University of Rochester, Dept. Radiation Oncology
Rochester, New York, 14642, United States
NCT Number: NCT00178230
This study is being conducted by the University of Rochester Cancer Center to determine the levels of cytokines in the blood, and to determine if blood levels of these cytokines are related to the side effects of radiation therapy combined with other treatments.
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Notify Me18 year and older
All sexes
Observational
Rochester, New York, 14642, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients receiving radiation therapy for lung cancer combined with surgery either pre or post RT to the chest for lung cancer not associated with atelectasis, pleural effusion.
Patients receiving HDR Brachytherapy for lung cancer.
Patients receiving concomitant radiation and interferon therapy for lung cancer.
Patients receiving concomitant chemotherapy and radiation for lung cancer. Prior drug therapy does not make patients ineligible.
Karnofsky ≥ 70 %.
There are no age restrictions.
Acceptable bone marrow function - WBC 2 3000/mm3, platelet count > 100,000, hematocrit ≥ 33%, hemoglobin ≥ 11 gms/dl.
Life expectancy > 6 months.
Patients must sign informed consent meeting all federal and institutional guidelines.
Exclusion criteria
Patients not meeting eligibility criteria stated above
University of Rochester
Other
Circulating Cytokines as Predictors of Radiation Induced Pulmonary Toxicity in Thoracic Malignancies
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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