Table 2.
Study Design | Follow-Up in Months, Median, Range |
Toxicity ≥ Grade 3 %, Weighted Median |
Most Common irAEs |
---|---|---|---|
AntiPD1/antiPD-L1 + SABR | 14.0 (2,9–33) |
14,5% | Pneumonitis, asthenia, breakthrough pain, colitis, neurological and hepatic toxicity |
Anti CTLA4 + SABR | 20.0 (2–38) |
26,0% | Pneumonitis, fatigue, liver enzymes increase, colitis and neurological |
AntiPD1/AntiPD-L1 alone | 11.0 (7–14,5) |
10,8% | Pneumonia, increased aspartate aminotransferase, skin reactions, pneumonitis, neutropenia, anemia, thrombocytopenia, diarrhea |
IT = immunotherapy; RT = radiotherapy; irAEs = immune-related adverse events.