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For researchers and clinicians following this issue, this is the central question in the upcoming FDA decision: is dysesthesia frequent and debilitating enough to justify a special mention in the indications, or even a 12 mg dose reserved for specific patients

20, 5271 (2014).CrossRefGoogle ScholarPubMed Liu, J., Zhang, B., Luo, Z., Ding, X., Li, J., Dai, L., Zhou, J., Zhao, X., Ye, J., and Cai, K.: Enzyme responsive mesoporous silica nanoparticles for targeted tumor therapy in vitro and in vivo