Antifungal Prophylaxis in Acute Myeloid Leukemia: New Drugs, New Challenges?: Summary of the EHA Guideline on Antifungal Prophylaxis in Adult Patients With Acute Myeloid Leukemia Treated With Novel-targeted Therapies : HemaSphere

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Antifungal Prophylaxis in Acute Myeloid Leukemia: New Drugs, New Challenges?

Summary of the EHA Guideline on Antifungal Prophylaxis in Adult Patients With Acute Myeloid Leukemia Treated With Novel-targeted Therapies

Stemler, Jannik1,2,3; Cornely, Oliver A.1,2,3,4

Author Information
doi: 10.1097/HS9.0000000000000742
Erratum

Since the publication of the article entitled “Antifungal Prophylaxis in Acute Myeloid Leukemia: New Drugs, New Challenges? Summary of the EHA Guideline on Antifungal Prophylaxis in Adult Patients With Acute Myeloid Leukemia Treated With Novel-targeted Therapies” (HemaSphere. 2022;6(7):e742), a correction is needed for the correspondence information. The correct corresponding author name is Jannik Stemler. This has now been adjusted. The journal office apologizes for any inconvenience.

The changes have been made online: https://journals.lww.com/hemasphere/Fulltext/2022/07000/Antifungal_Prophylaxis_in_Acute_Myeloid_Leukemia_.5.aspx

HemaSphere. 6(7):e756, July 2022.

Patients with acute myeloid leukemia (AML) belong to the highest risk group for developing invasive fungal disease (IFD) at diagnosis or during treatment course. Relevant entities of IFD in this population include invasive candidiasis and candidemia mostly acquired through fungal translocation of commensal yeasts from the lumen of the gastrointestinal tract via the mucosal barrier, whereas invasive mold infections are acquired through airborne inhalation of fungal conidia, airway germination, and subsequent dissemination. These entities affect profoundly neutropenic patients. Therefore, triazole-based antifungal prophylaxis for mold coverage has been a cornerstone for clinical management in this patient population for decades, with results from randomized controlled trials (RCT) supporting its use in prevention of IFD and reducing mortality with low numbers-needed-to-treat.1,2

Although novel-targeted therapies have recently become available with promising data to improve the outcome of AML, their metabolism pathways interact with antifungals of the azole class. This poses significant challenges in patient management.3 Clinical questions at this crossroad comprise (i) if antifungal prophylaxis is to be implemented depending on novel agent and status of disease, (ii) the selection of antifungal agent and duration of its use, and (iii) the role of potential drug-drug interactions (DDI) for toxicity.4,5 The latter has been an upcoming issue in recent years as many novel available targeted therapies, like venetoclax, FLT3-inhibitors (midostaurin, gilteritinib, quizartinib, etc.), or IDH-inhibitors (ivosidenib, enasidenib) are substrates of the cytochrome p450 enzyme system to a varying extent, whereas triazole antifungals like posaconazole and voriconazole are potent inhibitors of this system.6

To address those questions, EHA gathered an expert group in 2019 to give recommendations for clinical management in cooperation with the Cochrane Haematology Group. For the resulting guideline, studies including all relevant novel-targeted agents and antifungal agents were reviewed, summarized and—depending on available studies—evidence-based or consensus-based recommendations were phrased.

Despite the obvious lack of high-quality studies assessing the use of antifungal prophylaxis in this specific setting, evidence-based recommendations were phrased for the hypomethylating agents (HMA) azacitidine and decitabine, as well as for venetoclax, gemtuzumab-ozogamicin, and midostaurin. Consensus-based statements were given for dasatinib, gilteritinib, glasdegib, idasanutlin, ivosidenib, lestaurtinib, and sorafenib, generally with low to very low certainty of evidence.7 For some AML drugs, no recommendation was possible due to scarce data and other agents, such as etrenapopt, olutasidenib, and others, were not considered since even the clinical trial data for safety and efficacy had not been available when this guideline was endeavored.

