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Clinical Trial Finder

Search Results

Observation or Upfront Cranial RT in Oncogene Mutated NSCLC With Asymptomatic BM: A Phase III RCT

Study Purpose

Tyrosine Kinase Inhibitors (TKIs) especially higher generation TKI have higher CNS penetration rates and have shown favorable response rates in brain metastases. Brain radiotherapy/surgery is the standard treatment in brain metastases especially symptomatic metastases, however, the role of local treatment especially in driver mutation-positive non-small cell lung cancer with asymptomatic brain metastases is being questioned given their potential side effects. No randomized trial has shown the superiority of early vs.#46; delayed cranial RT in asymptomatic BM of driver mutated NSCLC.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Interventional
Eligible Ages 18 Years - 99 Years
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

1. Age ≥ 18 years. 2. Patients with ECOG performance status of 0-2. 3. Patients with pathologically proven diagnosis of NSCLC. 4. Patients with positive oncogene mutation status (EGFR/ALK) 5. Patients with radiologically confirmed parenchymal brain metastases. 6. Patients with asymptomatic Synchronous or Metachronous brain metastases. 7. Patients willing for written informed consent and must be willing to comply with the specified follow-up schedule.

Exclusion Criteria:

1. Patients with CSF dissemination only without any parenchymal brain metastases. 2. Patients with brain metastases in the brain stem. 3. Patients with prior history of radiation therapy to the brain. 4. Patient not suitable for TKI therapy as per the medical oncologist. 5. Pregnant or lactating females

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT05236946
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

Phase 3
Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

Tata Memorial Hospital
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

N/A
Principal Investigator Affiliation N/A
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Other
Overall Status Recruiting
Countries India
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Asymptomatic Brain Metastases, Driver Mutation Positive Non-small Cell Lung Cancer
Arms & Interventions

Arms

Active Comparator: Upfront Cranial Radiotherapy

Stereotactic radiosurgery or Whole brain radiotherapy upfront in asymptomatic brain metastases

Experimental: Observation (Delayed Cranial Radiotherapy)

Observation (Delayed Cranial radiotherapy) of Asymptomatic brain metastases

Interventions

Radiation: - Stereotactic radiosurgery/whole brain radiotherapy

SRS/ WBRT for asymptomatic brain metastases depending on the number of brain metastases

Drug: - Tyrosine kinase inhibitor

TKI

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

International Sites

Tata Memorial Hospital, Mumbai, Maharashtra, India

Status

Recruiting

Address

Tata Memorial Hospital

Mumbai, Maharashtra, 400012

Site Contact

Dr. Anil Tibdewal, MD

[email protected]

9122 2417 7000

Nearest Location

Site Contact

Dr. Anil Tibdewal, MD

[email protected]

9122 2417 7000


Resources

  • Patient and Caregiver Survey
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The content provided on clinical trials is for informational purposes only and is not a substitute for medical consultation with your healthcare provider. We do not recommend or endorse any specific study and you are advised to discuss the information shown with your healthcare provider. While we believe the information presented on this website to be accurate at the time of writing, we do not guarantee that its contents are correct, complete, or applicable to any particular individual situation. We strongly encourage individuals to seek out appropriate medical advice and treatment from their physicians. We cannot guarantee the availability of any clinical trial listed and will not be responsible if you are considered ineligible to participate in a given clinical trial. We are also not liable for any injury arising as a result of participation.

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