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dc.contributor.authorSalama, Joseph K.
dc.contributor.authorStinchcombe, Thomas E.
dc.contributor.authorGu, Lin
dc.contributor.authorWang, Xiaofei
dc.contributor.authorMorano, Karen
dc.contributor.authorBogart, Jeffrey A.
dc.contributor.authorCrawford, Jeffrey C.
dc.contributor.authorSocinski, Mark A.
dc.contributor.authorBlackstock, A. William
dc.contributor.authorVokes, Everett E.
dc.date2022-08-11T08:10:45.000
dc.date.accessioned2022-08-23T17:18:50Z
dc.date.available2022-08-23T17:18:50Z
dc.date.issued2011-11-15
dc.date.submitted2014-01-25
dc.identifier.citationInt J Radiat Oncol Biol Phys. 2011 Nov 15;81(4):e269-74. doi: 10.1016/j.ijrobp.2011.01.056. Epub 2011 Apr 7. <a href="http://dx.doi.org/10.1016/j.ijrobp.2011.01.056">Link to article on publisher's site</a>
dc.identifier.issn0360-3016 (Linking)
dc.identifier.doi10.1016/j.ijrobp.2011.01.056
dc.identifier.pmid21477940
dc.identifier.urihttp://hdl.handle.net/20.500.14038/47941
dc.description.abstractPURPOSE: Cancer and Leukemia Group B (CALGB) 30105 tested two different concurrent chemoradiotherapy platforms with high-dose (74 Gy) three-dimensional conformal radiotherapy (3D-CRT) after two cycles of induction chemotherapy for Stage IIIA/IIIB non-small cell lung cancer (NSCLC) patients to determine if either could achieve a primary endpoint of >18-month median survival. Final results of 30105 demonstrated that induction carboplatin and gemcitabine and concurrent gemcitabine 3D-CRT was not feasible because of treatment-related toxicity. However, induction and concurrent carboplatin/paclitaxel with 74 Gy 3D-CRT had a median survival of 24 months, and is the basis for the experimental arm in CALGB 30610/RTOG 0617/N0628. We conducted a secondary analysis of all patients to determine predictors of treatment-related pulmonary toxicity. METHODS AND MATERIALS: Patient, tumor, and treatment-related variables were analyzed to determine their relation with treatment-related pulmonary toxicity. RESULTS: Older age, higher N stage, larger planning target volume (PTV)1, smaller total lung volume/PTV1 ratio, larger V20, and larger mean lung dose were associated with increasing pulmonary toxicity on univariate analysis. Multivariate analysis confirmed that V20 and nodal stage as well as treatment with concurrent gemcitabine were associated with treatment-related toxicity. A high-risk group comprising patients with N3 disease and V20 >38% was associated with 80% of Grades 3-5 pulmonary toxicity cases. CONCLUSIONS: Elevated V20 and N3 disease status are important predictors of treatment related pulmonary toxicity in patients treated with high-dose 3D-CRT and concurrent chemotherapy. Further studies may use these metrics in considering patients for these treatments.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=21477940&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.ijrobp.2011.01.056
dc.subjectAdult
dc.subjectAged
dc.subjectAnalysis of Variance
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectArea Under Curve
dc.subjectCarboplatin
dc.subjectCarcinoma, Non-Small-Cell Lung
dc.subjectChemoradiotherapy
dc.subjectDeoxycytidine
dc.subjectFemale
dc.subjectHumans
dc.subjectInduction Chemotherapy
dc.subjectLung
dc.subjectLung Neoplasms
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectOrgans at Risk
dc.subjectPaclitaxel
dc.subjectRadiotherapy Dosage
dc.subjectRadiotherapy Planning, Computer-Assisted
dc.subjectRadiotherapy, Conformal
dc.subjectNeoplasms
dc.subjectOncology
dc.titlePulmonary toxicity in Stage III non-small cell lung cancer patients treated with high-dose (74 Gy) 3-dimensional conformal thoracic radiotherapy and concurrent chemotherapy following induction chemotherapy: a secondary analysis of Cancer and Leukemia Group B (CALGB) trial 30105
dc.typeJournal Article
dc.source.journaltitleInternational journal of radiation oncology, biology, physics
dc.source.volume81
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/radiationoncology_pubs/51
dc.identifier.contextkey5020148
html.description.abstract<p>PURPOSE: Cancer and Leukemia Group B (CALGB) 30105 tested two different concurrent chemoradiotherapy platforms with high-dose (74 Gy) three-dimensional conformal radiotherapy (3D-CRT) after two cycles of induction chemotherapy for Stage IIIA/IIIB non-small cell lung cancer (NSCLC) patients to determine if either could achieve a primary endpoint of >18-month median survival. Final results of 30105 demonstrated that induction carboplatin and gemcitabine and concurrent gemcitabine 3D-CRT was not feasible because of treatment-related toxicity. However, induction and concurrent carboplatin/paclitaxel with 74 Gy 3D-CRT had a median survival of 24 months, and is the basis for the experimental arm in CALGB 30610/RTOG 0617/N0628. We conducted a secondary analysis of all patients to determine predictors of treatment-related pulmonary toxicity.</p> <p>METHODS AND MATERIALS: Patient, tumor, and treatment-related variables were analyzed to determine their relation with treatment-related pulmonary toxicity.</p> <p>RESULTS: Older age, higher N stage, larger planning target volume (PTV)1, smaller total lung volume/PTV1 ratio, larger V20, and larger mean lung dose were associated with increasing pulmonary toxicity on univariate analysis. Multivariate analysis confirmed that V20 and nodal stage as well as treatment with concurrent gemcitabine were associated with treatment-related toxicity. A high-risk group comprising patients with N3 disease and V20 >38% was associated with 80% of Grades 3-5 pulmonary toxicity cases.</p> <p>CONCLUSIONS: Elevated V20 and N3 disease status are important predictors of treatment related pulmonary toxicity in patients treated with high-dose 3D-CRT and concurrent chemotherapy. Further studies may use these metrics in considering patients for these treatments.</p>
dc.identifier.submissionpathradiationoncology_pubs/51
dc.contributor.departmentQuality Assurance Review Center
dc.contributor.departmentDepartment of Radiation Oncology
dc.source.pagese269-74


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