New scan may predict lung cancer outcomes
NCT ID NCT07316309
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether a new type of PET/CT scan can help predict how well treatment will work for people with a certain type of lung cancer (limited-stage small cell lung cancer). 33 participants had the scan before starting standard treatment. Researchers then tracked their cancer progression to see if the scan results could forecast outcomes. The goal is to better understand which patients might need more or less aggressive treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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33 people
The number who actually took part.
- Started
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Nov 2022
- Finished
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Sep 2025
- 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
Adult patients with newly diagnosed, histopathologically confirmed limited-stage small cell lung cancer who underwent baseline \[18F\]AlF-NOTA-QHY-04 PET/CT imaging prior to concurrent chemoradiotherapy at Shandong Cancer Hospital and Institute.
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Histopathologically confirmed limited-stage small cell lung cancer (T1-4N0-3M0) according to the AJCC TNM 8th edition. * Age ≥ 18 years. * Eastern Cooperative Oncology Group (ECOG) performance status of 0-1. * Presence of measurable disease according to RECIST version 1.1. * Newly diagnosed patients who had not received any prior anticancer treatment. * Underwent baseline \[18F\]AlF-NOTA-QHY-04 PET/CT imaging prior to treatment. Exclusion Criteria: * Presence of autoimmune diseases or active comorbid infections. * Pregnancy or breastfeeding. * Unable or unwilling to provide informed consent.
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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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Shandong Cancer Hospital and Institute
Jinan, Shandong, 250117, China
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Other studies related to the condition(s) this trial covers.
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