key: cord-0687464-8smqivk0
authors: Mungmunpuntipantip, Rujittika; Wiwanitkit, Viroj
title: Hematological Malignancy Patients, COVID-19, and Favipiravir
date: 2021-12-07
journal: Turk J Haematol
DOI: 10.4274/tjh.galenos.2021.2021.0582
sha: 4b09a436b1d30d09e0b9d3f614a4eb4dc2b85243
doc_id: 687464
cord_uid: 8smqivk0

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We would like to share our ideas on the "Clinical Characteristics and Outcomes of COVID-19 in Turkish Hematological Malignancy Patients." As Civriz Bozdağ et al. [1] noted in that study: "Treatments with hydroxychloroquine alone or in combination with azithromycin were associated with a higher rate of mortality in comparison to favipiravir use". First, favipiravir is an antiviral drug proposed for management of COVID-19. Compared to other alternative drugs, including hydroxychloroquine and azithromycin, favipiravir should be more specifically applied in the management of viral infections. To determine the exact usefulness of favipiravir, clinical trials and observational studies are needed for assessment of drug efficacy and safety. Comparative studies between favipiravir and other therapies would also be useful and would yield more data on favipiravir. The report cited here is a good example of this. Another example is a previous comparative study of favipiravir therapy and other antiviral drugs [2] .

Regarding the effects of favipiravir, some additional considerations should be discussed. Other concurrent therapies, such as steroid medications, can also affect the clinical outcome [3] . Additional analysis of the possible effects of concurrent use of steroids with favipiravir, hydroxychloroquine, azithromycin, or their combination would be interesting. Additionally, whether the efficacy of the drug is associated with specific types and severities of hematological malignancies is a point for further research. The day of initiation of favipiravir treatment is also an important factor for therapeutic outcome [4] . According to a recent report by Doi et al.

[5], early and late administrations of favipiravir result in different clinical outcomes. More data on the exact period between onset of disease and start of favipiravir are required. Regarding the present report [1] , Civriz Bozdağ et al. [1] might consider additional factor analysis regarding the time effect for assessment of the effect of favipiravir. If future study designs are to be based on the current report of Civriz Bozdağ et al. [1] , it may be necessary to conduct an additional prospective study from the onset of COVID-19 to the start of favipiravir administration. In our study, we reported the clinical characteristics and outcomes of 340 adult and pediatric COVID-19 patients with hematological malignancies from March to November 2020. The aim of the study was to evaluate the factors related to severity and mortality of COVID-19 retrospectively; the study was not statistically designed to show the impact of treatment on outcomes. There was no approved treatment for COVID-19 so treatment plans in our country entailed hydroxychloroquine (HCQ) alone or in combination with azithromycin as initial treatment and favipiravir for further progress of pneumonia in follow-up. In the later months, favipiravir was introduced to the initial treatment schedule for COVID-19, which resulted in the formation of different treatment groups within our retrospective data.

In multivariate analysis related to mortality, besides hematological disease status, decreased life expectancy related to primary hematological disease, neutropenia, and admission to the intensive care unit, the type of COVID-19 treatment was a significant factor. Patients treated with HCQ alone had 4.9fold higher mortality risk in comparison to patients treated with favipiravir alone, while those treated with HCQ plus favipiravir had 2.0-fold risk and those treated with HCQ plus azithromycin had 2.1-fold risk. Favipiravir is an antiviral drug so a greater impact may be expected in comparison to HCQ. However, it should be kept in mind that the treatment policy in our country was changed after the negative results published on HCQ treatment. Furthermore, we did not have any other patients treated with different antiviral agents in our study.

For patients treated with favipiravir as the initial treatment, all were treated with the drug on the day of COVID-19 diagnosis, so we do not have a second group for a comparison of the impact of the timeline, unfortunately. Anticytokine treatments were administered based on individual centers' policies so the data were heterogenous for further analyses. We agree that prospective studies would better show the outcome differences between favipiravir and other antiviral therapies.

Clinical characteristics and outcomes of COVID-19 in Turkish hematological malignancy patients

The comparison of favipiravir and lopinavir/ritonavir combination in COVID-19 treatment

Outcome of early-stage combination treatment with favipiravir and methylprednisolone for severe COVID-19 pneumonia: a report of 11 cases

Early favipiravir treatment was associated with early defervescence in non-severe COVID-19 patients