Breakthrough invasive fungal infections on isavuconazole prophylaxis in hematologic malignancy & hematopoietic stem cell transplant patients

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作者
Khatri, Akshay M. [1 ]
Natori, Yoichiro [2 ,3 ,9 ,10 ]
Anderson, Anthony [4 ]
Jabr, Ra'ed [5 ]
Shah, Shreya A. [4 ]
Natori, Akina [6 ]
Chandhok, Namrata S. [7 ]
Komanduri, Krishna [8 ]
Morris, Michele I. [2 ]
Camargo, Jose F. [2 ]
Raja, Mohammed [2 ]
机构
[1] UnityPoint Hlth Des Moines, Dept Med, Div Infect Dis, Des Moines, IA USA
[2] Univ Miami, Miller Sch Med, Dept Med, Div Infect Dis, Miami, FL 33136 USA
[3] Jackson Hlth Syst, Miami Transplant Inst, Miami, FL USA
[4] Sylvester Comprehens Canc Ctr, Dept Pharm, Miami, FL USA
[5] Mayo Clin Hlth Syst Eau Claire, Dept Med, Div Infect Dis, Miami, FL USA
[6] Univ Miami, Miller Sch Med, Dept Med, Div Med Oncol, Miami, FL 33136 USA
[7] Univ Miami, Miller Sch Med, Dept Med, Div Hematol, Miami, FL 33136 USA
[8] Univ Calif San Francisco, Dept Med, Div Hematol & Oncol, San Francisco, CA 94143 USA
[9] Miami Transplant Inst, Div Infect Dis, 1801 NW 9th Ave,Suite 733, Miami, FL USA
[10] Univ Miami, Miller Sch Med, 1801 NW 9th Ave,Suite 733, Miami, FL 33136 USA
关键词
breakthrough infection; fungal infection; hematopoietic stem cell transplant; Isavuconazole; prophylaxis; ANTIFUNGAL PROPHYLAXIS; FLUCONAZOLE; POSACONAZOLE; VORICONAZOLE; PREVENTION; RECIPIENTS; TRIAL;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BackgroundIsavuconazole (ISA) is a newer antifungal used in patients with history of hematologic malignancies and hematopoietic transplant and cellular therapies (HM/TCT). Although it has a more favorable side-effect profile, breakthrough invasive fungal infections (bIFIs) while on ISA have been reported.MethodsIn this single-center retrospective study evaluating HM/TCT patients who received prophylactic ISA for >= 7 days, we evaluated the incidence and potential risk factors for bIFIs.ResultsWe evaluated 106 patients who received prophylactic ISA. The patients were predominantly male (60.4%) with median age of 65 (range: 21-91) years. Acute myeloid leukemia (48/106, 45.3%) was the most common HM, with majority having relapsed and/or refractory disease (43/106, 40.6%) or receiving ongoing therapy (38/106, 35.8%).Nineteen patients (17.9%) developed bIFIs-nine proven [Fusarium (3), Candida (2), Mucorales plus Aspergillus (2), Mucorales (1), Colletotrichum (1)], four probable invasive pulmonary Aspergillus, and six possible infections. Twelve patients were neutropenic for a median of 28 (8-253) days prior to bIFI diagnosis. ISA levels checked within 7 days of bIFI diagnosis (median: 3.65 mu g/mL) were comparable to industry-sponsored clinical trials.All-cause mortality among the bIFI cases was 47.4% (9/19).We also noted clinically significant cytomegalovirus co-infection in 5.3% (1/19). On univariate analysis, there were no significant differences in baseline comorbidities and potential risk factors between the two groups.ResultsWe evaluated 106 patients who received prophylactic ISA. The patients were predominantly male (60.4%) with median age of 65 (range: 21-91) years. Acute myeloid leukemia (48/106, 45.3%) was the most common HM, with majority having relapsed and/or refractory disease (43/106, 40.6%) or receiving ongoing therapy (38/106, 35.8%).Nineteen patients (17.9%) developed bIFIs-nine proven [Fusarium (3), Candida (2), Mucorales plus Aspergillus (2), Mucorales (1), Colletotrichum (1)], four probable invasive pulmonary Aspergillus, and six possible infections. Twelve patients were neutropenic for a median of 28 (8-253) days prior to bIFI diagnosis. ISA levels checked within 7 days of bIFI diagnosis (median: 3.65 mu g/mL) were comparable to industry-sponsored clinical trials.All-cause mortality among the bIFI cases was 47.4% (9/19).We also noted clinically significant cytomegalovirus co-infection in 5.3% (1/19). On univariate analysis, there were no significant differences in baseline comorbidities and potential risk factors between the two groups.ResultsWe evaluated 106 patients who received prophylactic ISA. The patients were predominantly male (60.4%) with median age of 65 (range: 21-91) years. Acute myeloid leukemia (48/106, 45.3%) was the most common HM, with majority having relapsed and/or refractory disease (43/106, 40.6%) or receiving ongoing therapy (38/106, 35.8%).Nineteen patients (17.9%) developed bIFIs-nine proven [Fusarium (3), Candida (2), Mucorales plus Aspergillus (2), Mucorales (1), Colletotrichum (1)], four probable invasive pulmonary Aspergillus, and six possible infections. Twelve patients were neutropenic for a median of 28 (8-253) days prior to bIFI diagnosis. ISA levels checked within 7 days of bIFI diagnosis (median: 3.65 mu g/mL) were comparable to industry-sponsored clinical trials.All-cause mortality among the bIFI cases was 47.4% (9/19).We also noted clinically significant cytomegalovirus co-infection in 5.3% (1/19). On univariate analysis, there were no significant differences in baseline comorbidities and potential risk factors between the two groups.ConclusionISA prophylaxis was associated with a significant cumulative incidence of bIFIs. Despite the appealing side-effect and drug-interaction profile of ISA, clinicians must be vigilant about the potential risk for bIFIs.image In this single center retrospective study, we evaluated the incidence of breakthrough invasive fungal infections (bIFIs) in patients with hematologic malignancies and recipients of hematopoietic stem cell transplant and cellular therapies on isavuconazole prophylaxis. We noted bIFIs in 17.9%, with no potential risk factors for infection identified on univariate analysis.#image
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