PMID- 11917281 OWN - NLM STAT- MEDLINE DCOM- 20020418 LR - 20240109 IS - 1053-4296 (Print) IS - 1053-4296 (Linking) VI - 12 IP - 1 Suppl 1 DP - 2002 Jan TI - Radiation pneumonitis and early circulatory cytokine markers. PG - 26-33 AB - Radiation pneumonitis is a distinct clinical entity that differs from other pulmonary symptoms such as allergic pneumonitis, chemical pneumonitis, or pneumonia by various infectious agents. Recent research has supported the mechanism of cellular interaction between lung parenchymal cells and circulating immune cells mediated through a variety of cytokines including proinflammatory cytokines, chemokines, adhesion molecules, and profibrotic cytokines. Identifying reliable biomarkers for radiation pneumonitis will allow us to identify individuals at risk for pneumonitis before or during the early stage of therapy. Prospective blood sampling, scoring of respiratory symptoms, and chest imaging were conducted for patients receiving thoracic radiotherapy for malignancy. Serial plasma specimens were analyzed for circulating cytokine changes before, during, and up to 12 weeks after radiation. Radiation pneumonitis was diagnosed using National Cancer Institute (NCI) common toxicity criteria. Cytokine analysis was assayed for interleukin 1alpha (IL-1alpha), interleukin 6 (IL-6), monocyte chemotactic protein 1 (MCP-1), E-selectin, L-selectin, transforming growth factor beta1 (TGF-beta1), and basic fibroblast growth factor (bFGF) using enzyme linked immmunosorbant assay (ELISA). Twenty-four patients had clinical follow-up longer than 12 months after radiotherapy. Thirteen had symptomatic pneumonitis (NCI grade 2). The peak incidence of symptoms was between 6 and 13 weeks after radiotherapy. Six patients had only radiographic infiltrates (NCI grade 1). Five patients did not have clinical or radiographic pneumonitis. Both IL-1alpha and IL-6 levels were significantly higher before, during, and after radiotherapy for those who had pneumonitis. The pattern of changes of MCP-1, E-selectin, L-selectin, TGF-beta1, and bFGF varied, but none of these cytokines correlated with radiation pneumonitis. Analysis of a panel of circulating cytokines with different putative functions in radiation pulmonary injury identified IL-1alpha and IL-6 as early circulating cytokine markers for radiation pneumonitis. CI - Copyright 2002, Elsevier Science (USA). All rights reserved. FAU - Chen, Yuhchyau AU - Chen Y AD - Department of Radiation Oncology, James P. Wilmot Cancer Center, University of Rochester, Rochester, NY 14642, USA. FAU - Williams, Jacqueline AU - Williams J FAU - Ding, Ivan AU - Ding I FAU - Hernady, Eric AU - Hernady E FAU - Liu, Weimin AU - Liu W FAU - Smudzin, Therese AU - Smudzin T FAU - Finkelstein, Jacob N AU - Finkelstein JN FAU - Rubin, Philip AU - Rubin P FAU - Okunieff, Paul AU - Okunieff P LA - eng GR - P-01 CA11051-26/CA/NCI NIH HHS/United States GR - R-01 CA27791-15/CA/NCI NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Semin Radiat Oncol JT - Seminars in radiation oncology JID - 9202882 RN - 0 (Biomarkers) RN - 0 (Cytokines) RN - 0 (Interleukin-1) RN - 0 (Interleukin-6) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Biomarkers/blood MH - Cytokines/*blood MH - Enzyme-Linked Immunosorbent Assay MH - Female MH - Humans MH - Interleukin-1/blood MH - Interleukin-6/blood MH - Male MH - Middle Aged MH - Radiation Pneumonitis/blood/*diagnosis MH - Risk Factors MH - Thoracic Neoplasms/*radiotherapy EDAT- 2002/03/28 10:00 MHDA- 2002/04/19 10:01 CRDT- 2002/03/28 10:00 PHST- 2002/03/28 10:00 [pubmed] PHST- 2002/04/19 10:01 [medline] PHST- 2002/03/28 10:00 [entrez] AID - asrao012b00s26 [pii] AID - 10.1053/srao.2002.31360 [doi] PST - ppublish SO - Semin Radiat Oncol. 2002 Jan;12(1 Suppl 1):26-33. doi: 10.1053/srao.2002.31360.