Grading of joint and muscle related adverse events*
irAE | Grade 1 | Grade 2 | Grade 3 | Grades 4–5 |
---|---|---|---|---|
Arthralgia1 | Mild pain | Moderate pain; limiting instrumental ADL | Severe pain; limiting self-care ADL | n.a. |
Arthritis2 | Mild pain with inflammation erythema, or joint swelling | Moderate pain associated with signs of inflammation, erythema, or joint swelling; limiting instrumental ADL | Severe pain associated with signs of inflammation, erythema, or joint swelling; irreversible joint damage | n.a. |
Joint effusion3 | Asymptomatic, clinical or diagnostic observation only; no intervention needed | Symptomatic; limiting ADL | Severe symptoms; limiting self-care ADL; invasive intervention indicated | n.a. |
Myalgia4 | Mild pain | Moderate pain; limiting instrumental ADL | Severe pain; limiting self-care ADL | n.a. |
Myositis5 | Mild pain | Moderate pain associated with weakness; pain limiting instrumental ADL | Pain associated with severe weakness; limiting self-care ADL | Life-threatening consequences; urgent intervention indicated |
*: Extracted from National Cancer Institute. Common terminology criteria for adverse events (CTCAE) v5.0; 2017. Available from (page 95–98): https://ctep.cancer.gov/protocoldevelopment/electronic_applications/docs/CTCAE_v5_Quick_Reference_5x7.pdf. 1: a disorder characterized by a sensation of marked discomfort in a joint. 2: a disorder characterized by inflammation involving a joint. 3: a disorder characterized by excessive fluid in a joint, usually as a result of joint inflammation. 4: a disorder characterized by marked discomfort sensation originating from a muscle or group of muscles. 5: a disorder characterized by inflammation involving the skeletal muscles. CTCAE v5.0 incorporates certain elements of the MedDRA terminology. For further details on MedDRA refer to the MedDRA MSSO Web site (https://www.meddra.org/). MedDRA® the Medical Dictionary for Regulatory Activities terminology is the international medical terminology developed under the auspices of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). irAE: immune-related adverse event; ADL: activity of daily living; n.a.: not applicable