“…Among true interval BCs, triple-negative tumours were more frequently observed in fatty (<25% density) than in denser breasts ( p <0.001). FNs and occult interval BCs had similar phenotypic characteristics to screen-detected cancers.Renart-Vicens 26
| Interval vs. screen-detected BCs from Girona Health Region screening program 2000–06. | Interval BCs had significantly higher proportions of advanced stage disease (14% vs. 1%), larger tumours (5.4% vs. 2.3%), high-grade tumours (38% vs. 23%), and higher number of metastatic nodes (13.5% vs. 7.7%) than screen-detected BCs. | Interval BCs were non-significantly more likely to be triple-negative, and less likely to be luminal A tumours than screen-detected BCs. |
Boyd 11
| Interval vs. screen-detected BCs sourced from three case–control studies nested in screened populations, by density measured with various methods. | Interval BCs had significantly larger (average) maximum tumour diameter for each measure of density (percent mammographic density, dense and non-dense areas) than screen-detected BCs. | – |
Caldarella 43
| Interval vs. screen-detected BCs, Florence population screening program 2004–05. | Stage at diagnosis was more advanced for interval BCs than screen-detected BCs based on pT distribution (pT 2+ 25.8% vs. 10.4%, p < 0.001) and pN distribution (pN 1+ 41% vs. 29%, p = 0.032). | Relative to screen-detected BC, triple-negative BCs were over-represented, and luminal A (ER/PR positive, HER2 negative) BCs were under-represented among interval BCs |
Payne 39
| Interval vs. screen-detected BCs from Nova Scotia screening program 1991–2004. | Interval BCs were more likely to be node-positive, to be larger tumours, to have higher grade, and to show lymphovascular invasion than screen-detected BCs (all p < 0.001). | Interval BCs less likely to be ER positive than screen-detected BCs ( p = 0.002). |
Kalager 46
| Interval BC in the Norwegian screening program vs. BCs in same time frame in population not yet invited to screening (non-screened women). | Interval BCs had slightly higher proportions of larger tumours (>20 mm), stage II rather than stage I cancer, invasive lobular histology, and negative (non-metastatic) axillary nodes, than BCs in non-screened women (distributions for these variables differed at p < 0.001). | – |
Caumo 44
| Interval vs. screen-detected vs. clinical BCs occurring in the absence of screening, Verona mammography screening program 2000–06 and Veneto cancer registry. | Interval BCs had more aggressive features than screen-detected BCs for pT ( p < 0.001), pN ( p < 0.001), and tumour grade distributions ( p = 0.007). Interval BCs had similar prognostic features as clinical BCs based on pT, pN and grade distributions (all p > 0.05). | Interval BCs less likely to be ER-positive (77% vs. 91%, p < 0.001) and PR-positive (61% vs. 82%, p < 0.001) than screen-detected BCs. |
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