A prospective, multicenter study of caspofungin for the treatment of documented candida or aspergillus infections in pediatric patients

Theoklis E. Zaoutis, Hasan S. Jafri, Li Min Huang, Franco Locatelli, Asher Barzilai, Wolfram Ebell, William J. Steinbach, John Bradley, Jay M. Lieberman, Chih Cheng Hsiao, Nita Seibel, Hans Juergen Laws, Melinda Gamba, Maria Petrecz, Arlene F. Taylor, Kim M. Strohmaier, Joseph W. Chow, Nicholas A. Kartsonis, Angela L. Ngai

Research output: Contribution to journalArticle

Abstract

OBJECTIVE. We evaluated the safety, tolerability, and efficacy of caspofungin in pediatric patients with invasive aspergillosis, invasive candidiasis, or esophageal candidiasis. METHODS. This was a multicenter, prospective, open-label study in children 3 months to 17 years of age with proven or probable invasive aspergillosis, proven invasive candidiasis, or proven esophageal candidiasis. All of the patients received caspofungin 70 mg/m 2 on day 1, followed by 50 mg/m 2 per day (maximum: 70 mg/day), as primary or salvage monotherapy. Favorable response was defined as complete resolution of clinical findings and microbiologic (or radiographic/endoscopic) eradication (complete response) or significant improvement in these parameters (partial response). Efficacy was assessed at the end of caspofungin therapy in patients with a confirmed diagnosis who received ≥ 1 dose of caspofungin. The primary safety evaluation was the proportion of patients with clinical or laboratory drug-related adverse events. RESULTS. Of the 49 patients enrolled, 3 were <2 years of age, 30 were 2 to 11 years of age, and 16 were 12 to 17 years of age. Forty-eight patients had confirmed disease: invasive aspergillosis (10), invasive candidiasis (37), and esophageal candidiasis (1). Eight of 10 patients with invasive aspergillosis had pulmonary involvement; 34 of 37 patients with invasive candidiasis had candidemia. Caspofungin was given for 2 to 87 days. Success at end of therapy was achieved in 5 of 10 patients with invasive aspergillosis, 30 of 37 with invasive candidiasis, and 1 of 1 with esophageal candidiasis. One patient (invasive candidiasis) relapsed during the 28-day follow-up period. Drug-related clinical or laboratory adverse events occurred in 27% and 35% of patients, respectively. There were no serious drug-related adverse events or discontinuations of caspofungin because of toxicity. CONCLUSIONS. Caspofungin was generally well tolerated in pediatric patients aged 6 months through 17 years. Efficacy outcomes in patients with invasive aspergillosis or invasive candidiasis were consistent with previous adult studies in these indications.

Original languageEnglish
Pages (from-to)877-884
Number of pages8
JournalPediatrics
Volume123
Issue number3
DOIs
Publication statusPublished - Mar 2009

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caspofungin
Aspergillus
Candida
Multicenter Studies
Invasive Candidiasis
Prospective Studies
Pediatrics
Infection
Aspergillosis
Candidiasis
Therapeutics
Drug-Related Side Effects and Adverse Reactions
Invasive Pulmonary Aspergillosis
Candidemia

Keywords

  • Caspofungin
  • Echinocandin
  • Invasive aspergillosis
  • Invasive candidiasis
  • Pediatric patients

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

A prospective, multicenter study of caspofungin for the treatment of documented candida or aspergillus infections in pediatric patients. / Zaoutis, Theoklis E.; Jafri, Hasan S.; Huang, Li Min; Locatelli, Franco; Barzilai, Asher; Ebell, Wolfram; Steinbach, William J.; Bradley, John; Lieberman, Jay M.; Hsiao, Chih Cheng; Seibel, Nita; Laws, Hans Juergen; Gamba, Melinda; Petrecz, Maria; Taylor, Arlene F.; Strohmaier, Kim M.; Chow, Joseph W.; Kartsonis, Nicholas A.; Ngai, Angela L.

In: Pediatrics, Vol. 123, No. 3, 03.2009, p. 877-884.

Research output: Contribution to journalArticle

Zaoutis, TE, Jafri, HS, Huang, LM, Locatelli, F, Barzilai, A, Ebell, W, Steinbach, WJ, Bradley, J, Lieberman, JM, Hsiao, CC, Seibel, N, Laws, HJ, Gamba, M, Petrecz, M, Taylor, AF, Strohmaier, KM, Chow, JW, Kartsonis, NA & Ngai, AL 2009, 'A prospective, multicenter study of caspofungin for the treatment of documented candida or aspergillus infections in pediatric patients', Pediatrics, vol. 123, no. 3, pp. 877-884. https://doi.org/10.1542/peds.2008-1158
Zaoutis, Theoklis E. ; Jafri, Hasan S. ; Huang, Li Min ; Locatelli, Franco ; Barzilai, Asher ; Ebell, Wolfram ; Steinbach, William J. ; Bradley, John ; Lieberman, Jay M. ; Hsiao, Chih Cheng ; Seibel, Nita ; Laws, Hans Juergen ; Gamba, Melinda ; Petrecz, Maria ; Taylor, Arlene F. ; Strohmaier, Kim M. ; Chow, Joseph W. ; Kartsonis, Nicholas A. ; Ngai, Angela L. / A prospective, multicenter study of caspofungin for the treatment of documented candida or aspergillus infections in pediatric patients. In: Pediatrics. 2009 ; Vol. 123, No. 3. pp. 877-884.
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T1 - A prospective, multicenter study of caspofungin for the treatment of documented candida or aspergillus infections in pediatric patients

AU - Zaoutis, Theoklis E.

