Appropriate informed consent procedures are crucial to preservation of patient autonomy and facilitation of shared decision making. According to the National Academy of Medicine, “regulations that govern the attainment of informed consent…are crucial to ensuring that medical care and research are conducted in an ethical manner and with the utmost respect for individual preferences and dignity.”
1 However, obtaining truly informed consent is a challenge in many medical settings, including cancer treatment, where the landscape of therapeutic options is increasingly complex and shifting. Informed consent for radiotherapy may be particularly difficult given its technical and abstract nature.
2 Despite the associated risks, radiotherapy is received by about half of patients with cancer,
3,4 and studies have shown that patients desire extensive information about their treatment and the associated adverse effects.
5 Recent research suggests that nearly half of patients initiating radiotherapy have heard frightening stories, heightening the need for optimal communication during the consent process.
6