Intravenous itraconazole for prophylaxis of systemic fungal infections in patients with acute myelogenous leukemia and high‐risk myelodysplastic syndrome undergoing induction chemotherapy

BACKGROUND Systemic fungal infections remain the leading cause of mortality in patients with newly diagnosed acute myelogenous leukemia (AML) and high‐risk myelodysplastic syndrome (MDS). The objective of the current study was to determine whether intravenous itraconazole (I.V. ITRA) reduced the inc...

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Veröffentlicht in:Cancer 2004-02, Vol.100 (3), p.568-573
Hauptverfasser: Mattiuzzi, Gloria N., Kantarjian, Hagop, O'Brien, Susan, Kontoyiannis, Dimitrios P., Giles, Francis, Zhou, Xian, Lim, JoAnn, Bekele, B. Nebiyou, Faderl, Stefan, Cortes, Jorge, Pierce, Sherry, Leitz, Gerhard J., Raad, Issam, Estey, Elihu
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container_end_page 573
container_issue 3
container_start_page 568
container_title Cancer
container_volume 100
creator Mattiuzzi, Gloria N.
Kantarjian, Hagop
O'Brien, Susan
Kontoyiannis, Dimitrios P.
Giles, Francis
Zhou, Xian
Lim, JoAnn
Bekele, B. Nebiyou
Faderl, Stefan
Cortes, Jorge
Pierce, Sherry
Leitz, Gerhard J.
Raad, Issam
Estey, Elihu
description BACKGROUND Systemic fungal infections remain the leading cause of mortality in patients with newly diagnosed acute myelogenous leukemia (AML) and high‐risk myelodysplastic syndrome (MDS). The objective of the current study was to determine whether intravenous itraconazole (I.V. ITRA) reduced the incidence of probable/proven fungal infections in this group of patients, and compare the results with those of a historic control group treated with fluconazole plus itraconazole capsules (F+I). METHODS Patients with AML and high‐risk MDS who underwent induction chemotherapy received 200 mg of i.v. itraconazole over 60 minutes every 12 hours during the first 2 days followed by 200 mg given i.v. once daily. RESULTS One hundred patients were enrolled, 96 of whom were evaluable. Approximately 48% of the patients in the group of patients treated with IV ITRA as well as in the F+I group completed prophylaxis. Nine patients (9%) in the study group developed either proven/probable fungal infections (Candida glabrata in 5 patients, C. tropicalis in 1 patient, C krusei in 1 patient, and Fusarium in 2 patients) compared with 3 patients (4%) with proven fungal infection in the historic control group (C. tropicalis in 1 patient and Aspergillus in 2 patients). There were no significant differences noted between the two groups with regard to the percentage of patients who developed proven/probable or possible fungal infection as well as with regard to survival. These results also were obtained after adjusting for relevant prognostic factors (creatinine and bilirubin). The most common toxicity encountered with the use of IV ITRA was NCI Grade 3‐4 hyperbilirubinemia (6%). CONCLUSIONS Despite its theoretic advantages, the authors found no evidence that IV ITRA is superior to itraconazole capsules, at least when the latter is combined with fluconazole. Cancer 2004. © 2003 American Cancer Society. Systemic fungal infections remain the leading cause of mortality in patients with newly diagnosed acute myelogenous leukemia and high‐risk myelodysplastic syndrome. In the current study, the authors attempted to determine whether intravenous itraconazole reduced the incidence of probable/proven fungal infections in this group of patients and compared the results with those of a historic control group that was treated with fluconazole plus itraconazole capsules.