AU - Jafri, Hasan S.

AU - Huang, Li Min

AU - Locatelli, Franco

AU - Barzilai, Asher

AU - Ebell, Wolfram

AU - Steinbach, William J.

AU - Bradley, John

AU - Lieberman, Jay M.

AU - Hsiao, Chih Cheng

AU - Seibel, Nita

AU - Laws, Hans Juergen

AU - Gamba, Melinda

AU - Petrecz, Maria

AU - Taylor, Arlene F.

AU - Strohmaier, Kim M.

AU - Chow, Joseph W.

AU - Kartsonis, Nicholas A.

AU - Ngai, Angela L.

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N2 - OBJECTIVE. We evaluated the safety, tolerability, and efficacy of caspofungin in pediatric patients with invasive aspergillosis, invasive candidiasis, or esophageal candidiasis. METHODS. This was a multicenter, prospective, open-label study in children 3 months to 17 years of age with proven or probable invasive aspergillosis, proven invasive candidiasis, or proven esophageal candidiasis. All of the patients received caspofungin 70 mg/m 2 on day 1, followed by 50 mg/m 2 per day (maximum: 70 mg/day), as primary or salvage monotherapy. Favorable response was defined as complete resolution of clinical findings and microbiologic (or radiographic/endoscopic) eradication (complete response) or significant improvement in these parameters (partial response). Efficacy was assessed at the end of caspofungin therapy in patients with a confirmed diagnosis who received ≥ 1 dose of caspofungin. The primary safety evaluation was the proportion of patients with clinical or laboratory drug-related adverse events. RESULTS. Of the 49 patients enrolled, 3 were <2 years of age, 30 were 2 to 11 years of age, and 16 were 12 to 17 years of age. Forty-eight patients had confirmed disease: invasive aspergillosis (10), invasive candidiasis (37), and esophageal candidiasis (1). Eight of 10 patients with invasive aspergillosis had pulmonary involvement; 34 of 37 patients with invasive candidiasis had candidemia. Caspofungin was given for 2 to 87 days. Success at end of therapy was achieved in 5 of 10 patients with invasive aspergillosis, 30 of 37 with invasive candidiasis, and 1 of 1 with esophageal candidiasis. One patient (invasive candidiasis) relapsed during the 28-day follow-up period. Drug-related clinical or laboratory adverse events occurred in 27% and 35% of patients, respectively. There were no serious drug-related adverse events or discontinuations of caspofungin because of toxicity. CONCLUSIONS. Caspofungin was generally well tolerated in pediatric patients aged 6 months through 17 years. Efficacy outcomes in patients with invasive aspergillosis or invasive candidiasis were consistent with previous adult studies in these indications.

AB - OBJECTIVE. We evaluated the safety, tolerability, and efficacy of caspofungin in pediatric patients with invasive aspergillosis, invasive candidiasis, or esophageal candidiasis. METHODS. This was a multicenter, prospective, open-label study in children 3 months to 17 years of age with proven or probable invasive aspergillosis, proven invasive candidiasis, or proven esophageal candidiasis. All of the patients received caspofungin 70 mg/m 2 on day 1, followed by 50 mg/m 2 per day (maximum: 70 mg/day), as primary or salvage monotherapy. Favorable response was defined as complete resolution of clinical findings and microbiologic (or radiographic/endoscopic) eradication (complete response) or significant improvement in these parameters (partial response). Efficacy was assessed at the end of caspofungin therapy in patients with a confirmed diagnosis who received ≥ 1 dose of caspofungin. The primary safety evaluation was the proportion of patients with clinical or laboratory drug-related adverse events. RESULTS. Of the 49 patients enrolled, 3 were <2 years of age, 30 were 2 to 11 years of age, and 16 were 12 to 17 years of age. Forty-eight patients had confirmed disease: invasive aspergillosis (10), invasive candidiasis (37), and esophageal candidiasis (1). Eight of 10 patients with invasive aspergillosis had pulmonary involvement; 34 of 37 patients with invasive candidiasis had candidemia. Caspofungin was given for 2 to 87 days. Success at end of therapy was achieved in 5 of 10 patients with invasive aspergillosis, 30 of 37 with invasive candidiasis, and 1 of 1 with esophageal candidiasis. One patient (invasive candidiasis) relapsed during the 28-day follow-up period. Drug-related clinical or laboratory adverse events occurred in 27% and 35% of patients, respectively. There were no serious drug-related adverse events or discontinuations of caspofungin because of toxicity. CONCLUSIONS. Caspofungin was generally well tolerated in pediatric patients aged 6 months through 17 years. Efficacy outcomes in patients with invasive aspergillosis or invasive candidiasis were consistent with previous adult studies in these indications.

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KW - Invasive candidiasis

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