In multivariable Cox regression analyses adjusting for known confounding prognostic factors (myometrial invasion, FIGO grade, and stage and molecular subtype), tumors with FGFR2b +/ FGFR2c − expression remained significantly associated with longer DSS (HR 0.37; 95% CI 0.153–0.872; LRTP <0.023) and OS (HR 0.71; 95% CI 0.409–0.921; LRTP <0.045) and showed a trend toward significance for PFS compared to FGFR2b −/ FGFR2c + (Table 3 ).
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Spatial expression of the FGFR2b splice isoform and its prognostic significance in endometrioid endometrial carcinoma.
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