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Table 2 TRAEs

From: A pilot study of multi-antigen stimulated cell therapy-I plus camrelizumab and apatinib in patients with advanced bone and soft-tissue sarcomas

 

All patients (N = 19)

Group by administration schedule of MASCT-I

Schedule-I group (N = 9)

Schedule-II group (N = 10)

Grade 1–2

Grade 3

Grade 4

Grades 1–2

Grade 3

Grade 4

Grades 1–2

Grade 3

Grade 4

Any

8 (42.1%)

10 (52.6%)

1 (5.3%)

5 (55.6%)

4 (44.4%)

0

3 (30.0%)

6 (60.0%)

1 (10.0%)

Neutrophil count decreased

10 (52.6%)

3 (15.8%)

1 (5.3%)

4 (44.4%)

1 (11.1%)

0

6 (60.0%)

2 (20.0%)

1 (10.0%)

Hypertriglyceridemia

13 (68.4%)

1 (5.3%)

0

7 (77.8%)

1 (11.1%)

0

6 (60.0%)

0

0

Proteinuria

12 (63.2%)

1 (5.3%)

0

5 (55.6%)

0

0

7 (70.0%)

1 (10.0%)

0

Hypothyroidism

12 (63.2%)

0

0

5 (55.6%)

0

0

7 (70.0%)

0

0

Hypercholesterolemia

10 (52.6%)

1 (5.3%)

0

5 (55.6%)

0

0

5 (50.0%)

1 (10.0%)

0

WBC count decreased

10 (52.6%)

1 (5.3%)

0

3 (33.3%)

0

0

7 (70.0%)

1 (10.0%)

0

Anemia

10 (52.6%)

1 (5.3%)

0

5 (55.6%)

0

0

5 (50.0%)

1 (10.0%)

0

Blood bilirubin increased

10 (52.6%)

0

0

5 (55.6%)

0

0

5 (50.0%)

0

0

Platelet count decreased

10 (52.6%)

0

0

2 (22.2%)

0

0

8 (80.0%)

0

0

Diarrhea

10 (52.6%)

0

0

4 (44.4%)

0

0

6 (60.0%)

0

0

Hypertension

7 (36.8%)

2 (10.5%)

0

2 (22.2%)

2 (22.2%)

0

5 (50.0%)

0

0

PPE syndrome

7 (36.8%)

0

0

3 (33.3%)

0

0

4 (40.0%)

0

0

AST increased

6 (31.6%)

0

0

4 (44.4%)

0

0

2 (20.0%)

0

0

Rash

6 (31.6%)

0

0

2 (22.2%)

0

0

4 (40.0%)

0

0

GGT increased

4 (21.1%)

1 (5.3%)

0

3 (33.3%)

0

0

1 (10.0%)

1 (10.0%)

0

Hyperuricemia

5 (26.3%)

0

0

2 (22.2%)

0

0

3 (30.0%)

0

0

Headache

5 (26.3%)

0

0

3 (33.3%)

0

0

2 (20.0%)

0

0

Pyrexia

5 (26.3%)

0

0

1 (11.1%)

0

0

4 (40.0%)

0

0

Stomatitis

3 (15.8%)

1 (5.3%)

0

1 (11.1%)

1 (11.1%)

0

2 (20.0%)

0

0

ALT increased

4 (21.1%)

0

0

2 (22.2%)

0

0

2 (20.0%)

0

0

RCCEP

4 (21.1%)

0

0

1 (11.1%)

0

0

3 (30.0%)

0

0

Liver injury

3 (15.8%)

0

0

2 (22.2%)

0

0

1 (10.0%)

0

0

Blood LDH increased

3 (15.8%)

0

0

0

0

0

3 (30.0%)

0

0

Pruritus

3 (15.8%)

0

0

2 (22.2%)

0

0

1 (10.0%)

0

0

Feeling cold

3 (15.8%)

0

0

3 (33.3%)

0

0

0

0

0

  1. Data are n (%). Data presented for TRAEs of any grade occurring in at least 20% of patients in either group and all TRAEs of grade 3 or 4 in either group. No grade 5 TRAE occurred. TRAEs are listed in descending order of frequency in the total patient population
  2. TRAE, Treatment-related adverse event; WBC, White blood cell; PPE, Palmar-plantar erythrodysesthesia; AST, Aspartate aminotransferase; GGT, Gamma-glutamyl transferase; ALT, Alanine aminotransferase; RCCEP, Reactive cutaneous capillary endothelial proliferation; LDH, Lactate dehydrogenase