Safety and Palliative Efficacy of Single-Dose 8-Gy Reirradiation for Painful Local Failure in Patients with Stage IV Non-Small Cell Lung Cancer Previously Treated with Radical Chemoradiation Therapy

dc.contributor.authorTopkan, Erkan
dc.contributor.authorYildirim, Berna Akkus
dc.contributor.authorGuler, Ozan Cem
dc.contributor.authorParlak, Cem
dc.contributor.authorPehlivan, Berrin
dc.contributor.authorSelek, Ugur
dc.contributor.orcID0000-0001-8120-7123en_US
dc.contributor.orcID0000-0001-6170-0383en_US
dc.contributor.orcID0000-0001-6661-4185en_US
dc.contributor.orcID0000-0001-6908-3412en_US
dc.contributor.orcID0000-0001-8087-3140en_US
dc.contributor.pubmedID25752391en_US
dc.contributor.researcherIDAAG-2213-2021en_US
dc.contributor.researcherIDB-3671-2014en_US
dc.contributor.researcherIDV-5717-2017en_US
dc.contributor.researcherIDAAC-5654-2020en_US
dc.contributor.researcherIDO-5474-2014en_US
dc.date.accessioned2024-02-23T11:53:24Z
dc.date.available2024-02-23T11:53:24Z
dc.date.issued2015
dc.description.abstractPurpose: To investigate the safety and efficacy of single-dose 8-Gy palliative chest reirradiation (CRI) in metastatic non-small cell lung cancer (M-NSCLC) patients with painful thoracic failures (TF) within the previous radiation portal. Patients and Methods: We retrospectively analyzed the clinical data of 78 M-NSCLC patients who received single-dose 8-Gy CRI for painful TF after concurrent chemoradiation therapy to a total radiation dose of 52 to 66 Gy between 2007 and 2012. Primary endpoints included significant pain relief (SPR) defined as a >= 2 point decrement in the Visual Analogue Scale for Pain inventory (VAS-P), time to pain relief, and duration of pain control. Secondary objectives were survival and prognostic factors. Results: Treatment was well tolerated, with only 5.1% grade 3 pneumonitis and 1.3% grade 2 esophagitis. Pre-CRI median and post-CRI minimum VAS-P were 7 and 3 (P < .001), respectively. SPR was noted in 67 (85.9%) patients, and only 3 (3.9%) scored progressive pain. Median time to lowest VAS-P and duration of pain control were 27 days and 6.1 months, respectively. Median overall survival (OS) was 7.7 months, and the 1-year OS rate was 26.5%. On multivariate analyses, lower Eastern Cooperative Oncology group score (1-2; P < .001), absence of anemia (P = .001), and fewer metastatic sites (1-2; P < .001) were found to be associated with longer OS. Conclusions: Single-dose 8-Gy CRI provides safe, effective, and durable pain palliation for TF in radically irradiated M-NSCLC patients. Because of its convenience, lower cost, and higher comfort, the present protocol can be considered an appropriate option for patients with limited life spans. (C) 2015 Elsevier Inc.en_US
dc.identifier.eissn1879-355Xen_US
dc.identifier.endpage780en_US
dc.identifier.issn0360-3016en_US
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-84924678251en_US
dc.identifier.startpage774en_US
dc.identifier.urihttp://hdl.handle.net/11727/11592
dc.identifier.volume91en_US
dc.identifier.wos000351733500017en_US
dc.language.isoengen_US
dc.relation.isversionof10.1016/j.ijrobp.2014.12.010en_US
dc.relation.journalINTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICSen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEXTERNAL-BEAM RADIOTHERAPYen_US
dc.subjectRADIATION-THERAPYen_US
dc.subjectCONCURRENT CHEMORADIATIONen_US
dc.subjectTHORACIC REIRRADIATIONen_US
dc.subjectPHASE-IIIen_US
dc.subjectIRRADIATIONen_US
dc.subjectCARCINOMAen_US
dc.subjectRETREATMENTen_US
dc.subjectRECURRENCEen_US
dc.subjectOUTCOMESen_US
dc.titleSafety and Palliative Efficacy of Single-Dose 8-Gy Reirradiation for Painful Local Failure in Patients with Stage IV Non-Small Cell Lung Cancer Previously Treated with Radical Chemoradiation Therapyen_US
dc.typeArticleen_US

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