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dc.rights.licenseopenen_US
dc.contributor.authorHUCHET, Noemie
dc.contributor.authorPENEL, Nicolas
dc.contributor.authorBONVALOT, Sylvie
dc.contributor.authorTHARIAT, Juliette
dc.contributor.authorDUCIMETIERE, Francoise
dc.contributor.authorGIRAUD, Antoine
dc.contributor.authorTOULMONDE, Maud
dc.contributor.authorLE CESNE, Axel
dc.contributor.authorBLAY, Jean-Yves
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBELLERA, Carine
dc.date.accessioned2024-02-21T14:13:34Z
dc.date.available2024-02-21T14:13:34Z
dc.date.issued2024-01-19
dc.identifier.issn1758-8340en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/188299
dc.description.abstractEnBACKGROUND: Missing covariates are common in observational research and can lead to bias and loss of statistical power. Limited data regarding prognostic factors of survival outcomes of sarcomas in irradiated fields (SIF) are available. Because of the long lag time between irradiation of first cancer and scarcity of SIF, missing data are a critical issue when analyzing long-term outcomes. We assessed prognostic factors of overall (OS), progression-free (PFS), and metastatic-progression-free (MPFS) survivals in SIF using three methods to account for missing covariates. METHODS: We relied on the NETSARC French Sarcoma Group database, Cox (OS/PFS), and competitive hazards (MPFS) survival models. Covariates investigated were age, sex, histological subtype, tumor size, depth and grade, metastasis, surgery, surgical resection, surgeon's expertise, imaging, and neo-adjuvant treatment. We first applied multiple imputation (MI): observed data were used to estimate the missing covariate. With the missing-data modality approach, a category missing was created for qualitative variables. With the complete-case (CC) approach, analysis was restricted to patients without missing covariates. RESULTS: CC subjects (N = 167; 33%) presented more often with soft-tissue sarcoma (versus visceral sarcoma) and grade I-II tumors as compared to the 504 eligible cases. With MI (N = 504), factors associated with the worst outcome included metastasis (p = 0.04) and R1/R2 resection (p < 0.001) for OS; higher grade/non-gradable tumors (p = 0.002) and R1/R2 resection (p < 0.001) for PFS; and metastasis (p = 0.01) for M-PFS. The 'missing-data modality' approach (N = 504) led to different associations, including significance reached due to variables with the modality 'missing'. The CC analysis led to different results and reduced precision. CONCLUSION: The CC population was not representative of the eligible population, introducing bias, in addition to worst precision. The 'missing-data modality method' results in biased estimates in non-randomized studies, as outcomes may be related to variables with missing values. Appropriate statistical methods for missing covariates, for example, MI, should therefore be considered.
dc.description.sponsorshipDevelopment Cancer and Targeted Therapies - ANR-10-LABX-0061en_US
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subject.encompeting risks
dc.subject.enirradiation
dc.subject.ensarcoma
dc.subject.ensurvival analysis
dc.title.enHandling missing covariates in observational studies: an illustration with the assessment of prognostic factors of survival outcomes in soft-tissue or visceral sarcomas in irradiated fields (SIF)
dc.title.alternativeTher Adv Med Oncolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1177/17588359231220999en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed38249328en_US
dc.description.sponsorshipEuropeEuropean Clinical trials in Rare Sarcomas within an integrated translational trial networken_US
bordeaux.journalTherapeutic Advances in Medical Oncologyen_US
bordeaux.volume16en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamEPICENE_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Therapeutic%20Advances%20in%20Medical%20Oncology&amp;rft.date=2024-01-19&amp;rft.volume=16&amp;rft.eissn=1758-8340&amp;rft.issn=1758-8340&amp;rft.au=HUCHET,%20Noemie&amp;PENEL,%20Nicolas&amp;BONVALOT,%20Sylvie&amp;THARIAT,%20Juliette&amp;DUCIMETIERE,%20Francoise&amp;rft.genre=article


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