சுருக்கம்

Challenges in clinical trial design for recurrent glioblastoma

Katharine A McNeill, Howard A Fine

Glioblastomas are rare tumors but aggressive and often incurable. Since clinical trial enrollment is limited by the relative rarity of the disease, clinical trials should be well designed so that advances are made efficiently. The field has been dominated by smaller Phase II studies since they provide the initial screening of drug efficacy. These studies are prone to issues of selection bias, inappropriate historic controls and confounding clinical variables. There are also issues specific to glioblastoma, including the difficulty in interpreting radiographic responses in the setting of treatment effects and agents that affect vascular permeability and the difficulty of performing pharmacokinetic and pharmacodynamic studies given the relative inaccessibility of the CNS compartment. These barriers have also hindered the development of radiographic and molecular biomarkers. As we move into the era of personalized medicine, it is increasingly important to address these issues in the design of clinical trials.

மறுப்பு: இந்த சுருக்கமானது செயற்கை நுண்ணறிவு கருவிகளைப் பயன்படுத்தி மொழிபெயர்க்கப்பட்டது மற்றும் இன்னும் மதிப்பாய்வு செய்யப்படவில்லை அல்லது சரிபார்க்கப்படவில்லை