doi_str_mv 10.1002/cncr.11930
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Nebiyou ; Faderl, Stefan ; Cortes, Jorge ; Pierce, Sherry ; Leitz, Gerhard J. ; Raad, Issam ; Estey, Elihu</creator><creatorcontrib>Mattiuzzi, Gloria N. ; Kantarjian, Hagop ; O'Brien, Susan ; Kontoyiannis, Dimitrios P. ; Giles, Francis ; Zhou, Xian ; Lim, JoAnn ; Bekele, B. Nebiyou ; Faderl, Stefan ; Cortes, Jorge ; Pierce, Sherry ; Leitz, Gerhard J. ; Raad, Issam ; Estey, Elihu</creatorcontrib><description>BACKGROUND Systemic fungal infections remain the leading cause of mortality in patients with newly diagnosed acute myelogenous leukemia (AML) and high‐risk myelodysplastic syndrome (MDS). The objective of the current study was to determine whether intravenous itraconazole (I.V. ITRA) reduced the incidence of probable/proven fungal infections in this group of patients, and compare the results with those of a historic control group treated with fluconazole plus itraconazole capsules (F+I). METHODS Patients with AML and high‐risk MDS who underwent induction chemotherapy received 200 mg of i.v. itraconazole over 60 minutes every 12 hours during the first 2 days followed by 200 mg given i.v. once daily. RESULTS One hundred patients were enrolled, 96 of whom were evaluable. Approximately 48% of the patients in the group of patients treated with IV ITRA as well as in the F+I group completed prophylaxis. Nine patients (9%) in the study group developed either proven/probable fungal infections (Candida glabrata in 5 patients, C. tropicalis in 1 patient, C krusei in 1 patient, and Fusarium in 2 patients) compared with 3 patients (4%) with proven fungal infection in the historic control group (C. tropicalis in 1 patient and Aspergillus in 2 patients). There were no significant differences noted between the two groups with regard to the percentage of patients who developed proven/probable or possible fungal infection as well as with regard to survival. These results also were obtained after adjusting for relevant prognostic factors (creatinine and bilirubin). The most common toxicity encountered with the use of IV ITRA was NCI Grade 3‐4 hyperbilirubinemia (6%). CONCLUSIONS Despite its theoretic advantages, the authors found no evidence that IV ITRA is superior to itraconazole capsules, at least when the latter is combined with fluconazole. Cancer 2004. © 2003 American Cancer Society. Systemic fungal infections remain the leading cause of mortality in patients with newly diagnosed acute myelogenous leukemia and high‐risk myelodysplastic syndrome. In the current study, the authors attempted to determine whether intravenous itraconazole reduced the incidence of probable/proven fungal infections in this group of patients and compared the results with those of a historic control group that was treated with fluconazole plus itraconazole capsules.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.11930</identifier><identifier>PMID: 14745874</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Analysis of Variance ; Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage ; Biological and medical sciences ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Female ; fluconazole ; fungal infections ; Fungemia - drug therapy ; Fungemia - prevention &amp; control ; Hematologic and hematopoietic diseases ; Humans ; Infusions, Intravenous ; itraconazole ; Itraconazole - administration &amp; dosage ; leukemia ; Leukemia, Myeloid, Acute - diagnosis ; Leukemia, Myeloid, Acute - drug therapy ; Leukemia, Myeloid, Acute - mortality ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Logistic Models ; Male ; Medical sciences ; Middle Aged ; Multivariate Analysis ; Myelodysplastic Syndromes - diagnosis ; Myelodysplastic Syndromes - drug therapy ; Myelodysplastic Syndromes - mortality ; Primary Prevention - methods ; Probability ; Prognosis ; prophylaxis ; Proportional Hazards Models ; Prospective Studies ; Remission Induction ; Risk Assessment ; Survival Analysis ; Treatment Outcome ; Tumors</subject><ispartof>Cancer, 2004-02, Vol.100 (3), p.568-573</ispartof><rights>Copyright © 2003 American Cancer Society</rights><rights>2004 INIST-CNRS</rights><rights>Copyright 2003 American Cancer Society.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3910-4d4e1575989bc60560222ccd7d7e1fc68e1c56f58a3ebd5d113f489593fc9083</citedby><cites>FETCH-LOGICAL-c3910-4d4e1575989bc60560222ccd7d7e1fc68e1c56f58a3ebd5d113f489593fc9083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcncr.11930$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcncr.11930$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,1434,27929,27930,45579,45580,46414,46838</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15413045$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14745874$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mattiuzzi, Gloria N.</creatorcontrib><creatorcontrib>Kantarjian, Hagop</creatorcontrib><creatorcontrib>O'Brien, Susan</creatorcontrib><creatorcontrib>Kontoyiannis, Dimitrios P.