TABLE 1.
Toxicity: CTCAE | Pneumonitis % | Oesophagitis % | ||
Any grade | Grade 3–4 | Any grade | Grade 3–4 | |
PROCLAIM: standard therapy [96] | 10.7 | 2.6 | 50.7 | 20.6 |
RTOG 0617: 60 Gy [97] | Acute 11.1; late 9.8 | Acute 5.5; late 1.2 | 45.1 | 6.9 |
RTOG 0617: 74 Gy [97] | Acute 14.5; late 3.9 | Acute 3.4; late 1.1 | 54.1 | 17 |
KCSG-LU05–04: CRT phase [98] | 2.4 | 0 | 79.3 | 9.5 |
CONVERT: LD-SCLC, once daily [99] | Acute 22.4; late 32.6 | Acute 1.6; late 2.6 | Acute 74; late 18.5 | Acute 19.1; late 1.7 |
CONVERT: LD-SCLC, twice daily [99] | Acute 22; late 31 | Acute 1.6; late 2.4 | Acute 81.1; late 11.7 | Acute 18.5; late 0 |
PACIFIC: durvalumab [15] | 33.9 | 3.4 | ||
PACIFIC: placebo [15] | 24.8 | 2.6 | ||
NICOLAS: nivolumab [100] | 42.5 | 10.4 | 27.5 | 6.5 |
CTCAE: Common Terminology Criteria for Adverse Events; CRT: chemoradiotherapy; LD-SCLC: limited disease small cell lung cancer.