Knowledge of the classification of an anticancer agent as cytotoxic chemotherapy, (anti)hormonal agent, biological agent, targeted agent and/or immunotherapy
Knowledge of the specific mechanisms of action of an individual anticancer agent
Knowledge of the specific mechanisms of resistance that have been identified for an individual anticancer agent
Knowledge of key clinical pharmacology principles of individual anticancer agents, including absorption, distribution, metabolism and clearance/elimination (ADME)
Knowledge of the main clinical indications for an individual anticancer agent
Knowledge of the recommended dosing for an individual anticancer agent and how to adapt it to individual tolerability
Knowledge of food–drug interactions for an individual anticancer agent, especially as they relate to the use of oral anticancer therapy
Knowledge of drug–drug interactions, which include drug–herb and drug–nutritional supplement interactions, for an individual anticancer agent
Knowledge of the main side effects associated with an individual anticancer agent
Knowledge of the specific black-box warnings for an individual anticancer agent
Knowledge of dosing of an individual anticancer agent in the setting of liver and/or kidney dysfunction (see subsection 4.12)
Knowledge of specific considerations for an individual anticancer agent, such as potential interactions with the oral anticoagulants coumarin or warfarin, monitoring for signs and symptoms of fluid retention, close monitoring of complete blood counts (CBCs), monitoring of QT interval, monitoring for infusion reactions etc
Knowledge of the use of molecular biomarkers and specific diagnostic tests for the selection of targeted agents in the treatment of specific cancer types (see subsection 4.2)
Knowledge of newly registered anticancer agents and their indication