I corroborate an important experimental evidence reported by [Schuldt et al., PRL, 2016, 117, 197801] revealing the incapability of the current theoretical framework to fully describe the dynamics of semiflexible polymer solutions in the tightly-entangled concentration regime. These results have been endorsed here by means of previously published, but overlooked, data by [Tassieri et al., PRL, 2008, 101, 198301; Tassieri et al., Biophysical J., 2008, 94, 2170. The ensemble of information provides a strong evidence that the scaling law of the plateau modulus as function of polymer's concentration and persistence length, i.e. G 0 ∝ c α L β p , should have both the exponents positive; in contrast with all the existing predictions converging on similar values of α > 0 and β < 0. Hence, the need of new theoretical models able to better interpret the contribution of the polymer bending rigidity to the viscoelastic properties of the polymer network.