Skip to main content
. Author manuscript; available in PMC: 2024 Oct 1.
Published in final edited form as: Lancet Oncol. 2023 Sep 8;24(10):1083–1093. doi: 10.1016/S1470-2045(23)00388-1

Table 2.

Acute adverse events regardless of attribution (CTCAE v4.0)

Adverse Event Conventional (N=41) Hypofractionation (N=41)
Grade 1 Grade 2 Grade 3 Grade 4 Grade 5 Total Grade 1 Grade 2 Grade 3 Grade 4 Grade 5 Total
Breast infection 1 (2.4%) 1 (2.4%) 2 (4.9%) 3 (7.3%) 3 (7.3%)
Esophagitis 5 (12.2%) 5 (12.2%) 6 (14.6%) 2 (4.9%) 8 (19.5%)
Breast edema 9 (22.0%) 9 (22.0%) 4 (9.8%) 4 (9.8%)
Skin hyperpigmentation 30 (73.2%) 2 (4.9%) 32 (78.0%) 19 (46.3%) 2 (4.9%) 21 (51.2%)
Edema limbs 5 (12.2%) 5 (12.2%) 1 (2.4%) 1 (2.4%) 2 (4.9%)
Dermatitis radiation 20 (48.8%) 19 (46.3%) 39 (95.1%) 33 (80.5%) 7 (17.1%) 40 (97.6%)
Stroke 1 (2.4%) 1 (2.4%)
Non-cardiac chest pain 2 (4.9%) 2 (4.9%) 2 (4.9%) 2 (4.9%)
Joint range of motion decreased 11 (26.8%) 11 (26.8%) 7 (17.1%) 7 (17.1%)

Adverse events of grade 1–2 occurring in at least 10% of patients or grade 3–5 occurring in any patient across both groups are reported. Note: No grade 4 events were reported in either arm and no grade 5 events in the conventional arm