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Table 6 Treatment-related toxicities after each cycle of topotecan and cyclophosphamide containing induction therapy

From: Clinical outcomes and prognostic factors to predict treatment response in high risk neuroblastoma patients receiving topotecan and cyclophosphamide containing induction regimen: a prospective multicenter study

 

Data

First cycle

Second cycle

Hospital stay (days)

Median (range)

7 (5–10)

5 (5–40)

Nadir period (days)

Median (range)

15 (10–20)

15 (10–20)

Readmission after chemotherapy

No

71 (66.4)

88 (82.2)

Ward

33 (30.8)

18 (16.8)

ICU

3 (2.8)

1 (0.9)

Febrile neutropenia

No

63 (58.9)

86 (80.4)

Yes

44 (41.1)

21 (19.6)

Mucositis

No

84 (78.5)

93 (86.9)

Yes

23 (21.5)

14 (13.1)

Diarrhea

No

102 (95.3)

103 (96.3)

Yes

5 (4.7)

4 (3.7)

Typhlitis

No

106 (99.1)

106 (99.1)

Yes

1 (0.9)

1 (0.9)

Renal dysfunction

No

106 (99.1)

106 (99.1)

Yes

1 (0.9)

1 (0.9)

Elevated liver enzymes

No

105 (98.1)

106 (99.1)

Yes

2 (1.9)

1 (0.9)

  1. Notes: Data are presented as number (%) for categorical variables