Generally, the use of antifungal prophylaxis is indicated in fit patients with AML during remission-induction chemotherapy (RIC), as recommended by former guidelines, also if combined with novel agents, for example, FLT3-inhibitors, especially in the context of long-lasting neutropenia.8-10 Since incidence of IFD in patients with AML not treated with intensive RIC has long been suggested to be lower, treating physicians do not consider this a scenario to administer antifungal prophylaxis. However, retrospective studies have shown an IFD incidence of up to 8%, being high enough to consider administering prophylaxis to prevent disease and premature death from IFD.11 In monotherapy settings, for example, with gilteritinib in relapsed/refractory AML, where duration of neutropenia cannot be estimated or is due to the underlying disease status, antifungal prophylaxis is also recommended. The only situation with robust underlying data from clinical studies to support dose reduction is the treatment with a combination of HMA and venetoclax with a recommendation to administer antifungal prophylaxis with a triazole and reduce the venetoclax dose by at least 75% with real-life data showing similar durations of neutropenia and thrombocytopenia as compared to administration of venetoclax without an azole.12 However, several retrospective studies show that potential DDI can play a role and their impact is not yet fully defined, such as in the case of midostaurin and gilteritinib. Further clinical concepts and their investigation under real-life conditions need to determine their use to support dose adaptations of the AML agent and the administration or omission of antifungal prophylaxis.13–15 Administration of other prophylactic antifungal agents, such as echinocandins, is more and more often considered in case of potential DDI. However, for these agents evidence is sparse and they are not lincensed for this indication in patients with AML and through their daily IV administration are a less feasible option for the outpatient setting in which many patients with orally administered targeted AML therapies are treated. Therefore, the strongest recommendation for antifungal prophylaxis remains for a mold-active triazole-based approach.1,7,9

If the recommendation was “either for or against antifungal prophylaxis,” this should guide the treating physician to taking the decision context-dependent, that is, according to the patient’s individual scenario, such as expected duration of neutropenia, history of IFD or local epidemiology of IFD.

The published recommendations also have limitations that remain a future challenge in the context of diversifying treatment settings for AML, emerging fungal pathogens and antifungal resistance, and different management approaches to prevent IFD. The clinical setting of a combination of any novel AML agent and their impact on development of IFD was not considered. Furthermore, the guideline’s scope was narrowed to mainly evaluate antifungal medication for prophylaxis and to respond concerns regarding potential DDI emphasizing the pharmacological perspective. Other approaches to reduce the risk of IFD, including general infection control measures like hand hygiene compliance, bundle-based care protocols for central venous access devices or reduction of environmental fungal conidia exposure, were not discussed. As a more general remark, antifungal stewardship principles should be implemented in any patient receiving an antifungal to determine the appropriate duration of exposure.

The EHA guidance also includes a research agenda. Further investigations in the field may comprise RCTs to evaluate efficacy of antifungal prophylaxis in patients with AML not treated with intensive RIC, as well as the assessment of real-life utilization of antifungal prophylaxis in patients with AML. The incidence of IFD in this high-risk population remains not well-defined and should be assessed in registries. Drug metabolization and thereby cytochrome p450-associated potential DDI including polymorphisms in the individual patient may gain importance for determination of the optimal cancer management. In this context, therapeutic drug monitoring (TDM) may play an increasing role to assess clinically relevant DDI by monitoring drug levels of both the antifungal, where TDM in a therapeutic setting is already a standard-of-care, and the antileukemic drugs. Further, this may even enable clinicians to adapt and personalize the dose according to measured level to finally optimize therapeutic effect and reduce toxicity of both drugs and thereby harnessing the maximum benefit for the individual patient.