</creatorcontrib><creatorcontrib>Giles, Francis</creatorcontrib><creatorcontrib>Zhou, Xian</creatorcontrib><creatorcontrib>Lim, JoAnn</creatorcontrib><creatorcontrib>Bekele, B. Nebiyou</creatorcontrib><creatorcontrib>Faderl, Stefan</creatorcontrib><creatorcontrib>Cortes, Jorge</creatorcontrib><creatorcontrib>Pierce, Sherry</creatorcontrib><creatorcontrib>Leitz, Gerhard J.</creatorcontrib><creatorcontrib>Raad, Issam</creatorcontrib><creatorcontrib>Estey, Elihu</creatorcontrib><title>Intravenous itraconazole for prophylaxis of systemic fungal infections in patients with acute myelogenous leukemia and high‐risk myelodysplastic syndrome undergoing induction chemotherapy</title><title>Cancer</title><addtitle>Cancer</addtitle><description>BACKGROUND Systemic fungal infections remain the leading cause of mortality in patients with newly diagnosed acute myelogenous leukemia (AML) and high‐risk myelodysplastic syndrome (MDS). The objective of the current study was to determine whether intravenous itraconazole (I.V. ITRA) reduced the incidence of probable/proven fungal infections in this group of patients, and compare the results with those of a historic control group treated with fluconazole plus itraconazole capsules (F+I). METHODS Patients with AML and high‐risk MDS who underwent induction chemotherapy received 200 mg of i.v. itraconazole over 60 minutes every 12 hours during the first 2 days followed by 200 mg given i.v. once daily. RESULTS One hundred patients were enrolled, 96 of whom were evaluable. Approximately 48% of the patients in the group of patients treated with IV ITRA as well as in the F+I group completed prophylaxis. Nine patients (9%) in the study group developed either proven/probable fungal infections (Candida glabrata in 5 patients, C. tropicalis in 1 patient, C krusei in 1 patient, and Fusarium in 2 patients) compared with 3 patients (4%) with proven fungal infection in the historic control group (C. tropicalis in 1 patient and Aspergillus in 2 patients). There were no significant differences noted between the two groups with regard to the percentage of patients who developed proven/probable or possible fungal infection as well as with regard to survival. These results also were obtained after adjusting for relevant prognostic factors (creatinine and bilirubin). The most common toxicity encountered with the use of IV ITRA was NCI Grade 3‐4 hyperbilirubinemia (6%). CONCLUSIONS Despite its theoretic advantages, the authors found no evidence that IV ITRA is superior to itraconazole capsules, at least when the latter is combined with fluconazole. Cancer 2004. © 2003 American Cancer Society. Systemic fungal infections remain the leading cause of mortality in patients with newly diagnosed acute myelogenous leukemia and high‐risk myelodysplastic syndrome. In the current study, the authors attempted to determine whether intravenous itraconazole reduced the incidence of probable/proven fungal infections in this group of patients and compared the results with those of a historic control group that was treated with fluconazole plus itraconazole capsules.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Analysis of Variance</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</subject><subject>Biological and medical sciences</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>fluconazole</subject><subject>fungal infections</subject><subject>Fungemia - drug therapy</subject><subject>Fungemia - prevention &amp; control</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Infusions, Intravenous</subject><subject>itraconazole</subject><subject>Itraconazole - administration &amp; dosage</subject><subject>leukemia</subject><subject>Leukemia, Myeloid, Acute - diagnosis</subject><subject>Leukemia, Myeloid, Acute - drug therapy</subject><subject>Leukemia, Myeloid, Acute - mortality</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Myelodysplastic Syndromes - diagnosis</subject><subject>Myelodysplastic Syndromes - drug therapy</subject><subject>Myelodysplastic Syndromes - mortality</subject><subject>Primary Prevention - methods</subject><subject>Probability</subject><subject>Prognosis</subject><subject>prophylaxis</subject><subject>Proportional Hazards Models</subject><subject>Prospective Studies</subject><subject>Remission Induction</subject><subject>Risk Assessment</subject><subject>Survival Analysis</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1q3TAQhUVpaG7TbvoARZtuCk4lS7q2l-XSn0BoIWSRndGVRrYaWTKSndRZ5RH6Qn2ZPkmV-EJ2Wc0MfOccmIPQO0pOKSHlJ-VVPKW0YeQF2lDSVAWhvHyJNoSQuhCcXR2j1yn9ymdVCvYKHVNecVFXfIP-nvkpyhvwYU7Y5lUFL--CA2xCxGMMY784-dsmHAxOS5pgsAqb2XfSYesNqMkGn6Uej3Ky4KeEb-3UY6nmCfCwgAvd6u5gvs5qiaXXuLdd_-_-T7TpeoX0kkYn05Td0-J1DAPg2WuIXbC-y_56fozCqochTD1EOS5v0JGRLsHbwzxBl1-_XO6-F-c_v53tPp8XijWUFFxzoKISTd3s1ZaILSnLUild6QqoUdsaqBJbI2rJYK-FppQZXjeiYUY1pGYn6ONqq2JIKYJpx2gHGZeWkvahgvahgvaxggy_X-Fx3g-gn9DDzzPw4QDIpKQzUXpl0xMnOGWEi8zRlbu1DpZnItvdj93FGv4f8kSm4w</recordid><startdate>20040201</startdate><enddate>20040201</enddate><creator>Mattiuzzi, Gloria N.</creator><creator>Kantarjian, Hagop</creator><creator>O'Brien, Susan</creator><creator>Kontoyiannis, Dimitrios P.