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dc.contributor.authorTopkan, Erkan
dc.contributor.authorSelek, Ugur
dc.contributor.authorOzdemir, Yurday
dc.contributor.authorBesen, Ali A.
dc.contributor.authorGuler, Ozan C.
dc.contributor.authorYildirim, Berna A.
dc.contributor.authorMertsoylu, Huseyin
dc.contributor.authorFindikcioglu, Alper
dc.contributor.authorOzyikan, Ozgur
dc.contributor.authorPehlivan, Berrin
dc.date.accessioned2019-05-03T12:55:48Z
dc.date.available2019-05-03T12:55:48Z
dc.date.issued2018
dc.identifier.issn1687-8450
dc.identifier.urihttps://www.hindawi.com/journals/jo/2018/4518935/abs/
dc.identifier.urihttp://hdl.handle.net/11727/3128
dc.description.abstractWe aimed to identify the fatal pulmonary hemorrhage- (FPH-) related risk factors in stage 3B/C squamous-cell lung carcinoma (SqCLC) patients treated with definitive concurrent chemoradiotherapy (C-CRT). Medical records of 505 stage 3B/C SqCLC patients who underwent 66 Gy radiotherapy plus 1-3 cycles of concurrent chemotherapy with available pretreatment thoracic computerized tomography scans were retrospectively analyzed. Primary end-point was the identification of FPH-related risk factors. Examined factors included the basal patient and tumor characteristics with specific emphasis on the tumor cavitation (TC) status, tumor size (TS) and cavitation size (CS), tumor volume and cavitation volume (TV and CV), relative cavitation size (RCS = CS/Ts), and relative cavitation volume (RCV=CV/TV). FPH emerged in 13 (2.6%) patients, with 12 (92.3%) of them being diagnosed <= 12 months of C-CRT. All FPHs were diagnosed in patients with TC (N=60): group-specific FPH incidence: 21.6%. TC (P<0.001) was the unique independent factor associated with higher FPH risk in multivariate analysis. Further analysis limited to TC patients exhibited the RCV>0.14 (37.5% versus 11.1% for RCV <= 0.14; P<0.001), major RCS group (31.0% versus 19.0% for minor versus 0% for minimum RCS; P-0.008), and baseline hemoptysis (26.3% versus 13.6% for no hemoptysis; P-0.009) as the independent risk factors for higher FPH incidence. FPH was an infrequent (2.6%) complication of C-CRT in stage 3B/C SqCLC patients, but its incidence increased to 37.5% in patients presenting with TC and RCV>0.14. Diagnosis of >90% FPHs <= 12 months of C-CRT stresses the importance of close and careful follow-tip of high-risk patients after C-CRT for multidisciplinary discussion of possible invasive preventive measures.en_US
dc.language.isoengen_US
dc.relation.isversionof10.1155/2018/4518935en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBODY RADIATION-THERAPYen_US
dc.subjectRANDOMIZED PHASE-IIIen_US
dc.subjectMASSIVE HEMOPTYSISen_US
dc.subjectCANCER-PATIENTSen_US
dc.subjectRADIOTHERAPYen_US
dc.subjectTRIALen_US
dc.subjectBRACHYTHERAPYen_US
dc.subjectBEVACIZUMABen_US
dc.subjectCHEMORADIATIONen_US
dc.subjectCHEMOTHERAPYen_US
dc.titleRisk Factors for Fatal Pulmonary Hemorrhage following Concurrent Chemoradiotherapy in Stage 3B/C Squamous-Cell Lung Carcinoma Patientsen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF ONCOLOGYen_US
dc.identifier.wos000449930000001en_US
dc.identifier.scopus2-s2.0-85062639690en_US
dc.contributor.pubmedID30515211en_US
dc.contributor.orcID0000-0001-6908-3412en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.contributor.researcherIDAAC-5654-2020


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