Blood test reveals why lung cancer drugs stop working
NCT ID NCT03833934
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 62 people with ALK-positive lung cancer whose tumors had stopped responding to newer targeted drugs. Instead of a tissue biopsy, researchers used a blood test (liquid biopsy) to find genetic changes that cause resistance. The goal was to better understand these mutations and help doctors choose the next treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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62 people
The number who actually took part.
- Started
-
Jan 2019
- Finished
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Oct 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
This research study is for lung cancer patients with ALK-positive lung cancer who had been on a newer ALK targeted treatment (such as ceritinib, alectinib, brigatinib, or larlatinib).
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Men or women older than 18 years at the time of consent. * Demonstration of having advanced ALK positive NSCLC. * Systemic progression (not CNS only progression) within the past 30 days while receiving a next generation ALK TKI. * Patient must not have started a new line of therapy before signing the informed consent form. * Willingness to provide a blood specimen prior to the initiation of a new line of treatment. * Willing to provide clinical and medical information to the study team as required. * Ability to read, write and communicate in English. * Ability to sign a web-based informed consent form. Exclusion Criteria: * Participants who are unable to provide informed consent. * Participants who are 18 years of age or younger. * Participants who are unable to comply with the study procedures. * Known existence of an uncontrolled intercurrent illness including, but not limited to, psychiatric illness or social situations that would impair compliance with study requirements. * Participants who have previously enrolled to the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Dana-Farber Cancer Institute
Boston, Massachusetts, 02215, United States
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Other studies related to the condition(s) this trial covers.
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