</creator><creator>Giles, Francis</creator><creator>Zhou, Xian</creator><creator>Lim, JoAnn</creator><creator>Bekele, B. Nebiyou</creator><creator>Faderl, Stefan</creator><creator>Cortes, Jorge</creator><creator>Pierce, Sherry</creator><creator>Leitz, Gerhard J.</creator><creator>Raad, Issam</creator><creator>Estey, Elihu</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20040201</creationdate><title>Intravenous itraconazole for prophylaxis of systemic fungal infections in patients with acute myelogenous leukemia and high‐risk myelodysplastic syndrome undergoing induction chemotherapy</title><author>Mattiuzzi, Gloria N. ; Kantarjian, Hagop ; O'Brien, Susan ; Kontoyiannis, Dimitrios P. ; Giles, Francis ; Zhou, Xian ; Lim, JoAnn ; Bekele, B. 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Nebiyou</au><au>Faderl, Stefan</au><au>Cortes, Jorge</au><au>Pierce, Sherry</au><au>Leitz, Gerhard J.</au><au>Raad, Issam</au><au>Estey, Elihu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intravenous itraconazole for prophylaxis of systemic fungal infections in patients with acute myelogenous leukemia and high‐risk myelodysplastic syndrome undergoing induction chemotherapy</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2004-02-01</date><risdate>2004</risdate><volume>100</volume><issue>3</issue><spage>568</spage><epage>573</epage><pages>568-573</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>BACKGROUND Systemic fungal infections remain the leading cause of mortality in patients with newly diagnosed acute myelogenous leukemia (AML) and high‐risk myelodysplastic syndrome (MDS). The objective of the current study was to determine whether intravenous itraconazole (I.V. ITRA) reduced the incidence of probable/proven fungal infections in this group of patients, and compare the results with those of a historic control group treated with fluconazole plus itraconazole capsules (F+I). METHODS Patients with AML and high‐risk MDS who underwent induction chemotherapy received 200 mg of i.v. itraconazole over 60 minutes every 12 hours during the first 2 days followed by 200 mg given i.v. once daily. RESULTS One hundred patients were enrolled, 96 of whom were evaluable. Approximately 48% of the patients in the group of patients treated with IV ITRA as well as in the F+I group completed prophylaxis. Nine patients (9%) in the study group developed either proven/probable fungal infections (Candida glabrata in 5 patients, C. tropicalis in 1 patient, C krusei in 1 patient, and Fusarium in 2 patients) compared with 3 patients (4%) with proven fungal infection in the historic control group (C. tropicalis in 1 patient and Aspergillus in 2 patients). There were no significant differences noted between the two groups with regard to the percentage of patients who developed proven/probable or possible fungal infection as well as with regard to survival. These results also were obtained after adjusting for relevant prognostic factors (creatinine and bilirubin). The most common toxicity encountered with the use of IV ITRA was NCI Grade 3‐4 hyperbilirubinemia (6%). CONCLUSIONS Despite its theoretic advantages, the authors found no evidence that IV ITRA is superior to itraconazole capsules, at least when the latter is combined with fluconazole. Cancer 2004. © 2003 American Cancer Society. Systemic fungal infections remain the leading cause of mortality in patients with newly diagnosed acute myelogenous leukemia and high‐risk myelodysplastic syndrome. In the current study, the authors attempted to determine whether intravenous itraconazole reduced the incidence of probable/proven fungal infections in this group of patients and compared the results with those of a historic control group that was treated with fluconazole plus itraconazole capsules.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>14745874</pmid><doi>10.1002/cncr.11930</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Aged, 80 and over
Analysis of Variance
Antineoplastic Combined Chemotherapy Protocols - administration & dosage
Biological and medical sciences
Dose-Response Relationship, Drug
Drug Administration Schedule
Female
fluconazole
fungal infections
Fungemia - drug therapy
Fungemia - prevention & control
Hematologic and hematopoietic diseases
Humans
Infusions, Intravenous
itraconazole
Itraconazole - administration & dosage
leukemia
Leukemia, Myeloid, Acute - diagnosis
Leukemia, Myeloid, Acute - drug therapy
Leukemia, Myeloid, Acute - mortality
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
Logistic Models
Male
Medical sciences
Middle Aged
Multivariate Analysis
Myelodysplastic Syndromes - diagnosis
Myelodysplastic Syndromes - drug therapy
Myelodysplastic Syndromes - mortality
Primary Prevention - methods
Probability
Prognosis
prophylaxis
Proportional Hazards Models
Prospective Studies
Remission Induction
Risk Assessment
Survival Analysis
Treatment Outcome
Tumors
title Intravenous itraconazole for prophylaxis of systemic fungal infections in patients with acute myelogenous leukemia and high‐risk myelodysplastic syndrome undergoing induction chemotherapy
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