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. 2024 May 17;28(1):330. doi: 10.3892/ol.2024.14464

Table II.

Adverse events.

1st LEN (n=39) 2nd LEN (n=13)


Grade, n Grade, n


Events 1 2 3 4 All grades (%) 1 2 3 4 All grades (%) P-value
Leucopenia 5 7 1 0 13 (33.3) 2 1 1 0 4 (30.8) 0.864
Neutropenia 2 6 3 0 11 (28.2) 3 1 0 0 4 (30.8) 0.860
Platelet count decreased 17 10 1 0 28 (71.8) 5 3 1 0 9 (69.2) 0.860
Aspartate aminotransferase/alanine aminotransferase increased 17 1 0 0 18 (46.2) 7 0 3 0 10 (76.9) 0.016a
Blood bilirubin increased 10 6 2 0 18 (46.2) 2 3 0 0 5 (38.5) 0.629
Anemia 13 3 2 0 18 (46.2) 4 3 0 0 7 (53.8) 0.631
Diarrhea 5 0 1 0 6 (15.4) 3 1 0 0 4 (30.8) 0.244
Nausea 3 2 0 0 5 (12.8) 1 0 0 0 1 (7.7) 0.616
Vomiting 2 0 0 - 2 (5.1) 0 0 0 - 0 0.405
Fatigue 11 4 1 - 16 (41.0) 6 2 0 - 8 (61.5) 0.199
Proteinuria 0 11 4 - 15 (38.5) 2 0 3 - 5 (38.5) 1
Anorexia 11 2 1 0 14 (35.9) 5 0 0 0 5 (38.5) 0.868
Edema in limbs 7 0 0 - 7 (17.9) 5 0 0 - 5 (38.5) 0.128
Hypertension 8 4 2 0 14 (35.9) 1 0 0 0 1 (7.7) 0.052
Hand-foot-syndrome 4 4 0 - 8 (20.5) 4 1 0 - 5 (38.5) 0.196
Hoarseness 1 0 0 - 1 (2.6) 0 0 0 - 0 0.560
Rash 1 0 0 0 1 (2.6) 0 0 0 0 0 0.560
Musculoskeletal and connective tissue disorder 2 0 0 0 2 (5.1) 0 0 0 0 0 0.405
Hypothyroidism 2 3 0 0 5 (12.8) 3 3 0 0 6 (46.2) 0.011a
Epistaxis 1 0 0 0 1 (2.6) 0 0 0 0 0 0.560
Oral pain 2 0 0 - 2 (5.1) 0 0 0 - 0 0.405
Dizziness 1 0 0 - 1 (2.6) 0 0 0 - 0 0.560
Abdominal pain 2 0 0 - 2 (5.1) 0 0 0 - 0 0.405

Fisher's exact probability tests.

a

P<0.05. Atez/BV, atezolizumab/bevacizumab; LEN, lenvatinib; CPK, creatine kinase. 1st LEN is a group in which lenvatinib was used as the first-line treatment. 2nd LEN is a group in which atezolizumab plus bevacizumab was used as the first-line treatment and lenvatinib was used as the second-line treatment.