Table 1. - Summary of Recommendations Regarding Antifungal Prophylaxis for Clinically Relevant Antileukemic Drugs
Drug Clinical Setting AFP Recommendation Evidence-Based or Consensus-Based Recommendation Comment
5-Azacitidine Induction and maintenance, generally combined with bcl-2 inhibitors Conditional for AFP Evidence-based with low certainty of evidence AFP should be considered in heavily pretreated patients, as secondary prophylaxis in patients with previous IFI and patients with long-lasting neutropenia.
Decitabine Induction and maintenance, generally combined with bcl-2 inhibitors Conditional for AFP Consensus-based Data regarding incidence and potential benefit of AFP was also extrapolated from patients treated with azacitidine.
Enasidenib Monotherapy or combination therapy with RIC or other agents No recommendation Consensus-based No recommendation was given due to limited clinical use and documentation of IFI.
Close monitoring for potential DDI and QTc interval.
Gemtuzumab-Ozogamicin During RIC in combination with intensive chemotherapy Conditional for AFP Evidence-based with low certainty of evidence Strong recommendation for AFP during RIC.
Gilteritinib Monotherapy in relapsed or refractoy AML Either for/against AFP Consensus-based In monotherapy setting, no benefit of AFP was documented.
Triazole AFP should be considered in heavily pretreated patients.
Glasdegib Monotherapy or in combination with LDAC Conditional against AFP Consensus-based Close monitoring for potential DDI and QTc interval.
Ivosidenib Monotherapy or combination therapy with RIC or other agents Either for/against AFP Consensus-based Conditional recommendation to reduce the dose to 250mg/day if concomitant use to strong CYP43A4 inhibitors.
Close monitoring for potential DDI and QTc interval.
Midostaurin During RIC in combination with intensive chemotherapy or as maintenance monotherapy Conditional for AFP Evidence-based with low certainty of evidence Strong recommendation for AFP during RIC.
Individual decision for or against antifungal prophylaxis when administered as monotherapy.
Close monitoring for potential DDI and QTc interval.
Sorafenib Maintenance monotherapy or during RIC in combination with intensive chemotherapy Conditional for AFP Consensus-based Strong recommendation for triazoles during RIC treatment.
Venetoclax Induction and maintenance in combination with hypomethylating agents or other drugs Conditional for AFP Evidence-based with low certainty of evidence Prefer AFP with triazoles during induction treatment. Reduce venetoclax dose to 70mg when using posaconazole or voriconazole concomitantly.
Quizartinib During RIC in combination with intensive chemotherapy Conditional for AFP Consensus-based Strong recommendation for AFP during RIC with a dose reduction of quizartinib if triazole prophylaxis is used.
In monotherapy setting, recommendation against AFP.
AML = acute myeloid leukemia; AFP = antifungal prophylaxis; DDI = drug-drug interactions; HMA = hypomthylating agents; IFI = invasive fungal infection; LDAC = low-dose cytarabine;RIC = remission-induction chemotherapy.

DISCLOSURES

JS has received research grants by the Ministry of Education and Research (BMBF) and Basilea Pharmaceuticals Inc.; has received speaker honoraria by Pfizer Inc.; and has received travel grants by German Society for Infectious Diseases (DGI e.V.) and Meta-Alexander Foundation. OAC reports grants or contracts from Amplyx, Basilea, BMBF, Cidara, DZIF, EU-DG RTD (101037867), F2G, Gilead, Matinas, MedPace, MSD, Mundipharma, Octapharma, Pfizer, Scynexis; Consulting fees from Abbvie, Amplyx, Biocon, Biosys, Cidara, Da Volterra, Gilead, Matinas, MedPace, Menarini, Molecular Partners, MSG-ERC, Noxxon, Octapharma, Pardes, PSI, Scynexis, Seres; Honoraria for lectures from Abbott, Al-Jazeera Pharmaceuticals, Astellas, Grupo Biotoscana/United Medical/Knight, Hikma, MedScape, MedUpdate, Merck/MSD, Mylan, Pfizer; Payment for expert testimony from Cidara; Participation on a Data Safety Monitoring Board or Advisory Board from Actelion, Allecra, Cidara, Entasis, IQVIA, Janssen, MedPace, Paratek, PSI, Pulmocide, Shionogi; A patent at the German Patent and Trade Mark Office (DE 10 2021 113 007.7); Other interests from DGHO, DGI, ECMM, ISHAM, MSG-ERC, Wiley.

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Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the European Hematology Association.