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Table 1 Randomized multicentre clinical trials of antifungal therapy in patients with candidaemia or invasive candidiasis

From: Bench-to-bedside review: Candida infections in the intensive care unit

 

Pappas et al. [30]

Mora-Duarte et al. [32]

Kuse et al. [34]

Reboli et al. [35]

Kullberg et al. [33]

Rex et al. [31]

 

Micafungin

Micafungin

Caspofungin

Caspofungin

Amphotericin B deoxycholate

Micafungin

Liposomal amphotericin B

Anidulafungin

Fluconazole

Voriconazole

Amphotericin B deoxycholate followed by fluconazole

Fluconazole

Amphotericin B deoxycholate

Daily dose

100 mga

150 mga

70 mg load, followed by 50 mga

70 mg load, followed by 50 mga

0.6 to 0.7 mg/kga

100 mg

3 mg/kg

200 mg load, followed by 100 mga

800 mg load, followed by 400 mga

6 mg/kg twice daily day 1, followed by 3 mg/kg twice daily

0.7 to 1 mg/kg, day 3 to 7 iv/oral. Fluconazole 400 mg

400 mgb

0.5 to0.6 mg/kg

Number of patients

191

199

188

114

125

264

267

132

129

272

131

113

111

Mean APACHE II score

14.9

14.7

13.8

14.8

15.4

15.8

15.6

15.0

14.4

13.8

14.7

16

16

Neutrophil count <500/mm3

11.5%

8.5%

5.9%

12.8%

8.7%

13%

10%

2%

3%

Exclusion criterion

Exclusion criterion

Exclusion criterion

Exclusion criterion

Candida spp.

   C. albicans

48.2%

51.3%

44.1%

35.6%

54.1%

42%

44%

64%

59%

43%

21%

68%

61%

   Non-albicans

54.5%

51.3%

60.6%

64.4%

45.9%

62%

59%

43%

50%

61%

50%

32%

39%

C. glabrata

14.7%

17.1%

17.6%

12.8%

9.2%

11%

7.4%

16%

25%

15%

17%

12.6%

10.6%

C. krusei

4.2%

4.0%

2.1%

4%

0.9%

3%

3.5%

NR

NR

2%

1%

1.9%

1%

Site of infection

   Blood only

85.3%

84.4%

85.6%

82.6%

79.1%

84%

86%

91%

87%

96%

96%

70%

74%

   Blood and other site

NR

NR

NR

4.6%

3.5%

NR

NR

3%

3%

4%

4%

30%

26%

   Other site only

14.7%

15.1%

13.8%

12.8%

17.4%

16%

14%

6%

9%

NR

NR

NR

NR

Days of therapy

14 (median)

14(median)

14 (median)

12.1 (mean)

11.7 (mean)

15 (median)

15 (median)

15.9 (mean)

14.4 (mean)

15 (median)

15 (median)

18 (mean)

17 (mean)

Success of therapyc

   At end of iv therapy

76.4%

71.4%

72.3%

73.4%

61.7%

74.1%

69.6%

75.6%

60.2%

70%

74%

74%

83%

   C. glabrata infectiond

85.7%

88.2%

66.7%

76.9%

80%

82.6%e

80.0%e

75%

60%

33%f

33%f

NR

NR

   Neutropeniad

81.8%

52.9%

63.6%

50%

40%

59.4%

56.0%

NR

NR

NR

NR

NR

NR

Drug-related toxicityg

   Adverse eventsh

22%

22.8%

23.8%

42.1%

75.2%

43.2%

50.9%

24.4%i

26.4%i

46%

57%

NR

NR

   Therapy discontinuation

2.5%

3.0%

3.6%

2.6%

23.2%

4.9%

9.0%

NR

NR

6%

5%

2.9%i

3.8%i

  1. aSwitch to oral fluconazole (400 mg) possible after 10 days of intravenous therapy. bSwitch to oral fluconazole (400 mg) possible after 7 days of intravenous therapy. cModified intention-to-treat analyses, if not specified otherwise. dAt end of study drug administration, if not specified otherwise. e Per protocol analyses. f Response at 12-week follow-up visit. gIntention-to-treat analyses, if not specified otherwise. hClinical event and/or laboratory abnormality. iModified intention-to-treat analyses. APACHE, Acute Physiology and Chronic Health Evaluation; iv, intravenous; NR, not reported.