This, in turn, enabled the analysis of the relationship between bFGF level and tumor sensitivity to the antiproliferation effect of paclitaxel in subgroups of tumors with different pathobiological properties; the results show better correlations in four pathobiological subgroups (late stages, positive p53 staining, negative aFGF staining, higher-than-median bFGF level), compared to all other groups. Here, FGF1 is linked to neoplasm.