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Prospective Evaluation of Limited Stage Small Cell Lung Cancer (LS-SCLC) Fractionation Regimen Usage and Toxicity in a Large Statewide Quality Collaborative

dc.contributor.authorAllen, Steven G
dc.contributor.authorDragovic, Aleksandar F
dc.contributor.authorYin, Maggie
dc.contributor.authorBryant, Alex K
dc.contributor.authorPaximadis, Peter
dc.contributor.authorMatuszak, Martha
dc.contributor.authorSchipper, Matthew
dc.contributor.authorDess, Robert
dc.contributor.authorHayman, James
dc.contributor.authorPierce, Lori
dc.contributor.authorDominello, Michael
dc.contributor.authorKestin, Larry
dc.contributor.authorGrills, Inga
dc.contributor.authorMovsas, Benjamin
dc.contributor.authorJolly, Shruti
dc.contributor.authorBergsma, Derek
dc.contributor.authorConsortium, on behalf of the Michigan Radiation Oncology Quality
dc.coverage.spatialScottsdale, AZ
dc.date.accessioned2023-05-31T19:02:41Z
dc.date.available2023-05-31T19:02:41Z
dc.date.issued2023-04-24
dc.identifier.issn1879-8500
dc.identifier.issn1879-8519
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pubmed/37100388
dc.identifier.urihttps://hdl.handle.net/2027.42/176789en
dc.description.abstractPURPOSE: National guidelines on limited stage small cell lung cancer (LS-SCLC) treatment give preference to a hyperfractionated regimen of 45 Gy/30 fractions delivered twice-daily, however use of this regimen is uncommon compared to once-daily regimens. The purpose of this study was to characterize the LS-SCLC fractionation regimens used throughout a statewide collaborative, analyze patient and treatment factors associated with these regimens, and describe real-world acute toxicity profiles of once- and twice-daily RT regimens. METHODS AND MATERIALS: Demographic, clinical, and treatment data along with physician toxicity and patient-reported outcomes were prospectively collected by 29 institutions within the [quality consortium] between 2012 and 2021 for patients with LS-SCLC. We modeled the influence of RT fractionation and other patient-level variables clustered by treatment site on the odds of a treatment break specifically due to toxicity with multilevel logistic regression. Common Terminology Criteria for Adverse Events, version 4.0, incident Grade 2 or worse toxicity was longitudinally compared between regimens. RESULTS: There were 78 patients (15.6% overall) treated with twice-daily RT and 421 patients treated with once-daily RT. Patients receiving twice-daily RT were more likely to be married/living with someone (65% vs 51%, p=0.019) and to have no major comorbidities (24% vs 10%, p=0.017). Once-daily RT fractionation toxicity peaked during RT and twice-daily toxicity peaked within 1 month after RT. After stratifying by treatment site and adjusting for patient-level variables, once-daily treated patients had a 4.11 (95% confidence interval 1.31-12.87) higher odds of treatment break specifically due to toxicity than twice-daily treated patients. CONCLUSION: Hyperfractionation for LS-SCLC remains infrequently prescribed despite the lack of evidence demonstrating superior efficacy or lower toxicity of once-daily RT. With peak acute toxicity after RT and lower likelihood of a treatment break with twice-daily fractionation in real-word practice, providers may start utilizing hyperfractionated RT more frequently.
dc.format.mediumPrint-Electronic
dc.publisherElsevier
dc.subjectMichigan Radiation Oncology Quality Consortium
dc.titleProspective Evaluation of Limited Stage Small Cell Lung Cancer (LS-SCLC) Fractionation Regimen Usage and Toxicity in a Large Statewide Quality Collaborative
dc.typeConference Paper
dc.identifier.pmid37100388
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/176789/2/1-s2.0-S1879850023001145-main.pdf
dc.identifier.doi10.1016/j.prro.2023.04.007
dc.identifier.doihttps://dx.doi.org/10.7302/7638
dc.identifier.sourcePract Radiat Oncol
dc.description.versionPublished online
dc.date.updated2023-05-31T19:02:37Z
dc.identifier.orcid0000-0002-4129-1030
dc.identifier.orcid0000-0001-6728-4720
dc.identifier.orcid0000-0003-2331-3758
dc.identifier.orcid0000-0003-1391-5608
dc.identifier.orcid0000-0002-8174-5199
dc.identifier.orcid0000-0002-6293-4496
dc.description.filedescriptionDescription of 1-s2.0-S1879850023001145-main.pdf : Published version
dc.identifier.startpageS1879-8500(23)00114-5
dc.identifier.name-orcidAllen, Steven G
dc.identifier.name-orcidDragovic, Aleksandar F
dc.identifier.name-orcidYin, Maggie
dc.identifier.name-orcidBryant, Alex K
dc.identifier.name-orcidPaximadis, Peter
dc.identifier.name-orcidMatuszak, Martha; 0000-0002-4129-1030
dc.identifier.name-orcidSchipper, Matthew; 0000-0001-6728-4720
dc.identifier.name-orcidDess, Robert; 0000-0003-2331-3758
dc.identifier.name-orcidHayman, James; 0000-0003-1391-5608
dc.identifier.name-orcidPierce, Lori
dc.identifier.name-orcidDominello, Michael
dc.identifier.name-orcidKestin, Larry
dc.identifier.name-orcidGrills, Inga
dc.identifier.name-orcidMovsas, Benjamin
dc.identifier.name-orcidJolly, Shruti; 0000-0002-8174-5199
dc.identifier.name-orcidBergsma, Derek; 0000-0002-6293-4496
dc.identifier.name-orcidConsortium, on behalf of the Michigan Radiation Oncology Quality
dc.working.doi10.7302/7638en
dc.owningcollnameRadiation Oncology, Department of


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