastatic Non-Small Cell Lung Cancer Patients: A Randomized phase 2 Study (PRoT-BM trial). Int J Radiat Oncol Biol Phys. 2021 Aug 1;110(5):1442-1450. doi: 10.1016/j.ijrobp.2021.02.044. Epub 2021 Feb 25.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
pciHighRiskINCAN
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.