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Table 3 Severe (grade 3–4) acute toxicity during concurrent chemotherapy and late toxicity during follow up

From: Impact of cumulative cisplatin dose in childhood nasopharyngeal carcinoma based on neoadjuvant chemotherapy response in the intensity-modulated radiotherapy era: a real-world study

Adverse event

Entire cohort (n, %)

CC-CCD group (n, %)

P valuea

< 160 mg/m2

≥ 160 mg/m2

Acute toxicity (n = 132)

 

n = 52

n = 80

 

 Mucositis

57 (43.2)

21 (40.4)

36 (45.0)

0.719

 Nausea

23 (17.4)

10 (19.2)

13 (16.3)

0.648

 Leucopenia

35 (26.5)

14 (26.9)

21 (26.3)

0.996

 Neutropenia

18 (13.6)

9 (17.3)

9 (11.3)

0.437

 Anemia

5 (3.8)

1 (1.9)

4 (5.0)

0.648

 Thrombocytopenia

2 (1.5)

1 (1.9)

1 (1.3)

0.997

Late toxicity (n = 115)

 

n = 43

n = 72

 

 Xerostomia

11 (9.6)

5 (11.6)

6 (8.3)

0.723

 Ototoxicity

9 (7.8)

4 (9.3)

5 (6.9)

0.726

 Neck fibrosis

6 (5.2)

2 (4.7)

4 (5.6)

0.992

 Hypothyroidism

3 (2.6)

2 (4.7)

1 (1.4)

0.555

  1. CC-CCD cumulative cisplatin dose during concurrent chemoradiotherapy
  2. aP values were calculated using the chi-square test or Fisher exact test if indicated